Άρθρα στον επιστημονικό τύπο

 

Το χρονικό διάστημα από το 2005 ώς το 2012 έγιναν 238 επιστημονικές δημοσιεύσεις από τους επιστήμονες του Ι.Υ.Π. 

 

 

  1. AKMAN O., KARADIMAS C., GYFTODIMOU Y., GRIGORIADOU M., KOKOTAS H., KONSTANTINIDOU A., ANNINOS H., PATSOURIS E., THAKER H., KAPLAN J., BESHARAT I., HATZIKONSTANTINOU K., FOTOPOULOS S., DIMAURO S., and PETERSEN M. (2006) PRENATAL DIAGNOSIS OF GLYCOGEN STORAGE DISEASE TYPE IV. PRENATAL DIAGNOSIS. 26, 951-955.
  2. ALTARESCU G., ZIMRAN A., MICHELAKAKIS H., and ELSTEIN D. (2005) TNF-αLEVELS AND TNF-αGENE POLYMORPHISM IN TYPE I GAUCHER DISEASE. CYTOKINE. 31, 149-152.
  3. ARGYRIOU A., DERMENTZAKIS G., PAPASILEKAS T., MORAITOU M., STAMBOULIS E., VEKRELLIS K., MICHELAKAKIS H., and STEFANIS L. (2012) INCREASED DIMERIZATION OF ALPHA-SYNUCLEIN IN ERYTHROCYTES IN GAUCHER DISEASE AND AGING. NEUROSCIENCE LETTERS. (Epub ahead of print).
  4. ARVANITIDOU V., VOSKAKI I., TRIPSIANIS G., ATHANASOPOULOU H., TSALKIDIS A., PHILIPPIDIS S., SCHULPIS K., and ANDROULAKIS I. (2006) SERUM COPPER AND ZINC CONCENTRATIONS IN HELTHY CHILDREN AGED 3-14 YEARS IN GREECE. BIOLOGICAL TRACE ELEMENT RESEARCH. 115, 1-12.
  5. ARVANITIDOU V., VOSKAKI I., TRIPSIANIS G., ATHANASOPOULOU H., TSILKIDIS A., FILIPPIDIS S., SCHULPIS K., and ANDROULAKIS I. (2007) SERUM COPPER AND ZINC CONSENTRATIONS IN HEALTHY CHILDREN AGED 3-14 YEARS IN GREECE. BIOLOGICAL TRACE ELEMENT RESEARCH. 115, 1-12.
  6. ATTILAKOS A. and ANTONIADOU I. (2005) REPLACING MERCURY SPHYGMOMANOMETER IN PAEDIATRIC CLINICAL PRACTICE: IS THERE A NEED FOR A CONSENSUS CONFERENCE? ARCH DIS CHILD. 90(6), 654.
  7. ATTILAKOS A., PAPAKONSTANTINOU E., SCHULPIS K., VOUDRIS K., KATSAROU E., MASTROYIANNI S. and GAROUFI A. (2006) EARLY EFFECT OF SODIUM VALPROATE AND CARBAMAZEPINE MONOTHERAPY ON HOMOCYSTEINE METABOLISM IN CHILDREN WITH EPILEPSY. EPILEPSY RESEARCH. 71, 229-232.
  8. BADA E. and SOKOU K. (2006) EVALUATING THE DEVELOPMENT IN HEALTH-PROMOTING SCHOOLS IN GREECE: 1992-2006. W.H.O. EUROPEAN COMMISION AND COUNSIL OF EUROPE. NETWORK NEWS THE EUROPEAN NETWORK OF HEALTH PROMOTIGN SCHOOLS. 10, 24-26.
  9. BADA E. (2006) GREEK ROMA SOCIAL PERFORMANCE, RESISTANCE AND CONFLICT RESOLUTION: THE CASE OF A ROMA TRIAL. JOURNAL OF ROMANI STUDIES. 16(2), 153-167.
  10. BLAU N., BELANGER-QUINTANA A., DEMIRKOL M., FEILLET F., GIOVANNINI M., MAcDONALD A., TREFZ F., VAN SPRONSEN F., and CONTRIBUTING EUROPEAN PKU CENTERS (2010) MANAGEMENT OF PHENYLKETONURIA IN EUROPE: SURVEY RESULTS FROM 19 COUNTRIES. MOLECULAR GENETICS AND METABOLISM. 99, 109-115.
  11. BUGGE M., COLLINS A., HERTZ J., EIBERG H., LUNDSTEEN C., BRANDT C., BAK M., HANSEN C., D. DELOZIER C., LESPINASSE J., TRANEBJAERG L., HAHNEMANN J., RASMUSSEN K., BRUUN-PETERSEN G., DUPREZ L., TOMMERUP N., and PETERSEN M. (2007) NON-DISJUNCTION OF CHROMOSOME 13. HUMAN MOLECULAR GENETICS. 16(16), 2004-2010.
  12. BUGGE M., DELOZIER-BLANCHET C., BAK M., BRANDT C., HERTZ J.M., BIEDER NIELSEN J., DUPREZ L., and PETERSEN M. (2005) TRISOMY 13 DUE TO REA(13q;13q) IS CAUSED BY i(13) AND NOT ROB (13;13) (q10;q10) IN THE MAJORITY OF CASES. AMERICAN JOURNAL OF MEDICAL GENETICS. 132A, 310-313.
  13. BUGIANI M., GYFTODIMOU Y., TSIMPOUKA P., LAMANTEA E., KATZAKI E., D'ADAMO P., NAKOU S., GEORGOUDI N., GRIGORIADOU M., TSINA E., KABOLIS N., MILANI D., PANDELIA E., KOKOTAS H., GASPARINI P., GIANNOULIA-KARANTANA A., RENIERI A., ZEVIANI M., and PETERSEN M.B. (2008) COHEN SYNDROME RESULTING FROM A NOVEL LARGE INTRAGENIC COH1 DELETION SEGREGATING IN AN ISOLATED GREEK ISLAND POPULATION. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 146A, 2221-2226. 
  14. CHALMERS R., BAIN M., MICHELAKAKIS H., ZSCHOCKE J., and ILES R. (2006) DIAGNOSIS AND MANAGEMENT OF TRIMETHYLAMINURIA (FMO3 DEFICIENCY) IN CHILDREN. J INHERIT METAB DIS. 29, 162-172.
  15. CHATZIKYRIAKIDOU A., LOUIZOU E., DEDOUSIS G., BISCEGLIA L., MICHELAKAKIS H., and GEOGRIOU I. (2008) AN OVERVIEW OF SLC3A1 AND SLC7A9 MUTATIONS IN GREEK CYSTINURIA PATIENTS. MOLECULAR GENETICS AND METABOLISM. 95(3), 192-193.
  16. CONSTANTINOU M., PAPAKONSTANTINOU E., SPRAUL M., SEVASTIADOU S., COSTALOS C., KOUPPARIS M., SCHULPIS K., TSANTILI-KAKOULIDOU A., and MIKROS E. (2005) 1H NMR-BASED METABONOMICS FOR THE DIAGNOSIS OF INBORN ERRORS OF METABOLISM IN URINE. ANALYTIKA CHIMICA ACTA. 542, 169-177.
  17. DI PERNA M., LOUIZOU E., FISCHETTI L., DEDOUSSIS G., STANZIALE P., MICHELAKAKIS H., ZELANTE L., PRAS E., and BISCEGLIA L. (2008) TWENTY-FOUR NOVEL MUTATIONS IDENTIFIED IN A COHORT OF 85 PATIENTS BY DIRECT SEQUENCING OF THE SLC3A1 AND SLC7A9 CYSTINURIA GENES. GENETIC TESTING. 12(3), 351-356.
  18. DIMITRIOU E., MORAITOU M., TROUNGOS C., SCHULPIS K., and MICHELAKAKIS H. (2010) GAUCHER DISEASE: FREQUENCY OF THE N370S MUTATION IN THE GREEK POPULATION. CLIN GENET. 78, 195-196.
  19. DIMITRIOU E., VERHOEK M., ALTUN S., KARABATSOS F., MORAITOU M., YOUSSEF J., BOOT R., SARAFIDOU J., KARAGIORGA M., AERTS H., and MICHELAKAKIS H. (2005) ELEVATED PLASMA CHEMOKINE CCL18/PARC IN β-THALASSEMIA. BLOOD CELLS, MOLECULES, & DISEASES. 35, 328-331.
  20. DOULGERAKI A., ATHANASOPOULOU H., VOSKAKI I., TZAGARAKI A., KARABATSOS F., FRAGODIMITRI C., GEORGAKOPOULOU E., IOUSEF J., MONOPOLIS I., CHATZILIAMI A., and KARAGIORGA M. (2012) BONE HEALTH EVALUATION OF CHILDREN AND ADOLESCENTS WITH HOMOZYGOUS β-THALASSEMIA: IMPLICATIONS FOR PRACTICE. J PEDIATR HEMATOL ONCOL. 34(5), 344-348.
  21. FELDHAMMER M., DURAND S., MRAZOVA L., BOUCHER R.-M., LAFRAMBOISE R., STEINFELD R., WRAITH J., MICHELAKAKIS H., VAN DIGGELEN O., HREBICEK M., KMOCH S., and PSHEZHETSKY A. (2009) SANFILIPPO SYNDROME TYPE C: MUTATION SPECTRUM IN THE HEPARAN SULFATE ACETYL-CoA: α-GLUCOSAMINIDE N-ACETYLTRANSFERASE (HGSNAT) GENE. HUMAN MUTATION. 30(6), 918-925.
  22. FOTOULAKI M., SCHUCHMAN E.H., SIMONARO C.M., AUGOUSTIDES-SAVVOPOULOU P., MICHELAKAKIS H., PANAGOPOULOU P., VARLAMIS G., and NOUSIA-ARVANITAKIS S. (2007) ACID SPHINGOMYELINASE-DEFICIENT NIEMANN-PICK DISEASE: NOVEL FINDINGS IN A GREEK CHILD. J INHERIT METAB DIS. 30(6), 986.
  23. GEORGALA S., PAPASSOTIRIOU I., GEORGALA C., DEMETRIOU E., and SCHULPIS K. (2005) ISOTRETINOIN THERAPY INDUCES DNA OXIDATIVE DAMAGE. CLIN CHEM LAB MED. 43(11), 1178-1182.
  24. GIBICAR D., HORVAT M., NAKOU S., SARAFIDOU J., and YAGER J. (2006) PILOT STUDY OF INTRAUTERINE EXPOSURE TO METHYLMERCURY IN EASTERN AEGEAN ISLANDS, GREECE. SCIENCE OF THE TOTAL ENVIRONMENT. 367, 586-595.
  25. GUIPPONI M., TOH M.-Y., TAN J., PARK D., HANSON K., BALLANA E., KWONG D., CANNON P.Z.F., WU Q., GOUT A., DELORENZI M., SPEED T., SMITH R.J.H., DAHL H.H., PETERSEN M., TEASDALE R.D., ESTIVILL X., PARK W.-J., and SCOTT H.S. (2008) AN INTEGRATED GENETIC AND FUNCTIONAL ANALYSIS OF THE ROLE OF TYPE II TRANSMEMBRANE SERINE PROTEASES (TMPRSSs) IN HEARING LOSS.HUMAN MUTATION. 29(1), 130-141.
  26. HERON B., MIKAELOFF Y., FROISSART R., CARIDADE G., MAIRE I., CAILLAUD C., LEVADE T., CHABROL B., FEILLET F., OGIER H., VALAYANNOPOULOS V., MICHELAKAKIS H., ZAFEIRIOU D., LAVERY L., WRAITH E., DANOS O., HEARD J.-M., and TARDIEU M. (2011) INCIDENCE AND NATURAL HISTORY OF MUCOPOLYSACCHARIDOSIS TYPE III IN FRANCE AND COMPARISON WITH UNITED KINGDOM AND GREECE. AMERICAN JOURNAL OF MEDICAL GENETICS. PART A, 58-68.
  27. HEWITT A., SAMPLES J., ALLINGHAM R., JARVELA I., KITSOS G., KRISHNADAS S., RICHARDS J., LICHTER P., PETERSEN M., SUNDARESAN P., WIGGS J., MACKEY D., and WIRTZ M. (2007) INVESTIGATION OF FOUNDER EFFECTS FOR THE THR377MET MYOCILIN MUTATION IN GLAUCOMA FAMILIES FROM DIFFERING ETHNIC BACKGROUNDS. MOLECULAR VISION. 13, 487-492.
  28. HILGERT N., ALASTI F., DIELTJENS N., PAWLIK B., WOLLNIK B., UYGUNER O., DELMAGHANI S., WEIL D., PETIT C., DANIS E., YANG T., PANDELIA E., PETERSEN M.B., GOOSSENS D., FAVERO J.D., SANATI M.H., SMITH R.J., and VAN VAMP G. (2008) MUTATION ANALYSIS OF TMC1 IDENTIFIES FOUR NEW MUTATIONS AND SUGGESTS AN ADDITIONAL DEAFNESS GENE AT LOCI DFNA36 AND DFNB7/11. CLIN GENET. 74, 223-232.
  29. HILGERT N., HUENTELMAN M.J., THORBURN A.Q., FRANSEN E., DIELTJENS N., MUELLER-MALESINSKA M., POLLAK A., SKORKA A., WALIGORA J., PLOSKI R., CASTORINA P., PRIMIGNANI P., AMBROSETTI U., MURGIA A., ORZAN E., PANDYA A., ARNOS K., NORRIS V., SEEMAN P., JANOUSEK P., FELDMANN D., MARLIN S., DENOYELLE F., NISHIMURA C.J., JANECKE A., NEKAHM-HEIS D., MARTINI A., MENNUCCI E., TOTH T., SZIKLAI I., DEL CASTILLO I., MORENO F., PETERSEN M.B., ILIADOU V., TEKIN M., INCESULU A., NOWAKOWSKA E., BAL J., VAN DE HEYNING P., ROUX A.-F., BLANCHET C., GOIZET C., LANCELOT G., FIALHO G., CARIA H., ZHONG LIU X., XIAOMEI O., GOVAERTS P., GRONSKOV K., HOSTMARK K., FREI K., DHOOGE I., VLAEMINCK S., KUNSTMANN E., VAN LAER L., SMITH R.J.H., and VAN CAMP G. (2009) PHENOTYPIC VARIABILITY OF PATIENTS HOMOZYGOUS FOR THE GJB2 MUTATION 35DELG CANNOT BE EXPLAINED BY THE INFLUENCE OF ONE MAJOR MODIFIER GENE. EUROPEAN JOURNAL OF HUMAN GENETICS. 17, 517-524.
  30. HOFER D., PAUL K., FANTUR K., BECK M., BURGER F., CAILLAUD C., FUMIC K., LADVINOVA J., LUGOWSKA A., MICHELAKAKIS H., RADEVA B., RAMASWAMI U., PLECKO B., and PASCHKE E. (2009) GM1 GANGLIOSIDOSIS AND MORQUIO B DISEASE: EXPRESSION ANALYSIS OF MISSENSE MUTATIONS AFFECTING THE CATALYTIC SITE OF ACID β-GALACTOSIDASE. HUMAN MUTATION. 30(8), 1214-1221.
  31. HOFER D., PAUL K., FANTUR K., BECK M., ROUBERGE A., VELLODI A., POORTHUIS B.J., MICHELAKAKIS H., PLECKO B., and PASCHKE E. (2010) PHENOTYPE DETERMINING ALLELES IN GM1 GANGLIOSIDOSIS PATIENTS BEARING NOVEL GLB1 MUTATIONS. CLINICAL GENETICS. 78(3), 236-246. 
  32. HOLLAK C., AERTS J., BELMATOUG N., BEMBI B., BODAMER O., CAPPELLINI D., COLLIN-HISTED T., COX T., DEEGAN P., GIRALDO P., HUGHES D., LUKINA E., MANUEL J., MICHELAKAKIS H., DI ROCCO M., VELLODI A., and ZIMRAN A. (2010) GUIDELINES FOR THE RESTART OF IMIGLUCERASE IN PATIENTS WITH GAUCHER DISEASE: RECOMMENDATIONS FROM THE EUROPEAN WORKING GROUP ON GAUCHER DISEASE. BLOOD CELLS MOL DIS. 44(2), 86-87.
  33. HOLLAK C., VOM DAHL S., AERTS J., BELMATOUG N., BEMBI B., COHEN Y., COLLIN H., DEEGAN P., VAN DUSSEN L., GIRALDO P., MENGEL E., MICHELAKAKIS H., MANUEL J., HREBICEK M., PARINI R., REINKE J., DI ROCCO M., POCOVI M., SA MIRANDA M., TYLKI-SZYMANSΚA A., ZIMRAU A., and COX T. (2009) FORCE MAJEURE: THERAPEUTIC MEASURES IN RESPONSE TO RESTRICTED SUPPLY OF IMIGLUCERASE (CEREZYME) FOR PATIENTS WITH GAUCHER DISEASE. BLOOD CELLS MOL DIS. 1544(1), 41-47.
  34. HOLLAK C., VOM DAHL S., AERTS J., BELMATOUG N., BEMBI B., COHEN Y., COLLIN-HISTED T., DEEGAN P., VAN DUSSEN L., GIRALDO P., MENGEL E., MICHELAKAKIS H., MANUEL J., HREBICEK M., PARINI R., REINKE J., DI ROCCO M., POCOVI M., SA MIRANDA M., TYLKI-SZYMANSKA A., ZIMRAN A., and COX T. (2010) FORCE MAJEURE: THERAPEUTIC MEASURES IN RESPONSE TO RESTRICTED SUPPLY OF IMIGLUCERASE (CEREZYME) FOR PATIENTS WITH GAUCHER DISEASE. BLOOD CELLS MOL DIS. 44(1), 41-47.
  35. ILIADOU V., VAN DEN BOGAERT K., ELEFTHERIADES N., APERIS G., VANDERSTRAETEN K., FRANSEN E., THYS M., GRIGORIADOU M., PAMPANOS A., ECONOMIDES J., ILIADES T., VAN CAMP G., and PETERSEN M. (2006) MONOGENIC NONSYNDROMIC OTOSCLEROSIS: AUDIOLOGICAL AND LINKAGE ANALYSIS IN A LARGE GREEK PEDIGREE. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY. 70, 631-637.
  36. KALOUMENOU I., ALEVIZAKI M., LADOPOULOS C., ANTONIOU A., DUNTAS L., MASTORAKOS G., CHIOTIS D., MENGRELI C., LIVADAS S., XEKOUKI P., and DACOU-VOUTETAKIS C. (2007) THYROID VOLUME AND ECHOSTRUCTURE IN SCHOOLCHILDREN LIVING IN AN LODINE-REPLETE AREA: RELATION TO AGE, PUBERTAL STAGE, AND BODY MASS INDEX. THYROID. 17(9), 875-881.
  37. KALOUMENOU I., DUNTAS L., ALEVIZAKI M., MANTZOU E., CHIOTIS D., MENGRELI C., PAPASSOTIRIOU I., MASTORAKOS G., and DACOU-VOUTETAKIS C. (2010) GENDRER, AGE, PUBERTY, AND BMI RELATED CHANGES OF TSH AND THYROID HORMONES IN SCHOOLCHILDREN LIVING IN A LONG-STANDING IODINE REPLETE AREA. HORM METAB RES. 42(4), 285-289.
  38. KARADIMAS C., SIFAKIS S., VALSAMOPOULOS P., MAKATSORIS C., VELISSARIOU V., NASIOULAS G., PETERSEN M.B., KOUMANTAKIS E., and HATZAKI A. (2006) CLINICAL REPORT PRENATAL DIAGNOSIS OF HYPOCHONDROPLASIA: REPORT OF TWO CASES. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 140A, 998-1003.
  39. KARADIMAS C., TROUVAS D., HARITATOS G., MAKATSORIS C., DEDOULIS E., VELISSARIOU V., ANTONIADI T., HATZAKI A., and PETERSEN M. (2006) PRENATAL DIAGNOSIS OF ACHONDROPLASIA PRESENTING WITH MULTIPLE-SUTURE SYNOSTOSIS: A NOVEL ASSOCIATION. PRENATAL DIAGNOSIS. 26, 258-261.
  40. KARIKAS G., KRIEBARDIS A., SAMARA I., SCHULPIS I., PAPACHRISTODOULOU M., and FYTOU-PALLIKARI A. (2006) SERUM HOMOCYSTEINE LEVELS AND PARAOXONASE 1 ACTIVITY IN PRESCHOOL AGED CHILDREN IN GREECE. CLIN CHEM LAB MED. 44(5), 623-627.
  41. KARIKAS G., SCHULPIS K., BARTZELIOTOU A., KARAKONSTANTAKIS T., GEORGALA S., KANAVAKI I., DEMETRIOU E., and PAPASSOTIRIOU I. (2006) LIPIDS, LIPOPROTEINS, APOLIPOPROTEINS, SELECTED TRACE ELEMENTS AND MINERALS IN THE SERUM OF CHILDREN ON VALPROIC ACID MONOTHERAPY. PHARMACOLOGY & TOXICOLOGY. 98, 599-603.
  42. KARIKAS G., SCHULPIS K., BARTZELIOTOU A., REGOUTAS S., THANOPOULOU C., PAPAEVANGELOU V., GIANNOULIA-KARANTANA A., PAPASSOTIRIOU I., and FYTOU-PALLIKARI A. (2009) EARLY EFFECTS OF SODIUM VALPROATE MONOTHERAPY ON SERUM PAPAOXONASE/ARYLESTERASE ACTIVITIES. THE SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION. 69(1), 31-35.
  43. KHAKOO G., SOFIANOU-KATSOULIS A., PERKIN M., and LACK G. (2008) CLINICAL FEATURES AND NATURAL HISTORY OF PHYSICAL URTICARIA IN CHILDREN. PEDIATR ALLERGY IMMUNOL. 19, 363-366.
  44. KITSOS G., PETROU Z., GRIGORIADOU M., SAMPLES J., HEWITT A., KOKOTAS H., GIANNOULIA-KARANTANA A., MACKEY D., WIRTZ M., MOSCHOU M., IOANNIDIS J., and PETERSEN M. (2010) PRIMARY OPEN ANGLE GLAUCOMA DUE TO T377M MYOC: POPULATION MAPPING OF A GREEK FOUNDER MUTATION IN NORTHWESTERN GREECE. CLINICAL OPHTHALMOLOGY. 4, 171-178.
  45. KOKOTAS H. and PETERSEN M.B. (2010) CLINICAL AND MOLECULAR ASPECTS OF ANIRIDIA. CLINICAL GENETICS. 77, 409-420.
  46. KOKOTAS H., GRIGORIADOU M., and PETERSEN M. (2011) AGE-RELATED MACULAR DEGENERATION: GENETIC AND CLINICAL FINDINGS. CLIN CHEM LAB MED. 49(4).
  47. KOKOTAS H., GRIGORIADOU M., HATZAKI A., ANTONIADI T., GIANNOULIA-KARANTANA A., and PETERSEN M.B. (2010) EASY, RAPID, AND COST-EFFECTIVE METHODS FOR IDENTIFYING CARRIERS OF RECURRENT GJB2 MUTATIONS CAUSING NONSYNDROMIC HEARING IMPAIRMENT IN THE GREEK POPULATION. GENETIC TESTING AND MOLECULAR BIOMARKERS. 14(2), 189-192.
  48. KOKOTAS H., GRIGORIADOU M., KORRES G., FEREKIDOU E., GIANNOULIA-KARANTANA A., KANDILOROS D., KORRES S., and PETERSEN M. (2010) ARE GJB2 MUTATIONS AN AGGRAVATING FACTOR IN THE PHENOTYPIC EXPRESSION OF MITOCHONDRIAL NON-SYNDROMIC DEAFNESS?JOURNAL OF HUMAN GENETICS. 55, 265-269.
  49. KOKOTAS H., GRIGORIADOU M., KORRES G., FEREKIDOU E., KANDILOROS D., KORRES S., and PETERSEN M. (2010) SCREENING OF A GREEK DEAFNESS POPULATION FOR THE A7445G MITOCHONDRIAL DNA MUTATION. MOLECULAR GENETICS AND METABOLISM. 100, 300-301.
  50. KOKOTAS H., GRIGORIADOU M., KORRES G., FEREKIDOU E., PAPADOPOULOU E., NEOU P., GIANNOULIA-KARANTANA A., KANDILOROS D., KORRES S., and PETERSEN M. (2009) THE A1555G MITOCHONDRIAL DNA MUTATION IN GREEK PATIENTS WITH NON-SYNDROMIC, SENSORINEURAL HEARING LOSS. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. 390, 755-757.
  51. KOKOTAS H., GRIGORIADOU M., MIKKELSEN M., GIANNOULIA-KARANTANA A., and PETERSEN M. (2009) INVESTIGATING THE IMPACT OF THE DOWN SYNDROME RELATED COMMON MTHFR 677C>T POLYMORPHISM IN THE DANISH POPULATION. DISEASE MARKERS. 27, 279-285.
  52. KOKOTAS H., GRIGORIADOU M., YANG L., LODAHL M., DAHL RENDTORFF N., GYFTODIMOU Y., KORRES G., FEREKIDOU E., KANDILOROS D., KORRES S., TRANEBJAERG L., GUAN M.-X., and PETERSEN M.B. (2011) HOMOPLASMY OF THE G7444A mtDNA AND HETEROZYGOSITY OF THE GJB2 c.35delG MUTATIONS IN A FAMILY WITH HEARING LOSS. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY. 75, 89-94.
  53. KOKOTAS H., PETERSEN M.B., and WILLEMS P.J. (2007) MITOCHONDRIAL DEAFNESS. CLINICAL GENETICS. 71, 379-391.
  54. KOKOTAS H., THEODOSIOU M., KORRES G., GRIGORIADOU M., FEREKIDOU E., GIANNOULIA-KARANTANA A., PETERSEN M.B., and KORRES S. (2008) SUDDEN HEARING LOSS IN A FAMILY WITH GJB2 RELATED PROGRESSIVE DEAFNESS.INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY. 72, 1735-1740.
  55. KOKOTAS H., VAN LAER L., GRIGORIADOU M., ILIADOU V., ECONOMIDES J., POMONI S., PAMPANOS A., ELEFTHERIADES N., FEREKIDOU E., KORRES S., GIANNOULIA-KARANTANA A., VAN CAMP G., and PETERSEN M.B. (2008) STRONG LINKAGE DISEQUILIBRIUM FOR THE FREQUENT GJB2 35delG MUTATION IN THE GREEK POPULATION. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 146A, 2879-2884.
  56. KOLAITIS G., PAPANIKOLAOU K., PALIOKOSTA E., TSIANTIS J., GYFTODIMOU Y., SARRI C., PETERSEN M.B., and KOKOTAS H. (2009) DE NOVO INVERTED INTERSTITIAL DUPLICATION 8q22.1 - q21.1 IN A BOY WITH MODERATE LEARNING DISABILITIES, MILD AUTISTIC AND DYSMORPHIC FEATURES. ADVANCES IN MENTAL HEALTH AND LEARNING DISABILITIES. 3(2), 48-52.
  57. KONSTANTINIDOU A., AGROGIANNIS G., SIFAKIS S., KARANTANAS A., HARAKOGLOU V., KAMINOPETROS P., HATZAKI A., PETERSEN M., KARADIMAS C., VELISSARIOU V., VELONIS S., PAPANTONIOU N., ANTSAKLIS A., and PATSOURIS E. (2009) GENETIC SKELETAL DISORDERS OF THE FETUS AND INFANT: PATHOLOGIC AND MOLECULAR FINDINGS IN A SERIES OF 41 CASES. BIRTH DEFECTS RESEARCH (PART A): CLINICAL AND MOLECULAR TERATOLOGY. 85, 811-821.
  58. KONSTANTINIDOU A., ANNINOS H., GYFTODIMOU Y., PETERSEN M., KARADIMAS C., FOTOPOULOS S., PARASKEVAKOU H., AKMAN H., DIMAURO S., and PATSOURIS E. (2006) NEONATAL NEUROMUSCULAR VARIANT OF GLYCOGEN STORAGE DISEASE TYPE IV: HISTOPATHOLOGICAL FINDINGS LEADING TO THE DIAGNOSIS.HISTOPATHOLOGY. 48, 878-880.
  59. KONSTANTINIDOU A., KARADIMAS C., WATERHAM H.R., SUPERTI-FURGA A., KAMINOPETROS P., GRIGORIADOU M., KOKOTAS H., AGROGIANNIS G., GIANNOULIA-KARANTANA A., PATSOURIS E., and PETERSEN M.B. (2008) PATHOLOGIC, RADIOGRAPHIC AND MOLECULAR FINDINGS IN THREE FETUSES DIAGNOSED WITH HEM/GREENBERG SKELETAL DYSPLASIA. PRENATAL DIAGNOSIS. 28, 309-312.
  60. KONSTANTINIDOU A.E., ANNINOS H., DERTINGER S., NONNI A., PETERSEN M., KARADIMAS C., HAVAKI S., MARINOS E., AKMAN H.O., DiMAURO S., and PATSOURIS E. (2008) PLACENTAL INVOLVEMENT IN GLYCOGEN STORAGE DISEASE TYPE IV. PLACENTA. 29, 378-381.
  61. KOROMILAS C., LIAPI C., SCHULPIS K., KALAFATAKIS K., ZARROS A., and TSAKIRIS S. (2010) STRUCTURAL AND FUNCTIONAL ALTERATIONS IN THE HIPPOCAMPUS DUE TO HYPOTHYROIDISM. METAB BRAIN DIS. 25, 339-354.
  62. KROOS M., MANTA P., MAVRIDOU I., MUNTONI F., HALLEY D., VAN DER HELM R., ZAIFEIRIOU D., VAN DER PLOEG A., REUSER A., and MICHELAKAKIS H. (2006) SEVEN CASES OF POMPE DISEASE FROM GREECE. J INHERIT METAB DIS. 29, 556-563.
  63. KROOS M., POMPONIO R., VAN VLIET L., PALMER R., PHIPPS M., VAN DER HELM R., HALLEY D., REUSER A., and THE GAA DATABASE CONSORTIUM (MAVRIDOU I. and MICHELAKAKIS H.) (2008) UPDATE OF THE POMPE DISEASE MUTATION DATABASE WITH 107 SEQUENCE VARIANTS AND A FORMAT FOR SEVERITY RATING. HUMAN MUTATION. 29(6), E13-E26.
  64. KROOS M., HOOGEVEEN-WESTERVELD M., MICHELAKAKIS H., POMPONIO R., VAN DER PLOEG A., HALLEY D., REUSER A., and GAA DATABASE CONSORTIUM. (2012) UPDATE OF THE POMPE DISEASE MUTATION DATABASE WITH 60 NOVEL GAA SEQUENCE VARIANTS AND ADDITIONAL STUDIES ON THE FUNCTIONAL EFFECT OF 34 PREVIOUSLY REPORTED VARIANTS. HUMAN MUTATION. 33(8), 1161-1165.
  65. LABADARIDIS I., DIMITRIOU E., THEODORAKIS M., KAFALIDIS G., VELEGRAKI A., and MICHELAKAKIS H. (2005) CHITOTRIOSIDASE IN NEONATES WITH FUNGAL AND BACTERIAL INFECTIONS. ARCH DIS CHILD FETAL NEONATAL ED.90, F531-F532.
  66. LABADARIDIS I., MORAITOU M., THEODORAKI M., DIMITRIOU E., SARAFIDOU J., and MICHELAKAKIS H. (2007) LINOLEIC AND ARACHIDONIC ACID IN PERINATAL ASPHYXIA AND PREMATURITY. THE JOURNAL OF MATERNAL-FETAL AND NEONATAL MEDICINE. 20(8), 623-626.
  67. LABADARIDIS I., MORAITOU M., THEODORAKI M., TRIANTAFYLLIDIS G., SARAFIDOU J., and MICHELAKAKIS H. (2009) PLASMALOGEN LEVELS IN FULL-TERM NEONATES. ACTA PAEDIATRICA. 98, 640-642.
  68. LIANOU D., GALLEGO L., MICHELAKAKIS H., PEREZ-CERDA C., PEREZ B., GINIS S., JAKOBS C., UGARTE M., and DESVIAT L. (2010) FUNCTIONAL ANALYSIS OF A NOVEL MUTATION IN THE PCCA GENE IDENTIFIED IN A LATE-INFANTILE ONSET PROPIONIC ACIDEMIA PATIENT. CLIN CHIM ACTA. 411(17-18), 1388-1389.
  69. LIAPPAS I., TZAVELLAS E., KARIYANNIS C., PIPERI C., SCHULPIS K., PAPASSOTIRIOU I., and SOLDATOS C. (2006) EFFECT OF ALCOHOL DETOXIFICATION ON SERUM S-100B LEVELS OF ALCOHOL-DEPENDENT INDIVIDUALS. IN VIVO. 20, 675-680.
  70. LIVADAS S., MAGIAKOU M.-A., MENGRELI C., GIRGINOUDIS P., GALANI C., SMYRNAKI P., KANAKA-GANTENBEIN C., XEKOUKI P., CHROUSOS G., and DACOU-VOUTETAKIS C. (2007) OBESITY AND ATTENUATED ADIPOSITY REBOUND IN CHILDREN WITH CONGENITAL HYPOTHYROIDISM. NORMALIZATION OF BMI VALUES IN ADOLESCENTS. HORM METAB RES. 39, 524-528.
  71. LOUIZOU E., MICHELAKAKIS H., KOMIANOU F., Di PERNA M., BISCEGLIA I., and DEDOUSIS G. (2007) HUMAN GENE MUTATIONS. GENE SYMBOL: SLC7Aq. DISEASE: CYSTINURIA. HUM GENET. 122(2), 214.
  72. LUGOWSKA A., AMARAL O., BERGER J., BERNA L., BOSSHARD N., CHABAS A., FENSOM A., GIESELMANN V., GOROVENKO G., LISSENS W., MANSSON J.-E., MARCAO A., MICHELAKAKIS H., BERNHEIMER H., OL'KHOVYCH N., REGIS S., SINKE R., TYLKI-SZYMANSKA A., and CZARTORYSKA B. (2005) MUTATIONS c.459 + 1G>A AND p.P426L IN THE ARSA GENE: PREVALENCE IN METACHROMATIC LEUKODYSTROPHY PATIENTS FROM EUROPEAN COUNTRIES. MOLECULAR GENETICS AND METABOLISM. 86, 353-359.
  73. MACHATKOVA M., BROUCKOVA M., MATEJCKOVA M., KREBSOVA A., SPERLING K., VORSANOVA S., KUTSEV S., ZEROVA T., ARBUZOVA S., KREJCI R., PETERSEN M., and MACEK M. (2005) QF-PCR EXAMINATION OF PARENTAL AND MEIOTIC ORIGIN OF TRISOMY 21 IN CENTRAL AND EASTERN EUROPE. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY. 53(3), 371-373.
  74. MAJAVA M., HOORNAERT K., BATHHOLDI D., BOUMA M., BOUMAN K., CARRERA M., DEVRIENDT K., HURST J., KITSOS G., NIEDRIST D., PETERSEN M., SHEARS D., STOLTE-DIJKSTRA I., VAN HAGEN J., ALA-KOKKO L., MANNIKKO M., and MORTIER G. (2007) A REPORT ON 10 NEW PATIENTS WITH HETEROZYGOUS MUTATIONS IN THE COL11A1 GENE AND A REVIEW OF GENOTYPE-PHENOTYPE CORRELATIONS IN TYPE XI COLLAGENOPATHIES. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 143A, 258-264.
  75. MANOLAKOS E., KEFALAS K., NEROUTSOU R., LAGOU M., KOSYAKOVA N., EWERS E., ZIEGLER M., WEISE A., TSOPLOU P., RAPTI S.-M., PAPOULIDIS I., ANASTASAKIS E., GARAS A., SOTIRIOU S., ELEFTHERIADES M., PEITSIDIS P., MALATHRAKIS D., THOMAIDIS L., KITSOS G., ORRU S., LIEHR T., PETERSEN M., and KITSIOU-TZELI S. (2010) CHARACTERIZATION OF 23 SMALL SUPERNUMERARY MARKER CHROMOSOMES DETECTED AT PRE-NATAL DIAGNOSIS: THE VALUE OF FLUORESCENCE IN SITU HYBRIDIZATION. MOLECULAR MEDICINE REPORTS. 3, 1015-1022.
  76. MANOLAKOS E., KOSYAKOVA N., THOMAIDIS L., NEROUTSOU R., WEISE A., MIHALATOS M., ORRU S., KOKOTAS H., KITSOS G., LIEHR T., and PETERSEN M.B. (2008) COMPLEX CHROMOSOME REARRANGEMENT IN A CHILD WITH MICROCEPHALY, DYSMORPHIC FACIAL FEATURES AND MOSAICISM FOR A TERMINAL DELETION DEL (18) (q21.32-qter) INVESTIGATED BY FISH AND ARRAY-CGH: CASE REPORT. MOLECULAR CYTOGENETICS. 11 1(1), 24.
  77. MANOLAKOS E., ORRU S., NEROUTSOU R., KEFALAS K., LOUIZOU E., PAPOULIDIS I., THOMAIDIS L., PEITSIDIS P., SOTIRIOU S., KITSOS G., TSOPLOU P., PETERSEN M., and METAXOTOU A. (2009) DETAILED MOLECULAR AND CLINICAL INVESTIGATION OF A CHILD WITH A PARTIAL DELETION OF CHROMOSOME 11 (JACOBSEN SYNDROME). MOLECULAR CYTOGENETICS. 2, 26.
  78. MANOLAKOS E., PEITSIDIS P., ELEFTHERIADES M., DEDOULIS E., ZIEGLER M., ORRU S., LIEHR T., and PETERSEN M. (2010) PRENATAL DETECTION OF FULL MONOSOMY 21 IN A FETUS WITH INCREASED NUCHAL TRANSLUCENCY: MOLECULAR CYTOGENETIC ANALYSIS AND REVIEW OF THE LITERATURE. THE JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH. 36 (2), 435-440.
  79. MANOLAKOS E., VETRO A., KEFALAS K., RAPTI S.-M., LOUIZOU E., GARAS A., KITSOS G., VASILEIADIS L., TSOPLOU P., ELEFTHERIADES M., PEITSIDIS P., ORRU S., LIEHR T., PETERSEN M., and THOMAIDIS L. (2010) THE USE OF ARRAY-CGH IN A COHORT OF GREEK CHILDREN WITH DEVELOPMENTAL DELAY. MOLECULAR CYTOGENETICS. 3, 22.
  80. MANOLAKOS E., VETRO A., KITMIRIDES S., PAPOULIDIS I., KOSYAKOVA N., MRASEK K., WEISE A., AGAPITOS E., ORRU S., PEITSIDIS P., LIEHR T., and PETERSEN M.B. (2009) PRENATAL DIAGNOSIS OF A FETUS WITH RING CHROMOSOME 15 CHARACTERIZED BY ARRAY-CGH. PRENATAL DIAGNOSIS. 29, 884-888.
  81. MARINOU K., TSAKIRIS S., TSOPANAKIS C., SCHULPIS K., and BEHRAKIS P. (2005) Mg2+ -ATPase ACTIVITY IN SUCKLING RAT BRAIN REGIONS IN GALACTOSAEMIA IN VITRO. L-CYSTEINE AND GLUTATHIONE EFFECTS. TOXICOLOGY IN VITRO. 19, 167-172.
  82. MARINOU K., TSAKIRIS S., TSOPANAKIS C., SCHULPIS K., and BEHRAKIS P. (2005) SUCKLING RAT BRAIN REGIONAL DISTRIBUTION OF ACETYLCHOLINESTERASE ACTIVITY IN GALACTOSAEMIA IN VITRO. METABOLIC BRAIN DISEASE. 20(3), 227-236.
  83. MARINOU K., TSAKIRIS S., TSOPANAKIS C., SCHULPIS K., and BEHRAKIS P. (2005) SUCKLING RAT BRAIN REGIONAL DISTRIBUTION OF NA+, K+ -ATPase ACTIVITY IN THE IN VITRO GALACTOSAEMIA: THE EFFECT OF L-CYSTEINE AND GLUTATHIONE. METABOLIC BRAIN DISEASE. 20(1), 45-54.
  84. MARGONI D., CHOULIARAS G., DUSCAS G., VOSKAKI I., VOUTSAS N., PAPADOPOULOU A., PANAYIOTOU J., and ROMA E. (2012) BONE HEALTH IN CHILDREN WITH CELIAC DISEASE ASSESSED BY DUAL X-RAY ABSORPTIOMETRY: EFFECT OF GLUTEN-FREE DIET AND PREDICTIVE VALUE OF SERUM BIOCHEMICAL INDICES. J PEDIATR GASTROENTEROL NUTR. 54(5), 680-4.
  85. MENGRELI C., KANAKA-GANTENBEIN C., GIRGINOUDIS P., MAGIAKOU M.-A., CHRISTAKOPOULOU I., GIANNOULIA-KARANTANA A., CHROUSOS G., and DACOU-VOUTETAKIS C. (2010) SCREENING FOR CONGENITAL HYPOTHYROIDISM: THE SIGNIFICANCE OF THRESHOLD LIMIT IN FALSE-NEGATIVE RESULTS. JCEM: THE JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 95(9), 4283-4290.
  86. MICHELAKAKIS H., DIMITRIOU E., MORAITOU M., VALARI M., MITSIADI V., YATRAKOU E., KARACHRISTOU K., COZAR M., VILAGELIU L., and GRINBERG D. (2010) PERINATAL LETHAL FORM OF GAUCHER DISEASE. CLINICAL AND MOLECULAR CHARACTERIZATION OF A GREEK CASE. BLOOD CELLS, MOLECULES, AND DISEASES. 44, 82-83.
  87. MICHELAKAKIS H., KARIYANNIS C., MORAITOU M., DIMITRIOU E., SARAFIDOU J., and PAPASSOTIRIOU I. (2007) SERUM S100B LEVELS IN X-LINKED ADRENOLEUKODYSTROPHY AND GAUCHER DISEASE. JIMD.
  88. MICHELAKAKIS H., MORAITOU M., DIMITRIOU E., SANTAMARIA R., SANCHEZ G., GORT L., CHABAS A., GRINBERG D., DASSOPOULOU M., FOTOPOULOS S., and VILAGELIU L. (2006) HOMOZYGOSITY FOR THE DOUBLE D409H + H255Q ALLELE IN TYPE II GAUCHER DISEASE. JIMD. 11.
  89. MICHELAKAKIS H., MORAITOU M., MAVRIDOU I., and DIMITRIOU E. (2009) PLASMA LYSOSOMAL ENZYME ACTIVITIES IN CONGENITAL DISORDERS OF GLYCOSYLATION, GALACTOSEMIA AND FRUCTOSEMIA. CLINICA CHIMICA ACTA. 401, 81-83.
  90. MICHELAKAKIS H., XIROMERISIOU G., DARDIOTIS E., BOZI M., VASSILATIS D., KOUNTRA P.-M., PATRAMANI G., MORAITOU M., PAPADIMITRIOU D., STAMBOULIS E., STEFANIS L., ZINTZARAS E., and HADJIGEORGIOU G. (2012) EVIDENCE OF AN ASSOCIATION BETWEEN THE SCAVENGER RECEPTOR CLASS B MEMBER 2 GENE AND PARKINSON'S DISEASE. MOVEMENT DISORDERS.
  91. MORAITOU M., DIMITRIOU E., ZAFEIRIOU D., REPPA C., MARINAKIS T., SARAFIDOU J., and MICHELAKAKIS H. (2008) PLASMALOGEN LEVELS IN GAUCHER DISEASE. BLOOD CELLS, MOLECULES, AND DISEASES. 41(2), 196-199.
  92. MORAITOU M., DIMITRIOU E., MAVRIDOU I., MICHELAKAKIS H., GEORGOULI H., PLOSKI R., and POLLAK A. (2012) TRANSFERRIN ISOELECTRIC FOCUSING AND PLASMA LYSOSOMAL ENZYME ACTIVITIES IN THE DIAGNOSIS AND FOLLOW-UP OF HEREDITARY FRUCTOSE INTOLERANCE. CLINICA CHIMICA ACTA. 413(19-20), 1714-1715.
  93. NARANJO S., VOESENEK K., DE LA CALLE-MUSTIENES E., ROBERT-MORENO A., KOKOTAS H., GRIGORIADOU M., ECONOMIDES J., VAN CAMP G., HILGERT N., MORENO F., ALSINA B., PETERSEN M., KREMER H., and GOMEZ-SKARMETA J. L. (2010) MULTIPLE ENHANCERS LOCATED IN A 1-Mb REGION UPSTREAM OF POU3F4 PROMOTE EXRESSION DURING INNER EAR DEVELOPMENT AND MAY BE REQUIRED FOR HEARING. HUM GENET. 128, 411-419.
  94. NIKOLAIDIS G. (2010) "FROM PASSIONS" TO "EMOTIONS" AND VISA VERSA: HISTORICAL TRANSFORMATIONS OF THE THEORETICAL CONCEPT OF EMOTIONS AND RESPECTFUL CLINICAL IMPLICATIONS. ASKLEPIOS: INTERNATIONAL ANNUAL OF HISTORY AND PHILOSOPHY OF THE MEDICINE. IV, 58-66.
  95. NTINAPOGIAS A. (2009) RISK FACTORS FOR INJURIES AMONG ELDERLY MALES AND MALE GENDER AS "RISK FACTOR". THE AGING MALE. 12, 4.
  96. PAPADIMAS G., SPENGOS K., KONSTANTINOPOULOU A., VASSILOPOULOU S., VONTZALIDIS A., PAPADOPOULOS C., MICHELAKAKIS H., and MANTA P. (2011) ADULT POMPE DISEASE: CLINICAL MANIFESTATIONS AND OUTCOME OF THE FIRST GREEK PATIENTS RECEIVING ENZYME REPLACEMENT THERAPY. CLINICAL NEUROLOGY AND NEUROSURGERY. EPUB AHEAD OF PRINT.
  97. PAPADIMAS G., TERZIS G., METHENITIS S., SPENGOS K., PAPADOPOULOS C., VASSILOPOULOU S., KAVOURAS S., MICHELAKAKIS H., and MANTA P. (2011) BODY COMPOSITION ANALYSIS IN LATE-ONSET POMPE DISEASE. MOLECULAR GENETICS AND METABOLISM. 102(1), 41-43.
  98. PAPADOPOULOU E., SIFAKIS S., ROGALIDOU M., MAKRIGIANNAKIS A., GIANNAKOPOULOU C., and PETERSEN M. (2005) 3C SYNDROME WITH CRYPTORCHIDISM AND POSTERIOR EMBRYOTOXON. CLINICAL DYSMORPHOLOGY. 14, 97-100.
  99. PAPADOPOULOU E., SIFAKIS S., SARRI C., GYFTODIMOU J., LIEHR T., MRASEK K., KALMANTI M., and PETERSEN M. (2006) A REPORT OF PURE 7p DUPLICATION SYNDROME AND REVIEW OF THE LITERATURE. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 140A, 2802-2806.
  100. PAPAEFTHYMIOU H., KRITIDIS P., ANOUSIS J., and SARAFIDOU J. (2005) COMPARATIVE ASSESSMENT OF NATURAL RADIOACTIVITY IN FALLOUT SAMPLES FROM PATRAS AND MEGALOPOLIS, GREECE. JOURNAL OF ENVIRONMENTAL RADIOACTIVITY.
  101. PAPOUTSAKIS C., MANIOS Y., MAGKOS F., PAPACONSTANTINOU E., SCHULPIS K., ZAMPELAS A., MATALAS A., and YIANNAKOURIS N. (2010) EFFECT OF THE METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR 677C>T) POLYMORPHISM ON PLASMA HOMOCYSTEINE CONCENTRATIONS IN HEALTHY CHILDREN IS INFLUENCED BY CONSUMPTION OF FOLATE-FORTIFIED FOODS. NUTRITION. 26, 969-974.
  102. PAPOUTSAKIS C., YIANNAKOURIS N., MANIOS Y., PAPACONSTANTINOU E., MAGKOS F., SCHULPIS K., ZAMPELAS A., and MATALAS A. (2006) THE EFFECT OF MTHFR (C677T) GENOTYPE ON PLASMA HOMOCYSTEINE CONCENTRATIONS IN HEALTHY CHILDREN IS INFLUENCED BY GENDER. EUROPEAN JOURNAL OF CLINICAL NUTRITION. 60, 155-162.
  103. PAPOUTSAKIS C., YIANNAKOURIS N., MANIOS Y., PAPACONSTANTINOU E., MAGKOS F., SCHULPIS K., ZAMPELAS A., and MATALAS A. (2005) PLASMA HOMOCYSTEINE CONCENTRATIONS IN GREEK CHILDREN ARE INFLUENCED BY AN INTERACTION BETWEEN THE METHYLENETETRAHYDROFOLATE REDUCTASE C677T GENOTYPE AND FOLATE STATUS. JOURNAL NUTRITION. 135, 383-388.
  104. PARRI V., KATZAKI E., ULIANA V., SCIONTI F., TITA R., ARTUSO R., LONGO I., BOSCHLOO R., VIJZELAAR R., SELICORNI A., BRANCATI F., DALLAPICCOLA B., ZELANTE L., HAMEL C., SARDA P., LALANI S., GRASSO R., BUONI S., HAYEK J., SERVAIS L., DE VRIES B., GEORDOUDI N., NAKOU S., PETERSEN M., MARI F., RENIERI A., and ARIANI F. (2010) HIGH FREQUENCY OF COH1 INTRAGENIC DELETIONS AND DUPLICATIONS DETECTED BY MLPA IN PATIENTS WITH COHEN SYNDROME. EUROPEAN JOURNAL OF HUMAN GENETICS. 18, 1133-1140.
  105. PARTHIMOS T., SCHULPIS K., ANGELOGIANNI P., TSOPANAKIS C., PARTHIMOS N., and TSAKIRIS S. (2008) THE IN VIVO AND IN VITRO EFFECTS OF L-CARNITINE SUPPLEMENTATION ON THE ERYTHROCYTE MEMBRANE ACETYLCHOLINESTERASE, Na+, K+ -ATPase AND Mg2+ -ATPase ACTIVITIES IN BASKETBALL PLAYERS. CLIN CHEM LAB MED. 46(1), 137-142.
  106. PARTHIMOS T., TSOPANAKIS C., ANGELOGIANNI P., SCHULPIS K., PARTHIMOS N., and TSAKIRIS S. (2007) L-CYSTEINE SUPPLEMENTATION PREVENTS EXERCISE-INDUCED ALTERATIONS IN HUMAN ERYTHROCYTE MEMBRANE ACETYLCHOLINESTERASE AND Na+, K+ -ATPase ACTIVITIES. CLIN CHEM LAB MED. 45(1), 67-72.
  107. PARTHIMOS T., TSOPANAKIS C., ANGELOGIANNI P., SCHULPIS K., PARTHIMOS N., and TSAKIRIS S. (2007) THE EFFECT OF BASKETBALL TRAINING ON THE PLAYERS' ERYTHROCYTE MEMBRANE ACETYLCHOLINESTERASE, (NA+, K+) -ATPase AND Mg2+ -ATPase ACTIVITIES. INT J SPORTS MED. 28, 650-654.
  108. PATRINOS G. and PETERSEN M. (2009) COPY NUMBER VARIATION AND GENOMIC ALTERATIONS IN HEALTH AND DISEASE. GENOME MEDICINE. 1(2), 1-4.
  109. PATRINOS G., AL AAMA J., AL AQEEL A., AL-MULLA F., BORG J., DEVEREUX A., FELICE A., MACRAE F., MARAFIE M., PETERSEN M., QI M., RAMESAR S., ZLOTOGORA J., and COTTON R. (2011) RECOMMENDATIONS FOR GENETIC VARIATION DATA CAPTURE IN DEVELOPING COUNTRIES TO ENSURE A COMPREHENSIVE WORLDWIDE DATA COLLECTION. HUMAN MUTATION. 32, 2-9.
  110. PATRINOS G., VAN BAAL S., PETERSEN M., and PAPADAKIS M. (2005) HELLENIC NATIONAL MUTATION DATABASE: A PROTOTYPE DATABASE FOR MUTATIONS LEADING TO INHERITED DISORDERS IN THE HELLENIC POPULATION. HUMAN MUTATION. 25, 327-333.
  111. PECHLIVANI F., VASSILAKOU T., SARAFIDOU J., ZACHOU T., ANASTASIOU C., and SIDOSSIS L. (2006) PREVALENCE AND DETERMINANTS OF EXCLUSIVE BREASTFEEDING DURING HOSPITAL STAY IN GREECE. ACTA PAEDIATRICA.
  112. PEITSIDIS P., MANOLAKOS E., PEITSIDOU A., PETERSEN M., TSOPLOU P., KADIR R., and AGAPITOS E. (2009) PENTASOMY 49,XXXXY DIAGNOSED IN UTERO: CASE REPORT AND SYSTEMATIC REVIEW OF ANTENATAL FINDINGS. FETAL DIAGNOSIS AND THERAPY. 26, 1-5.
  113. PERRAULT I., HANEIN S., GERARD X., DELPHIN N., FARES-TAIE L., GERBER S., PELLETIER V., MERCE E., DOLLFUS H., PUECH B., DEFOORT-DHELLEMMES S., PETERSEN M.B., ZAFEIRIOU D., MUNNICH A., KAPLAN J., ROCHE O., and ROZET J.-M. (2010) SPECTRUM OF SPATA7 MUTATIONS IN LEBER CONGENITAL AMAUROSIS AND DELINEATION OF THE ASSOCIATED PHENOTYPE. HUMAN MUTATION. 31, E1241-E1250.
  114. PETERSEN M., KITSOS G., SAMPLES J., GAUDETTE N., ECONOMOU-PETERSEN E., SYKES R., RUST K., GRIGORIADOU M., APERIS G., CHOI D., PSILAS K., CRAIG J., KRAMER P., MACKEY D., and WIRTZ M. (2006) A LARGE GLC1C GREEK FAMILY WITH A MYOCILIN T377M MUTATION: INHERITANCE AND PHENOTYPIC VARIABILITY. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (IOVS). 47(2), 620-625.
  115. PETERSEN M.B. and WILLEMS P.J. (2006) NON-SYNDROMIC, AUTOSOMAL-RECESSIVE DEAFNESS. CLIN GENET. 69, 371-392.  
  116. PETERSEN M.B., WANG Q., and WILLEMS P.J. (2008) SEX-LINKED DEAFNESS. CLIN GENET. 73, 14-23.
  117. PRASSOULI A., ANTONIADOU I., KATSAROU E., ATTILAKOS A., SARAFIDOU J., MASTROYIANNI S., VOUDRIS K., SCARDOUTSOU A., and KONSTANTOPOULOS A. (2008) EVALUATION OF LEARNING DIFFICULTIES IN EPILEPTIC CHILDREN WITH IDIOPATHIC GENERALIZED EPILEPSY AND WELL-CONTROLLEDS SEIZURES. PEDIATRICS. 121(SUPPL.), S102.
  118. PRASSOULI A., ATTILAKOS A., KATSAROU E., SARAFIDOU J., MASTROYIANNI S., VOUDRIS K., SKARDOUTSOU A., and ANTONIADOU I. (2008) BEHAVIOURAL AND EMOTIONAL PROBLEMS IN CHILDREN WITH IDIOPATHIC GENERALIZED EPILEPSY AND WELL-CONTROLLED SEIZURES. ΠΑΙΔΙΑΤΡΙΚΗ. 71(3), 210-214.
  119. PRASSOULI A., KATSAROU E., ATTILAKOS A., and ANTONIADOU I. (2007) LEARNING DIFFICULTIES IN CHILDREN WITH EPILEPSY WITH IDIOPATHIC GENERALIZED EPILEPSY AND WELL-CONTROLLED SEIZURES. DEV MED CHILD NEUROL. 49(11), 874.
  120. PRASSOULI A., KATSAROU E., ATTILAKOS A., SARAFIDOU J., MASTROYIANNI S., VOUDRIS K., SCARDOUTSOU A., KONSTANTOPOULOS A., and ANTONIADOU I. (2008) BEHAVIORAL AND EMOTIONAL PROBLEMS IN EPILEPTIC CHILDREN WITH IDIOPATHIC EPILEPSY AND WELL-CONTROLLED SEIZURES. PEDIATRICS. 121(SUPPL.), S148.
  121. PRASSOULI A., PANAGIOTOU J., VAKAKI M., GIANNATOU I., ATTILAKOS A., GAROUFI A. and PAPAEVANGELOU V. (2007) ACUTE ACALCULOUS CHOLECYSTITIS AS THE INITIAL PRESENTATION OF PRIMARY EPSTEIN-BARR VIRUS INFECTION. J PEDIATR SURG. 42(1), E 11-3.
  122. SABOURDY F., MICHELAKAKIS H., ANASTASAKIS A., GARCIA V., MAVRIDOU I., NIETO M., PONS M.-C., SKIADAS C., MORAITOU M., MANTA P., ELLEDER M., and LEVADE T. (2009) DANON DISEASE: FURTHER CLINICAL AND MOLECULAR HETEROGENEITY. MUSCLE & NERVE. 39, 837-844.
  123. SANTAMARIA R., MICHELAKAKIS H., MORAITOU M., DIMITRIOU E., DOMINISSINI S., GROSSI S., SANCHEZ-OLLE G., CHABAS A., PITTIS M.G., FILOCAMO M., VILAGELIU L., and GRINBERG D. (2008) HAPLOTYPE ANALYSIS SUGGESTS A SINGLE BALKAN ORIGIN FOR THE GAUCHER DISEASE [D409H; H255Q] DOUBLE MUTANT ALLELE. HUMAN MUTATION. 29(6), E58-67.
  124. SARRI C., GYFTODIMOU Y., GRIGORIADOU M., PANTELIA E., KALOGIROU S., KOKOTAS H., MRASEK K., WEISE A., and PETERSEN M. (2006) SUPERNUMERARY MARKER CHROMOSOME 5 DIAGNOSED BY M-FISH IN A CHILD WITH CONGENITAL HEART DEFECT AND UNUSUAL FACE. CYTOGENETIC AND GENOME RESEARCH. 114, 330-337.
  125. SCHULPIS K., BARTZELIOTOU A., TSAKIRIS S., GOUNARIS A., and PAPASSOTIRIOU I. (2007) SERUM PARAOXONASE / ARYLESTERASE ACTIVITIES IN PHENYLKETONURIC PATIENTS ON DIET. EUROPEAN JOURNAL OF CLINICAL NUTRITION. 61, 803-808.
  126. SCHULPIS K., BARZELIOTOU A., PAPADAKIS M., RODOLAKIS A., ANTSAKLIS A., PAPASSOTIRIOU I., and VLACHOS G. (2008) MATERNAL CHRONIC HEPATITIS B VIRUS IS IMPLICATED WITH LOW NEONATAL PARAOXONASE/ARYLESTERASE ACTIVITIES. CLINICAL BIOCHEMISTRY. 41, 282-287.
  127. SCHULPIS K., GAVRILI S., VLACHOS G., KARIKAS G., MICHALAKAKOU K., DEMETRIOU E., and PAPASSOTIRIOU I. (2006) THE EFFECT OF NUTRITIONAL HABITS ON MATERNAL-NEONATAL LIPID AND LIPOPROTEIN SERUM LEVELS IN THREE DIFFERENT ETHNIC GROUPS. ANNALS OF NUTRITION & METABOLISM. 50, 290-296.
  128. SCHULPIS K., GIANNOULIA-KARANTANA A., PAPACONSTANTINOU E., PARTHIMOS T., TJAMOURANIS I., and TSAKIRIS S. (2006) ERYTHROCYTE MEMBRANE Na+, K+ -ATPase AND Mg2+ -ATPase ACTIVITIES IN SUBJECTS WITH METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) GENOTYPE AND MODERATE HYPERHOMOCYSTEINAEMIA. THE ROLE OF L-PHENYLALANINET®677 C AND L-ALANINE. CLIN CHEM LAB MED. 44(4), 423-427.
  129. SCHULPIS K., KALIMERIS K., BAKOGIANNIS C., TSAKIRIS T., and TSAKIRIS S. (2006) THE EFFECT OF IN VITRO HOMOCYSTINURIA ON THE SUCKLING RAT HIPPOCAMPAL ACETYLCHOLINESTERASE. METAB BRAIN DIS. 21, 21-28.
  130. SCHULPIS K., KARAKONSTANTAKIS T., VLACHOS G., GAVRILI S., MENTIS A.-F., LAZAROPOULOU C., and PAPASSOTIRIOU I. (2009) THE EFFECT OF NUTRITIONAL HABITS ON MATERNAL - NEONATAL ZINC AND MAGNESIUM LEVELS IN GREEKS AND ALBANIANS. EUROPEAN e-JOURNAL OF CLINICAL NUTRITION AND METABOLISM. 4, 176-180.
  131. SCHULPIS K., KARIKAS G., BARTZELIOTOU A., PAPAKONSTANTINOU E., KALOGERAKOU M., and TSAKIRIS S. (2007) THE EFFECT OF DIET ON PARAOXONASE 1/ARYLESTERASE ACTIVITIES IN PATIENTS WITH DISORDERS OF GALACTOSE METABOLISM. CLINICAL ENDOCRINOLOGY. 67, 687-692.
  132. SCHULPIS K., LAZAROPOULOU C., REGOUTAS S., KARIKAS G., MARGELI A., TSAKIRIS S., and PAPASSOTIRIOU I. (2006) VALPROIC ACID MONOTHERAPY INDUCES DNA OXIDATIVE DAMAGE. TOXICOLOGY. 217, 228-232.
  133. SCHULPIS K., LAZAROPOULOU C., VLACHOS G., PARTSINEVELOS G., MICHALAKAKOU K., GAVRILI S., GOUNARIS A., ANTSAKLIS A., and PAPASSOTIRIOU I. (2007) MATERNAL-NEONATAL 8-HYDROXY-DEOXYGUANOSINE SERUM CONCENTRATIONS AS AN INDEX OF DNA OXIDATION IN ASSOCIATION WITH THE MODE OF LABOUR AND DELIVERY. ACTA OBSTETRICIA ET GYNECOLOGICA. 86, 320-326.
  134. SCHULPIS K., MARGELI A., AKALESTOS A., VLACHOS G., PARTSINEVELOS G., PAPASTAMATAKI M., ANTSAKLIS A., and PAPASSOTIRIOU I. (2006) EFFECTS OF MODE OF DELIVERY ON MATERNAL-NEONATAL PLASMA ANTIOXIDANT STATUS AND ON PROTEIN S100B SERUM CONCENTRATIONS. SCAND J CLIN LAB INVEST. 66, 733-742.
  135. SCHULPIS K., MICHELAKAKIS H., TSAKIRIS T., and TSAKIRIS S. (2005) THE EFFECT OF DIET ON TOTAL ANTIOXIDANT STATUS, ERYTHROCYTE MEMBRANE NA+, K+ -ATPase ACTIVITIES IN PATIENTS WITH CLASSICAL GALACTOSAEMIA. CLINICAL NUTRITION. 24, 151-157.
  136. SCHULPIS K., MOUKAS M., PARTHIMOS T., TSAKIRIS T., PARTHIMOS N., and TSAKIRIS S. (2007) THE EFFECT OF α-TOCOPHEROL SUPPLEMENTATION ON TRAINING-INDUCED ELEVATION OF S100B PROTEIN IN SERA OF BASKETBALL PLAYERS.CLINICAL BIOCHEMISTRY. 40, 900-906.
  137. SCHULPIS K., PAPAKONSTANTINOU E., VLACHOS G., VLACHOS D., ANTSAKLIS A., PAPASSOTIRIOU I., and TSAKIRIS S. (2008) THE EFFECT OF THE MODE OF DELIVERY ON THE MATERNAL-NEONATAL CARNITINE BLOOD LEVELS AND ANTIOXIDANT STATUS. CLIN CHEM LAB MED. 46(5), 680-686.
  138. SCHULPIS K., PAPASSOTIRIOU I., and TSAKIRIS S. (2006) 8-HYDROXY-2-DESOXYGUANOSINE SERUM CONCENTRATIONS AS A MARKER OF DNA DAMAGE IN PATIENTS WITH CLASSICAL GALACTOSAEMIA. ACTA PAEDIATRICA. 95, 164-169.
  139. SCHULPIS K., PAPASSOTIRIOU I., PARTHIMOS T., TSAKIRIS T., and TSAKIRIS S. (2006) THE EFFECT OF L-CYSTEINE AND GLUTATHIONE ON INHIBITION OF Na+, K+ -ATPase ACTIVITY BY ASPARTAME METABOLITES IN HUMAN ERYTHROCYTE MEMBRANE. EUROPEAN JOURNAL OF CLINICAL NUTRITION. 60, 593-597.
  140. SCHULPIS K., PAPASSOTIRIOU I., TSAKIRIS S., VOUNATSOU M., and CHROUSOS G. (2005) INCREASED PLASMA ADIPONECTIN CONCENTRATIONS IN POORLY CONTROLLED PATIENTS WITH PHENYLKETONURIA NORMALIZE WITH A STRICT DIET: EVIDENCE FOR CATECHOLAMINE-MEDIATED ADIPONECTIN REGULATION AND A COMPLEX EFFECT OF PHENYLKETONURIA DIET ON ATHEROGENESIS RISK FACTORS. METABOLISM CLINICAL AND EXPERIMENTAL. 54, 1350-1355.
  141. SCHULPIS K., PAPASTAMATAKI M., STAMOU H., PAPASSOTIRIOU I., and MARGELI A. (2010) THE EFFECT OF DIET ON TOTAL ANTIOXIDANT STATUS, CERULOPLASMIN, TRANSFERRIN AND FERRITIN SERUM LEVELS IN PHENYLKETONURIC CHILDREN. ACTA PAEDIATRICA. 99, 1565-1570.
  142. SCHULPIS K., PARTHIMOS T., PAPAKONSTANTINOU E., TSAKIRIS T., PARTHIMOS N., MENTIS A.-F., and TSAKIRIS S. (2009) EVIDENCE FOR THE PARTICIPATION OF THE STIMULATED SYMPATHETIC NERVOUS SYSTEM IN THE REGULATION OF CARNITINE BLOOD LEVELS OF SOCCER PLAYERS DURING A GAME. METABOLISM CLINICAL AND EXPERIMENTAL. 58, 1080-1086.
  143. SCHULPIS K., PARTHIMOS T., TSAKIRIS T., PARTHIMOS N., and TSAKIRIS S. (2007) AN IN VIVO AND IN VITRO STUDY OF ERYTHROCYTE MEMBRANE ACETYLCHOLINESTERASE, (Na+, K+) -ATPase AND Mg2+ -ATPase ACTIVITIES IN BASKETBALL PLAYERS ON α-TOCOPHEROL SUPPLEMENTATION. THE ROLE OF L-CARNITINE. CLINICAL NUTRITION. 26, 63-69.
  144. SCHULPIS K., RECLOS G., PARTHIMOS T., PARTHIMOS N., GAVRIILIDIS A., and TSAKIRIS S. (2006) L-CYSTEINE SUPPLEMENTATION PROTECTS THE ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY FROM REDUCTION INDUCED BY FORCED TRAINING. CLINICAL BIOCHEMISTRY. 39, 1002-1006.
  145. SCHULPIS K., TSAKIRIS S., TRAEGER-SYNODINOS J., and PAPASSOTIRIOU I. (2005) LOW TOTAL ANTIOXIDANT STATUS IS IMPLICATED WITH HIGH 8-HYDROXY-2-DEOXYGUANOSINE SERUM CONCENTRATIONS IN PHENYLKETONURIA. CLINICAL BIOCHEMISTRY. 38, 239-242.
  146. SCHULPIS K., TSIRONI M., SKENDERI K., LAZAROPOULOU C., PARTHIMOS N., RECLOS G., GOUSSETIS E., TSAKIRIS S., and PAPASSOTIRIOU I. (2008) DRAMATIC REDUCTION OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY IN ATHLETES PARTICIPATING IN THE ULTRADISTANCE FOOT RACE "SPARTATHLON". THE SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION. 68(3), 228-232.
  147. SCHULPIS K., VLACHOS G., KARIKAS G., PAPAKONSTANTINOU E., VLACHOS D., PAPASSOTIRIOU I., ANTSAKLIS A., and TSAKIRIS S. (2008) THE EFFECT OF THE MODE OF DELIVERY ON MATERNAL-NEONATAL INTERLEUKIN-6, BIOGENIC AMINE AND THEIR PRECURSOR AMINO ACID CONCENTRATIONS. CLIN CHEM LAB MED. 46(11), 1624-1630.
  148. SCHULPIS K., VLACHOS G., PAPAKONSTANTINOU E., KARIKAS G., VLACHOS D., ROMA E., ANTSAKLIS A., PAPASSOTIRIOU I., and TSAKIRIS S. (2009) MATERNAL-NEONATAL AMINO ACID BLOOD LEVELS IN RELATION TO THE MODE OF DELIVERY. ACTA OBSTETRICIA ET GYNECOLOGICA. 88, 71-76.
  149. SIFAKIS S., KOUKOURA O., MANTAS N., PAPADOPOULOU E., GRIGORIADOU M., HAJIIOANNOU J., VLAHAKIS G., and PETERSEN M. (2011) ANTENATAL DIAGNOSIS OF DUODENAL ATRESIA IN DIZYGOTIC TWINS ASSOCIATED WITH CONGENITAL HEARING IMPAIRMENT.THE JOURNAL OF MATERNAL-FETAL AND NEONATAL MEDICINE.
  150. SIMINTZI I., SCHULPIS K., ANGELOGIANNI P., LIAPI C., and TSAKIRIS S. (2008) L-CYSTEINE AND GLUTATHIONE RESTORE THE MODULATION OF RAT FRONTAL CORTEX NA+, K+ -ATPase ACTIVITY INDUCED BY ASPARTAME METABOLITES. FOOD AND CHEMICAL TOXICOLOGY. 46, 2074-2079.
  151. SIMINTZI I., SCHULPIS K., ANGELOGIANNI P., LIAPI C., and TSAKIRIS S. (2007) L-CYSTEINE AND GLUTATHIONE RESTORE THE REDUCTION OF RAT HIPPOCAMPAL Na+, K+ -ATPase ACTIVITY INDUCED BY ASPARTAME METABOLITES. TOXICOLOGY. 237, 177-183.
  152. SIMINTZI I., SCHULPIS K., ANGELOGIANNI P., LIAPI C., and TSAKIRIS S. (2007) THE EFFECT OF ASPARTAME METABOLISM ON THE SUCKLING RAT FRONTAL CORTEX ACETYLCHOLINESTERASE. AN IN VITRO STUDY. FOOD AND CHEMICAL TOXICOLOGY. 45, 2397-2401.
  153. SIMINTZI I., SCHULPIS K., ANGELOGIANNI P., LIAPI C., and TSAKIRIS S. (2007) THE EFFECT OF ASPARTAME ON ACETYLCHOLINESTERASE ACTIVITY IN HIPPOCAMPAL HOMOGENATES OF SUCKLING RATS. PHARMACOLOGICAL RESEARCH. 56, 155-159.
  154. SIRMACI A., ERBEK S., PRICE J., HUANG M., DUMAN D., BASAK CENGIZ F., BADEMCI G., TOKGOZ-YILMAZ S., HISMI B., OZDAG H., OZTURK B., KULAKSIZOGLU S., YILDIRIM E., KOKOTAS H., GRIGORIADOU M., PETERSEN M.B., SHAHIN H., KANAAN M., KING M.-C., CHEN Z.-Y., BLANTON S., LIU X., ZUCHNER S., AKAR N., and TEKIN M. (2010) A TRUNCATING MUTATION IN SERPINB6 IS ASSOCIATED WITH AUTOSOMAL-RECESSIVE NONSYNDROMIC SENSORINEURAL HEARING LOSS. THE AMERICAN JOURNAL OF HUMAN GENETICS. 86, 797-804.
  155. SPENGOS K., MICHELAKAKIS H., VONTZALIDIS A., ZOUVELOU V., and MANTA P. (2009) DIABETES MELLITUS ASSOCIATED WITH GLYCOGEN STORAGE DISEASE TYPE III. MUSCLE & NERVE. 39, 876-877.
  156. THYS M., VAN DEN BOGAERT K., ILIADOU V., VANDERSTRAETEN K., DIELTJENS N., SCHRAUWEN I., CHEN W., ELEFTHERIADES N., GRIGORIADOU M., JAN PAUW R., CREMERS C., SMITH R., PETERSEN M., and VAN CAMP G. (2007) A SEVENTH LOCUS FOR OTOSCLEROSIS, OTSC7, MAPS TO CHROMOSOME 6q13 - 16.1. EUROPEAN JOURNAL OF HUMAN GENETICS. 15, 362-368.
  157. TOURNIS S., GIANNIKOU P., PASPATI I., KATSALIRA E., VOSKAKI I., and LYRITIS G. (2005) CO-EXISTENCE OF X-LINKED HYPOPHOSPHATEMIC RICKETS (XLH) AND PRIMARY HYPERPARATHYROIDISM: CASE REPORT REVIEW OF THE LITERATURE.J. MUSCULOSKELET NEURONAL INTERACT. 150-4.
  158. TSAKIRIS S., CARAGEORGIOU H., and SCHULPIS K. (2005) THE PROTECTIVE EFFECT OF L-CYSTEINE AND GLUTATHIONE ON THE ADULT AND AGED RAT BRAIN (NA+, K+) -ATPase AND Mg2+ -ATPase ACTIVITIES IN GALACTOSEMIA IN VITRO. METABOLIC BRAIN DISEASE. 20 (1), 87-95.
  159. TSAKIRIS S., GIANNOULIA-KARANTANA A., SIMINTZI I., and SCHULPIS K. (2006) THE EFFECT OF ASPARTAME METABOLITES ON HUMAN ERYTHROCYTE MEMBRANE ACETYLCHOLINESTERASE ACTIVITY. PHARMACOLOGICAL RESEARCH. 53, 1-5.
  160. TSAKIRIS S., KARIKAS G., PARTHIMOS T., TSAKIRIS T., BAKOGIANNIS C., and SCHULPIS K. (2009) ALPHA-TOCOPHEROL SUPPLEMENTATION PREVENTS THE EXERCISE-INDUCED REDUCTION OF SERUM PARAOXONASE 1/ARYLESTERASE ACTIVITIES IN HEALTHY INDIVIDUALS. EUROPEAN JOURNAL OF CLINICAL NUTRITION. 63, 215-221.
  161. TSAKIRIS S., MICHELAKAKIS H., and SCHULPIS K. (2005) ERYTHROCYTE MEMBRANE ACETYLCHOLINESTERASE, Na+, K+-ATPase AND Mg2+-ATPase ACTIVITIES IN PATIENTS WITH CLASSICAL GALACTOSAEMIA. ACTA PAEDIATRICA. 94, 1223-1226.
  162. TSAKIRIS S., PARTHIMOS T., PARTHIMOS N., TSAKIRIS T., and SCHULPIS K. (2006) THE BENEFICIAL EFFECT OF L-CYSTEINE SUPPLEMENTATION ON DNA OXIDATION INDUCED BY FORCED TRAINING. PHARMACOLOGICAL RESEARCH. 58, 386-390.
  163. TSAKIRIS S., PARTHIMOS T., RECLOS G., PARTHIMOS N., TSAKIRIS T., and SCHULPIS K. (2009) SIGNIFICANT REDUCTION OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY IN SOCCER-PLAYERS DURING PLAY. EVIDENCE FOR CATECHOLAMINE MEDIATED ENZYME INHIBITION. CLIN CHEM LAB MED. 47(5), 621-624.
  164. TSAKIRIS S., PARTHIMOS T., TSAKIRIS T., PARTHIMOS N., and SCHULPIS K. (2006) α-TOCOPHEROL SUPPLEMENTATION REDUCES THE ELEVATED 8-HYDROXY-2-DEOXYGUANOSINE BLOOD LEVELS INDUCED BY TRAINING IN BASKETBALL PLAYERS. CLI CHEM LAB MED. 44(8).
  165. TSAKIRIS S., RECLOS G., PARTHIMOS T., TSAKIRIS T., PARTHIMOS N., and SCHULPIS K. (2006) α-TOCOPHEROL SUPPLEMENTATION RESTORES THE REDUCTION OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY INDUCED BY FORCED TRAINING. PHARMACOLOGICAL RESEARCH. 54, 373-379.
  166. TSAKIRIS S., SCHULPIS K., PAPACONSTANTINOU E., TSAKIRIS T., TJAMOURANIS I., and GIANNOULIA-KARANTANA A. (2006) ERYTHROCYTE MEMBRANE ACETYLCHOLINESTERASE ACTIVITY IN SUBJECTS WITH MTHFR T GENOTYPE.à677C  CLIN CHEM LAB MED. 44(1), 23-27.
  167. TSAKIRIS T., ANGELOGIANNI P., TESSEROMATIS C., TSAKIRIS S., and SCHULPIS K. (2009) L-CYSTEINE'S EFFECT ON MODULATED RAT BRAIN ENZYMES WITH FORCED SWIMMING. INTERNATIONAL JOURNAL OF SPORT NUTRITION AND EXERCISE METABOLISM. 19, 285-297.
  168. TSAKIRIS T., ANGELOGIANNI P., TESSEROMATIS C., TSAKIRIS S., and SCHULPIS K. (2008) EFFECT OF L-CARNITINE ADMINISTRATION ON THE MODULATED RAT BRAIN PROTEIN CONCENTRATION, ACETYLCHOLINESTERASE, Na+K+-ATPase AND Mg2+-ATPase ACTIVITIES INDUCED BY FORCED SWIMMING. BR J SPORTS MED. 42, 367-372.
  169. VLACHOS D., SCHULPIS K., ANTSAKLIS A., MESOGITIS S., BILIATIS I., and TSAKIRIS S. (2010) ERYTHROCYTE MEMBRANE AChE, Na+, K+ -ATPase AND Mg2+ ATPase ACTIVITIES IN MOTHERS AND THEIR PREMATURE NEONATES IN RELATION TO THE MODE OF DELIVERY. SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION. 70, 568-574.
  170. VLACHOS D., SCHULPIS K., PARTHIMOS T., MESOGITIS S., VLACHOS G., ANTSAKLIS A., and TSAKIRIS S. (2008) MATERNAL-NEONATAL ERYTHROCYTE MEMBRANE Na+, K+ -ATPase AND Mg2+ -ATPase ACTIVITIES IN RELATION TO THE MODE OF DELIVERY. EUR J APPL PHYSIOL. 103, 501-508.
  171. VLACHOS D., SCHULPIS K., PARTHIMOS T., MESOGITIS S., VLACHOS G., PARTSINEVELOS G., ANTSAKLIS A., and TSAKIRIS S. (2008) THE EFFECT OF THE MODE OF DELIVERY ON THE MATERNAL-NEONATAL ERYTHROCYTE MEMBRANE ACETYLCHOLINESTERASE ACTIVITY. CLINICAL BIOCHEMISTRY. 41, 818-823.
  172. VLACHOS G., BARTZELIOTOU A., SCHULPIS K., PARTSINEVELOS G., LAZAROPOULOU C., PAPADIMA C., PAPASTAMATAKI M., ANTSAKLIS A., and PAPASSOTIRIOU I. (2006) MATERNAL-NEONATAL SERUM PARAOXONASE 1 ACTIVITY IN RELATION TO THE MODE OF DELIVERY. CLINICAL BIOCHEMISTRY. 39, 923-928.
  173. VLACHOS G., SCHULPIS K., PAPAKONSTANTINOU E., PAPADAKIS M., ELEFSINIOTIS I., PAPASSOTIRIOU I., and ANTSAKLIS A. (2008) MATERNAL CHRONIC HEPATITIS B VIRUS DOES NOT AFFECT NEONATAL BIOTINIDASE ACTIVITY. ACTA PAEDIATRICA. 97 (3), 362-365.
  174. VOSKAKI I., ARVANITIDOU V., ATHANASOPOULOU H., TZAGKARAKI A., TRIPSIANIS G., and GIANNOULIA-KARANTANA A. (2010) SERUM COPPER AND ZINC LEVELS IN HEALTHY GREEK CHILDREN AND THEIR PARENTS. BIOLOGICALTRACE ELEMENTSRESEARCH. 134 (2), 136-145.
  175. WATTENHOFER M., REYMOND A., FALCIOLA V., CHAROLLAIS A., CAILLE D., BOREL C., LYLE R., ESTIVILL X., PETERSEN M., MEDA P., and ANTONARAKIS S. (2005) DIFFERENT MECHANISMS PRECLUDE MUTANT CLDN14 PROTEINS FROM FORMING TIGHT JUNCTIONS IN VITRO. HUMAN MUTATION. 25, 543-549.
  176. WHYTE M., SINGHELLAKIS P., PETERSEN M., DAVIES M., TOTTY W., and MUMM S. (2007) JUVENILE PAGET'S DISEASE: THE SECOND REPORTED, OLDEST PATIENT IS HOMOZYGOUS FOR THE TNFRSF11B "BALKAN" MUTATION (966_969 delTGACinsCTT), WHICH ELEVATES CIRCULATING IMMUNOREACTIVE OSTEOPROTEGERIN LEVELS. JOURNAL OF BONE AND MINERAL RESEARCH. 22(6), 938-946.
  177. WIRTZ M.K., KONSTAS A.G., SAMPLES J.R., KALTSOS K., ECONOMOU A., DIMOPOULOS A., GEORGIADOU I., and PETERSEN M.B. (2008) MYOCILIN VARIATIONS AND FAMILIAL GLAUCOMA IN TAXIARCHIS, A SMALL GREEK VILLAGE. MOL VIS. 14, 774-781.
  178. XAIDARA A., KARAVITAKIS E., KOSMA K., EMMA F., DIMITRIOU E., and MICHELAKAKIS H. (2009) CHITOTRIOSIDASE PLASMA ACTIVITY IN NEPHROPATHIC CYSTINOSIS. J INHER METAB DIS. 32, 577 DOI: 10. 1007/S10545-009-1118-8.
  179. YANG Z., KITSOS G., TONG Z., PAYNE M., GOREZIS S., PSILAS K., GRIGORIADOU M., ZHAO Y., KAMAYA S., APERIS G., PETERSEN M., and ZHANG K. (2006) A NOVEL LOCUS ON 19q13 ASSOCIATED WITH AUTOSOMAL-DOMINANT MACULAR DYSTROPHY IN A LARGE GREEK FAMILY. J MED GENET. 43(e57).
  180. ZAFEIRIOU D., VARGIAMI E., PAPADOPOULOU K., DIMITRIOU E., MAVRIDOU I., SANTAMARIA R., CANALS I., and MICHELAKAKIS H. (2008) SERIAL MAGNETIC RESONANCE IMAGING AND NEUROPHYSIOLOGICAL STUDIES IN MULTIPLE SULPHATASE DEFICIENCY. EUR J PAEDIATR NEUROL. 12(3), 190-194.
  181. ZOLLINO M., LECCE R., MURDOLO M., ORTESCHI D., MARANGI G., SELICORNI A., MIDRO A., SORGE G., ZAMPINO G., MEMO L., BATTAGLIA D., PETERSEN M., PANDELIA E., GYFTODIMOU Y., FARAVELLI F., TENCONI R., GARAVELLI L., MAZZANTI L., FISCHETTO R., CAVALLI P., SAVASTA S., RODRIGUEZ L., and NERI G. (2007) WOLF-HIRSCHHORN SYNDROME-ASSOCIATED CHROMOSOME CHANGES ARE NOT MEDIATED BY OLFACTORY RECEPTOR GENE CLUSTERS NOR BY INVERSION POLYMORPHISM ON 4p16. HUMAN GENETICS. 122, 423-430.
  182. ΒΑΙΡΑΜΗ Μ., ΒΟΡΡΙΑ Γ., ΚΙΟΣΕΟΓΛΟΥ Γ. (2005) ΠΑΡΑΓΟΝΤΕΣ ΠΟΥ ΣΧΕΤΙΖΟΝΤΑΙ ΜΕ ΤΗ ΔΗΜΟΤΙΚΟΤΗΤΑ ΚΑΙ ΤΙΣ ΦΙΛΙΕΣ ΤΩΝ ΠΑΙΔΙΩΝ ΚΑΙ ΤΩΝ ΕΦΗΒΩΝ ΣΤΟ ΠΛΑΙΣΙΟ ΤΟΥ ΣΧΟΛΕΙΟΥ. ΠΑΙΔΙ ΚΑΙ ΕΦΗΒΟΣ: ΨΥΧΙΚΗ ΥΓΕΙΑ ΚΑΙ ΨΥΧΟΠΑΘΟΛΟΓΙΑ. 7(2), 52-67.
  183. ΒΟΡΡΙΑ Π., ΣΑΡΑΦΙΔΟΥ Ε., ΠΑΠΑΛΗΓΟΥΡΑ Ζ., ΛΑΜΠΙΔΗ Α., ΚΟΝΤΟΠΟΥΛΟΥ Α. (2006) ΟΙ ΕΠΙΠΤΩΣΕΙΣ ΤΗΣ ΠΑΡΕΧΟΜΕΝΗΣ ΦΡΟΝΤΙΔΑΣ ΣΤΟ ΔΕΣΜΟ "ΜΗΤΕΡΑΣ" - ΒΡΕΦΟΥΣ ΣΕ ΒΡΕΦΗ ΤΟΥ ΚΕΝΤΡΟΥ ΒΡΕΦΩΝ "ΜΗΤΕΡΑ". ΨΥΧΟΛΟΓΙΑ. 13(2), 21-36.
  184. ΔΑΣΟΠΟΥΛΟΥ Μ., ΑΠΟΣΤΟΛΟΥ Μ., ΜΠΑΡΟΥΤΗΣ Γ., ΜΙΧΕΛΑΚΑΚΗ Ε., ΛΟΥΚΑΤΟΥ Ε., ΚΩΣΤΑΛΟΣ Χ. (2005) ΣΥΓΓΕΝΗΣ ΥΠΟΠΛΑΣΙΑ ΕΠΙΝΕΦΡΙΔΙΩΝ ΜΕ ΚΛΙΝΙΚΗ ΠΡΟΒΟΛΗ ΣΟΒΑΡΗΣ ΑΝΑΠΝΕΥΣΤΙΚΗΣ ΑΝΕΠΑΡΚΕΙΑΣ ΣΤΗ ΝΕΟΓΝΙΚΗ ΠΕΡΙΟΔΟ. ΠΕΡΙΓΡΑΦΗ ΠΕΡΙΠΤΩΣΗΣ. ΠΑΙΔΙΑΤΡΙΚΗ. 68, 150-153.
  185. ΚΑΛΗΜΕΡΗΣ Κ., ΣΟΥΛΠΗ Κ., ΤΣΑΚΙΡΗΣ Σ. (2005) Η ΕΥΘΥΝΗ ΤΩΝ ΕΛΕΥΘΕΡΩΝ ΡΙΖΩΝ ΣΤΗΝ ΕΜΦΑΝΙΣΗ ΝΕΥΡΟΕΚΦΥΛΙΣΤΙΚΩΝ ΝΟΣΗΜΑΤΩΝ. ΙΑΤΡΙΚΑ ΧΡΟΝΙΚΑ. ΚΗ(4), 209-217.
  186. ΚΑΛΗΜΕΡΗΣ Κ., ΣΟΥΛΠΗ Κ., ΚΑΜΠΟΥΡΟΓΛΟΥ Γ., ΤΣΑΚΙΡΗΣ Σ. (2005) Ο ΡΟΛΟΣ ΤΟΥ ΣΙΔΗΡΟΥ ΚΑΙ ΤΟΥ ΧΑΛΚΟΥ ΣΤΟ ΟΞΕΙΔΩΤΙΚΟ STRESS IN VIVO. ΧΗΜΙΚΑ ΧΡΟΝΙΚΑ. 9, 22-26.
  187. ΚΑΛΗΜΕΡΗΣ Κ., ΣΟΥΛΠΗ Κ., ΤΣΑΚΙΡΗΣ Θ., ΤΣΑΚΙΡΗΣ Σ. (2006) Η ΕΠΙΔΡΑΣΗ ΤΩΝ ΕΛΕΥΘΕΡΩΝ ΡΙΖΩΝ ΣΤΗ ΜΥΙΚΗ ΑΣΚΗΣΗ.ΧΗΜΙΚΑ ΧΡΟΝΙΚΑ. 3, 25-28.
  188. ΚΑΛΗΜΕΡΗΣ Κ., ΣΟΥΛΠΗ Κ., ΤΣΑΚΙΡΗΣ Θ., ΤΣΑΚΙΡΗΣ Σ. (2005) Η ΠΑΡΟΥΣΙΑ ΤΩΝ ΑΝΤΙΟΞΕΙΔΩΤΙΚΩΝ ΣΤΟ ΔΙΑΙΤΟΛΟΓΙΟ ΜΑΣ. ΔΙΑΤΡΟΦΗ-ΔΙΑΙΤΟΛΟΓΙΑ. 9(3-4), 79-88.
  189. ΚΑΜΠΟΥΡΟΓΛΟΥ Γ., ΣΟΥΛΠΗ Κ., ΚΑΛΗΜΕΡΗΣ Κ., ΤΣΑΚΙΡΗΣ Θ., ΚΑΡΙΚΑΣ Γ., ΤΣΑΚΙΡΗΣ Σ. (2005) Η ΕΠΙΔΡΑΣΗ ΤΗΣ ΚΑΡΝΙΤΙΝΗΣ ΣΤΗ ΝΕΥΡΟΠΑΘΟΛΟΓΙΑ ΤΟΥ ΕΓΚΕΦΑΛΟΥ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 18(IV), 114-119.
  190. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΓΥΦΤΟΔΗΜΟΥ ΚΟΡΡΕΣ Γ., ΦΕΡΕΚΥΔΟΥ Ε., ΚΑΝΔΗΛΩΡΟΣ Δ., PETERSEN M.B. (2010) ΕΝΤΟΝΕΣ ΦΑΙΝΟΤΥΠΙΚΕΣ ΔΙΑΒΑΘΜΙΣΕΙΣ ΣΕ ΜΙΑ ΟΙΚΟΓΕΝΕΙΑ ΜΕ ΜΙΑ ΜΙΤΟΧΟΝΔΡΙΑΚΗ ΚΑΙ ΜΙΑ ΠΥΡΗΝΙΚΗ ΜΕΤΑΛΛΑΓΗ ΒΑΡΗΚΟΙΑΣ. ΕΛΛΗΝΙΚΗ ΩΤΟΡΙΝΟΛΑΡΥΓΓΟΛΟΓΙΑ ΧΕΙΡΟΥΡΓΙΚΗ ΚΕΦΑΛΗΣ & ΤΡΑΧΗΛΟΥ. 31(1), 45-49.
  191. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΚΙΤΣΟΣ Γ., ΓΙΑΝΝΟΥΛΙΑ-ΚΑΡΑΝΤΑΝΑ Α., PETERSEN M.B. (2009) Η ΓΕΝΕΤΙΚΗ ΤΟΥ ΠΡΩΤΟΠΑΘΟΥΣ ΓΛΑΥΚΩΜΑΤΟΣ ΑΝΟΙΚΤΗΣ ΓΩΝΙΑΣ: ΜΕΤΑΛΛΑΓΕΣ ΚΑΙ ΓΟΝΙΔΙΑΚΟΙ ΤΟΠΟΙ. ΟΦΘΑΛΜΟΛΟΓΙΚΑ ΧΡΟΝΙΚΑ. 19(3), 242-245.
  192. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΚΟΡΡΕΣ Γ., ΓΙΑΝΝΟΥΛΙΑ-ΚΑΡΑΝΤΑΝΑ Α., PETERSEN M.B. (2009) ΤΟ ΜΙΤΟΧΟΝΔΡΙΟ, ΑΥΤΟΣ Ο ΜΙΚΡΟΣ ΔΑΙΜΟΝΑΣ. ΕΛΛΗΝΙΚΗ ΩΤΟΡΙΝΟΛΑΡΥΓΓΟΛΟΓΙΑ ΧΕΙΡΟΥΡΓΙΚΗ ΚΕΦΑΛΗΣ & ΤΡΑΧΗΛΟΥ. 26-31.
  193. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΚΟΡΡΕΣ Γ., ΓΙΑΝΝΟΥΛΙΑ-ΚΑΡΑΝΤΑΝΑ Α., PETERSEN M.B. (2008) Η ΣΗΜΑΝΤΙΚΟΤΗΤΑ ΤΩΝ ΜΕΤΑΛΛΑΓΩΝ ΤΟΥ ΓΟΝΙΔΙΟΥ GJB2 ΣΤΗ ΝΕΥΡΟΑΙΣΘΗΤΗΡΙΑ, ΜΗ ΣΥΝΔΡΟΜΙΚΗ, ΑΥΤΟΣΩΜΑΤΙΚΟΥ ΥΠΟΛΕΙΠΟΜΕΝΟΥ ΤΥΠΟΥ ΒΑΡΗΚΟΙΑ. ΕΛΛΗΝΙΚΗ ΩΤΟΡΙΝΟΛΑΡΥΓΓΟΛΟΓΙΑ ΧΕΙΡΟΥΡΓΙΚΗ ΚΕΦΑΛΗΣ & ΤΡΑΧΗΛΟΥ. 29(4), 177-181.
  194. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΚΟΡΡΕΣ Γ., ΦΕΡΕΚΥΔΟΥ Ε., ΓΙΑΝΝΟΥΛΙΑ-ΚΑΡΑΝΤΑΝΑ Α., ΚΑΝΔΗΛΩΡΟΣ Δ., PETERSEN M.B. (2009) ΑΠΩΛΕΙΑ ΑΚΟΗΣ ΩΣ ΑΠΟΤΕΛΕΣΜΑ ΤΩΝ ΜΕΤΑΛΛΑΓΩΝ ΤΟΥ ΜΙΤΟΧΟΝΔΡΙΑΚΟΥ DNA. ΕΛΛΗΝΙΚΗ ΩΤΟΡΙΝΟΛΑΡΥΓΓΟΛΟΓΙΑ ΧΕΙΡΟΥΡΓΙΚΗ ΚΕΦΑΛΗΣ & ΤΡΑΧΗΛΟΥ. 30(2), 74-81.
  195. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΚΟΡΡΕΣ Γ., ΦΕΡΕΚΥΔΟΥ Ε., ΓΥΦΤΟΔΗΜΟΥ Γ., ΓΙΑΝΝΟΥΛΙΑ-ΚΑΡΑΝΤΑΝΑ Α., ΚΑΝΔΗΛΩΡΟΣ Δ., PETERSEN M.B. (2009) ΝΕΥΡΟΑΙΣΘΗΤΗΡΙΑ, ΜΗ ΣΥΝΔΡΟΜΙΚΗ ΑΠΩΛΕΙΑ ΑΚΟΗΣ ΣΧΕΤΙΖΟΜΕΝΗ ΜΕ ΤΗ ΣΗΜΕΙΑΚΗ ΜΕΤΑΛΛΑΓΗ A7445G ΤΟΥ ΜΙΤΟΧΟΝΔΡΙΑΚΟΥ ΓΟΝΙΔΙΩΜΑΤΟΣ ΣΤΟΥΣ ΕΛΛΗΝΕΣ. ΕΛΛΗΝΙΚΗ ΩΤΟΡΙΝΟΛΑΡΥΓΓΟΛΟΓΙΑ ΧΕΙΡΟΥΡΓΙΚΗ ΚΕΦΑΛΗΣ & ΤΡΑΧΗΛΟΥ. 30(4), 145-148.
  196. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΚΟΡΡΕΣ Γ., ΦΕΡΕΚΥΔΟΥ Ε., ΚΑΝΔΗΛΩΡΟΣ Δ., PETERSEN M.B. (2010) ΑΝΙΧΝΕΥΣΗ ΜΕΤΑΛΛΑΓΩΝ ΤΟΥ ΠΥΡΗΝΙΚΟΥ ΓΟΝΙΔΙΟΥ GJB2 ΣΤΟΝ ΕΛΛΗΝΙΚΟ ΠΛΗΘΥΣΜΟ. ΕΛΛΗΝΙΚΗ ΩΤΟΡΙΝΟΛΑΡΥΓΓΟΛΟΓΙΑ ΧΕΙΡΟΥΡΓΙΚΗ ΚΕΦΑΛΗΣ & ΤΡΑΧΗΛΟΥ. 31(2), 45-48.
  197. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΚΟΡΡΕΣ Γ., ΦΕΡΕΚΥΔΟΥ Ε., ΠΑΠΑΔΟΠΟΥΛΟΥ Ε., ΝΕΟΥ Π., ΓΙΑΝΝΟΥΛΙΑ-ΚΑΡΑΝΤΑΝΑ Α., ΚΑΝΔΗΛΩΡΟΣ Δ., PETERSEN M.B. (2009) ΜΟΡΙΑΚΟΣ ΕΛΕΓΧΟΣ ΤΗΣ ΜΕΤΑΛΛΑΓΗΣ A1555G ΤΟΥ ΜΙΤΟΧΟΝΔΡΙΑΚΟΥ DNA ΣΤΗ ΝΕΥΡΟΑΙΣΘΗΤΗΡΙΑ, ΜΗ ΣΥΝΔΡΟΜΙΚΗ ΒΑΡΗΚΟΙΑ ΣΤΟΝ ΕΛΛΗΝΙΚΟ ΠΛΗΘΥΣΜΟ. ΕΛΛΗΝΙΚΗ ΩΤΟΡΙΝΟΛΑΡΥΓΓΟΛΟΓΙΑ ΧΕΙΡΟΥΡΓΙΚΗ ΚΕΦΑΛΗΣ & ΤΡΑΧΗΛΟΥ. 30(3), 103-107.
  198. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΠΑΠΑΓΕΩΡΓΙΟΥ Ε., ΓΙΑΝΝΟΥΛΙΑ-ΚΑΡΑΝΤΑΝΑ Α., PETERSEN M.B. (2009) Η ΦΥΛΟΣΥΝΔΕΤΗ ΝΕΑΝΙΚΗ ΡΕΤΙΝΟΣΧΙΣΗ: ΠΡΟΣΕΓΓΙΣΗ ΜΟΡΙΑΚΗΣ ΓΕΝΕΤΙΚΗΣ. ΟΦΘΑΛΜΟΛΟΓΙΚΑ ΧΡΟΝΙΚΑ. 19(4), 367-372.
  199. ΚΟΚΟΤΑΣ Χ., ΓΡΗΓΟΡΙΑΔΟΥ Μ., ΠΑΠΑΓΕΩΡΓΙΟΥ Ε., ΓΙΑΝΝΟΥΛΙΑ-ΚΑΡΑΝΤΑΝΑ Α., PETERSEN M.B. (2010) Η ΓΕΝΕΤΙΚΗ ΤΗΣ ΜΗ ΣΥΝΔΡΟΜΙΚΗΣ ΑΝΙΡΙΔΙΑΣ. ΟΦΘΑΛΜΟΛΟΓΙΚΑ ΧΡΟΝΙΚΑ. 1, 28-32.
  200. ΛΑΜΠΑΔΑΡΙΔΗΣ Ι., ΔΗΜΗΤΡΙΟΥ Ε., ΘΕΟΔΩΡΑΚΗ Μ., ΒΕΛΕΓΡΑΚΗ Α., ΚΑΦΑΛΙΔΗΣ Γ.,  ΜΙΧΕΛΑΚΑΚΗ Ε. (2006) Η ΧΙΤΟΤΡΙΟΖΙΔΑΣΗ ΣΕ ΝΕΟΓΝΑ ΜΕ ΣΥΣΤΗΜΑΤΙΚΗ ΜΥΚΗΤΙΑΣΗ ΚΑΙ ΚΟΙΝΕΣ ΜΙΚΡΟΒΙΑΚΕΣ ΛΟΙΜΩΞΕΙΣ. ΑΡΧΕΙΑ ΕΛΛΗΝΙΚΗΣ ΙΑΤΡΙΚΗΣ. 23(2), 173-177.
  201. ΛΟΥΜΑΚΟΥ Μ., ΣΑΡΑΦΙΔΟΥ Ε., ΚΟΡΔΟΥΤΗΣ Π., ΜΠΑΡΜΠΟΠΟΥΛΟΥ Δ. (2006) ΣΤΑΣΕΙΣ ΔΑΣΚΑΛΩΝ ΚΑΙ ΔΙΑΤΡΟΦΙΚΗ ΑΓΩΓΗ ΣΤΟ ΣΧΟΛΕΙΟ. ΜΕΝΤΟΡΑΣ: ΠΕΡΙΟΔΙΚΟ ΕΠΙΣΤΗΜΟΝΙΚΩΝ ΚΑΙ ΕΚΠΑΙΔΕΥΤΙΚΩΝ ΕΡΕΥΝΩΝ. 9, 43-59.
  202. ΜΑΝΩΛΑΚΗ Ν., ΜΗΤΣΙΚΑ Α., ΣΜΠΩΚΟΥ Δ., ΠΡΙΦΤΗΣ Κ., ΦΛΩΚΟΥ Α., ΜΙΧΕΛΑΚΑΚΗ Ε. (2006) ΝΟΣΟΣ NIEMANN-PICK ΤΥΠΟΥ Β ΜΕ ΣΠΑΝΙΟ ΓΟΝΟΤΥΠΟ - ΠΕΡΙΓΡΑΦΗ ΠΕΡΙΠΤΩΣΗΣ. ΠΑΙΔΙΑΤΡΙΚΗ. 69, 213-217.
  203. ΜΑΡΓΑΡΙΤΗΣ Μ., ΜΕΝΤΗΣ Α.-Φ., ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΤΣΑΚΙΡΗΣ Σ. (2009) Ο ΡΟΛΟΣ ΤΗΣ L-ΚΑΡΝΙΤΙΝΗΣ ΣΤΗΝ ΕΓΚΕΦΑΛΙΚΗ ΓΗΡΑΝΣΗ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 22 I, 20-29.
  204. ΜΑΡΓΑΡΙΤΗΣ Μ., ΜΕΝΤΗΣ Α.-Φ., ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΤΣΑΚΙΡΗΣ Σ. (2009) Ο ΡΟΛΟΣ ΤΗΣ L-ΚΑΡΝΙΤΙΝΗΣ ΣΤΙΣ ΝΕΥΡΟΕΚΦΥΛΙΣΤΙΚΕΣ ΔΙΑΤΑΡΑΧΕΣ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 22(II), 39-45.
  205. ΜΑΥΡΙΚΑ Π. (2008) ΑΓΩΓΗ ΥΓΕΙΑΣ ΣΤΗΝ ΚΟΙΝΟΤΗΤΑ: ΠΡΟΓΡΑΜΜΑ ΠΑΡΕΜΒΑΣΗΣ ΣΕ ΓΥΝΑΙΚΕΙΟ ΑΣΤΙΚΟ ΠΛΗΘΥΣΜΟ (30-60 ΕΤΩΝ) ΣΤΟΝ ΤΟΜΕΑ ΤΗΣ ΠΡΟΛΗΨΗΣ ΤΗΣ ΟΣΤΕΟΠΟΡΩΣΗΣ ΜΕΣΩ ΥΠΗΡΕΣΙΩΝ ΠΡΩΤΟΒΑΘΜΙΑΣ ΦΡΟΝΤΙΔΑΣ. ΝΕΑ ΥΓΕΙΑ. 62.
  206. ΜΙΧΑΗΛ Μ., ΣΑΒΒΙΔΟΥ Κ., ΧΟΝΔΡΟΜΑΤΙΔΟΥ Σ., ΜΙΧΕΛΑΚΑΚΗ Ε., ΦΙΤΣΙΩΡΗΣ Ξ., ΓΕΩΡΓΙΑΔΗΣ Γ. (2005) ΜΕΤΑΧΡΩΜΑΤΙΚΗ ΛΕΥΚΟΔΥΣΤΡΟΦΙΑ ΕΝΗΛΙΚΟΣ (ΔΙΑΦΟΡΟΔΙΑΓΝΩΣΤΙΚΑ ΠΡΟΒΛΗΜΑΤΑ). ΕΓΚΕΦΑΛΟΣ. 42, 82-86.
  207. ΜΙΧΕΛΑΚΑΚΗ Ε. (2006) ΝΟΣΟΣ FABRY: ΠΑΘΟΦΥΣΙΟΛΟΓΙΑ, ΔΙΑΓΝΩΣΗ ΚΑΙ ΘΕΡΑΠΕΙΑ. BIO HEALTH REPORTS. 16, 58-61.
  208. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΚΑΛΗΜΕΡΗΣ Κ., ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΠΑΡΘΥΜΟΣ Ν., ΤΣΑΚΙΡΗΣ Σ. (2007) Ο ΡΟΛΟΣ ΤΟΥ ΙΝΣΟΥΛΙΝΟΜΙΜΗΤΙΚΟΥ ΑΥΞΗΤΙΚΟΥ ΠΑΡΑΓΟΝΤΑ 1 (IGF-1) ΣΤΗΝ ΟΜΟΙΟΣΤΑΣΗ ΤΟΥ ΑΝΘΡΩΠΟΥ ΚΑΙ ΟΙ ΘΕΡΑΠΕΥΤΙΚΕΣ ΤΟΥ ΔΡΑΣΕΙΣ ΣΤΗ ΓΗΡΑΝΣΗ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 20, 1-10.
  209. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΣΟΥΛΠΗ Κ., ΤΣΑΚΙΡΗΣ Σ. (2006) Η ΕΠΙΔΡΑΣΗ ΤΗΣ ΘΕΡΑΠΕΥΤΙΚΗΣ ΧΟΡΗΓΗΣΗΣ ΤΟΥ ΒΑΛΠΡΟΙΚΟΥ ΟΞΕΟΣ (DEPAQUINE) ΣΤΗΝ ΠΑΡΑΓΩΓΗ ΕΛΕΥΘΕΡΩΝ ΡΙΖΩΝ. ΙΑΤΡΙΚΑ ΧΡΟΝΙΚΑ. ΚΘ(3), 182-186.
  210. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΣΟΥΛΠΗ Κ., ΤΣΑΚΙΡΗΣ Σ. (2007) Η ΕΠΙΔΡΑΣΗ ΤΟΥ ΤΡΟΠΟΥ ΖΩΗΣ ΣΤΗ ΔΡΑΣΤΙΚΟΤΗΤΑ ΤΗΣ ΠΑΡΑΟΞΟΝΑΣΗΣ. ΙΑΤΡΙΚΑ ΧΡΟΝΙΚΑ. ΚΙ(1), 40-45.
  211. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΣΟΥΛΠΗ Κ., ΤΣΑΚΙΡΗΣ Σ. (2006) Η ΕΥΕΡΓΕΤΙΚΗ ΕΠΙΔΡΑΣΗ ΤΗΣ ΒΙΤΑΜΙΝΗΣ Ε ΣΤΗ ΔΡΑΣΤΙΚΟΤΗΤΑ ΤΟΥ ΑΝΤΙΑΘΗΡΟΓΕΝΕΤΙΚΟΥ ΕΝΖΥΜΟΥ ΠΑΡΑΟΞΟΝΑΣΗ 1. ΔΙΑΤΡΟΦΗ-ΔΙΑΙΤΟΛΟΓΙΑ. 10(3-4), 73-77.
  212. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΣΟΥΛΠΗ Κ., ΤΣΑΚΙΡΗΣ Σ. (2008) Η ΣΧΕΣΗ ΦΑΡΜΑΚΩΝ ΚΑΙ ΟΞΕΙΔΩΤΙΚΟΥ ΣΤΡΕΣ ΜΕ ΤΟ ΕΝΖΥΜΟ ΠΑΡΑΟΞΟΝΑΣΗ 1. ΧΗΜΙΚΑ ΧΡΟΝΙΚΑ. 1, 18-19.
  213. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΤΣΑΚΙΡΗΣ Σ. (2005) ΕΠΙΛΗΨΙΑ ΚΑΙ ΕΓΚΥΜΟΣΥΝΗ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 18, 69-75.
  214. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΤΣΑΚΙΡΗΣ Σ. (2005) Η ΔΡΑΣΗ ΤΟΥ "ΑΛΚΟΟΛ" ΣΤΗΝ ΠΑΡΑΓΩΓΗ ΕΛΕΥΘΕΡΩΝ ΡΙΖΩΝ - ΘΕΡΑΠΕΥΤΙΚΗ ΑΝΤΙΜΕΤΩΠΙΣΗ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 18, 12-22.
  215. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΤΣΑΚΙΡΗΣ Σ. (2006) Η ΣΗΜΑΣΙΑ ΤΗΣ ΧΟΡΗΓΗΣΗΣ ΤΟΥ ΑΜΙΝΟΞΕΟΣ L-ΑΡΓΙΝΙΝΗ ΚΑΙ ΤΗΣ ΑΝΤΙΟΞΕΙΔΩΤΙΚΗΣ ΟΥΣΙΑΣ Ν-ΑΚΕΤΥΛΟΚΥΣΤΕΙΝΗ ΣΤΗ ΘΕΡΑΠΕΥΤΙΚΗ ΑΝΤΙΜΕΤΩΠΙΣΗ ΤΗΣ ΠΡΟΕΚΛΑΜΨΙΑΣ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 19(II), 37-43.
  216. ΜΠΑΚΟΓΙΑΝΝΗΣ Κ., ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΤΣΑΚΙΡΗΣ Σ. (2006) ΠΑΡΑΟΞΟΝΑΣΕΣ ΚΑΙ ΝΟΣΟΙ ΤΟΥ ΚΑΡΔΙΑΓΓΕΙΑΚΟΥ ΣΥΣΤΗΜΑΤΟΣ. ΕΠΙΔΡΑΣΕΙΣ ΑΠΟ ΦΑΡΜΑΚΕΥΤΙΚΟΥΣ ΚΑΙ ΔΙΑΤΡΟΦΙΚΟΥΣ ΠΑΡΑΓΟΝΤΕΣ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 19(Ι), 1-8.
  217. ΜΠΟΥΖΑ Ε., ΑΝΤΩΝΙΑΔΟΥ Ι., ΑΝΤΩΝΟΠΟΥΛΟΥ Ε., ΑΝΑΓΝΩΣΤΑΚΟΥ Μ., ΑΝΑΤΟΛΙΤΟΥ Φ., ΜΟΡΟΖΙΝΗ Μ., ΣΑΡΑΦΙΔΟΥ Γ., ΞΑΝΘΟΥ Μ. (2007) ΝΕΥΡΟΑΝΑΠΤΥΞΙΑΚΗ ΕΞΕΛΙΞΗ ΠΟΛΥ ΧΑΜΗΛΟΥ ΒΑΡΟΥΣ ΓΕΝΝΗΣΗΣ ΝΕΟΓΝΩΝ ΣΤΗΝ ΠΡΟΣΧΟΛΙΚΗ ΗΛΙΚΙΑ. ΠΑΙΔΙΑΤΡΙΚΗ. 70(2), 115-122.
  218. ΝΙΚΟΛΑΙΔΗΣ Γ. ΣΤΑΥΡΙΑΝΑΚΗ Μ. (2010) ΣΥΓΧΡΟΝΕΣ ΑΝΤΙΛΗΨΕΙΣ ΓΙΑ ΤΙΣ ΔΟΜΕΣ ΠΑΙΔΙΚΗΣ ΠΡΟΣΤΑΣΙΑΣ ΚΑΙ ΤΙΣ ΠΟΛΙΤΙΚΕΣ ΑΠΟΙΔΡΥΜΑΤΟΠΟΙΗΣΗΣ. ΚΟΙΝΩΝΙΚΗ ΕΡΓΑΣΙΑ. 100, 183-205.
  219. ΝΙΚΟΛΑΙΔΗΣ Γ. (2007) ΑΝΤΙΦΑΣΕΙΣ ΚΑΙ ΑΔΙΕΞΟΔΑ ΤΗΣ ΜΕΘΟΔΟΛΟΓΙΑΣ ΤΟΥ MANAGEMENT CARE: Η ΠΕΡΙΠΤΩΣΗ ΤΗΣ ΕΛΛΗΝΙΚΗΣ ΨΥΧΙΑΤΡΙΚΗΣ ΜΕΤΑΡΡΥΘΜΙΣΗΣ. ΚΟΙΝΩΝΙΑ, ΟΙΚΟΝΟΜΙΑ ΚΑΙ ΥΓΕΙΑ. 5(1), 68-91.
  220. ΝΙΚΟΛΑΙΔΗΣ Γ. (2007) ΟΡΘΟΛΟΓΙΣΜΟΣ ΚΑΙ ΘΕΩΡΗΤΙΚΕΣ ΠΡΟΣΕΓΓΙΣΕΙΣ ΤΩΝ ΣΥΝΑΙΣΘΗΜΑΤΩΝ. ΣΥΝΑΨΙΣ. 5 (ΑΝΟΙΞΗ 07), 52-64.
  221. ΝΙΚΟΛΑΙΔΗΣ Γ., ΠΕΤΡΟΥΛΑΚΗ Κ., ΣΤΑΥΡΙΑΝΑΚΗ Μ. (2008) ΜΕΘΟΔΟΛΟΓΙΚΗ ΠΕΡΙΓΡΑΦΗ ΕΡΕΥΝΑΣ ΓΙΑ ΤΗ ΜΕΛΕΤΗ ΤΗΣ ΕΚΤΑΣΗΣ ΚΑΙ ΤΩΝ ΧΑΡΑΚΤΗΡΙΣΤΙΚΩΝ ΤΗΣ ΒΙΑΣ ΚΑΤΑ ΑΝΗΛΙΚΩΝ, ΣΕ ΜΑΘΗΤΕΣ/ΤΡΙΕΣ Α' ΓΥΜΝΑΣΙΟΥ ΤΩΝ ΠΕΡΙΦΕΡΕΙΩΝ Β. ΚΑΙ Ν. ΑΙΓΑΙΟΥ. ΝΕΟΙ, ΕΓΚΛΗΜΑ ΚΑΙ ΚΟΙΝΩΝΙΑ. 1, 41-54.
  222. ΞΕΚΑΛΑΚΗ Α. ΑΝΤΩΝΙΑΔΟΥ-ΚΟΥΜΑΤΟΥ Ι. (2006) Η ΣΗΜΑΣΙΑ ΤΟΥ ΕΛΕΓΧΟΥ ΤΗΣ ΟΡΑΣΗΣ ΣΤΗΝ ΠΡΟΣΧΟΛΙΚΗ ΚΑΙ ΣΧΟΛΙΚΗ ΗΛΙΚΙΑ ΣΤΟ ΠΡΩΤΟΒΑΘΜΙΟ ΠΑΙΔΙΑΤΡΙΚΟ ΙΑΤΡΕΙΟ. ΠΑΙΔΙΑΤΡΙΚΗ. 69, 59-64.
  223. ΞΕΚΑΛΑΚΗ Α., ΜΕΝΕΓΑΣ Δ., ΖΟΛΩΤΑ Α., ΗΛΙΟΔΡΟΜΙΤΗ Ζ., ΠΡΑΣΟΥΛΗ Α., ΤΖΙΝΗ Ε., ΜΑΥΡΙΚΑ Π., ΔΗΜΟΠΟΥΛΟΥ Α., ΜΑΡΓΑΡΗ Α., ΑΝΤΩΝΙΑΔΟΥ Ι. (2008) ΠΡΟΤΥΠΟ ΠΡΟΓΡΑΜΜΑ ΑΓΩΓΗΣ ΚΑΙ ΠΡΟΑΓΩΓΗΣ ΥΓΕΙΑΣ ΣΕ ΑΣΤΙΚΗ ΚΟΙΝΟΤΗΤΑ ΑΠΟ ΦΟΡΕΑ ΠΡΩΤΟΒΑΘΜΙΑΣ ΦΡΟΝΤΙΔΑΣ ΥΓΕΙΑΣ. ΠΑΙΔΙΑΤΡΙΚΗ. 71, 469-474.
  224. ΠΑΠΑΦΥΛΑΚΤΟΥ Μ., ΛΑΠΑΤΣΑΝΗΣ Π., ΠΟΥΛΟΠΟΥΛΟΣ Π., PETERSEN M., ΜΙΧΑΛΑΚΑΚΟΥ Κ., ΠΡΟΥΝΤΖΟΥ-ΚΑΣΣΙΟΥ Κ. (2006) ΑΝΤΙΜΕΤΩΠΙΣΗ ΤΗΣ ΟΣΤΕΟΠΟΡΩΣΗΣ ΚΑΙ ΤΩΝ ΚΑΤΑΓΜΑΤΩΝ ΜΕ ΔΙΝΑΤΡΙΟΥΧΟ ΠΑΜΙΔΡΟΝΑΤΗ ΣΕ ΒΡΕΦΟΣ ΜΕ ΑΤΕΛΗ ΟΣΤΕΟΓΕΝΕΣΗ ΤΥΠΟΥ IV. ΠΑΙΔΙΑΤΡΙΚΗ. 69(6), 452-457.
  225. ΠΑΡΘΥΜΟΣ Θ., ΣΟΥΛΠΗ Κ., ΑΓΓΕΛΟΓΙΑΝΝΗ Π., ΚΑΡΙΚΑΣ Γ., ΠΑΡΘΥΜΟΣ Ν., ΤΣΑΚΙΡΗΣ Σ. (2008) Η ΧΟΡΗΓΗΣΗ L-ΚΥΣΤΕΙΝΗΣ ΑΠΟΤΡΕΠΕΙ ΤΙΣ ΠΡΟΚΛΗΘΕΙΣΕΣ ΜΕΤΑΒΟΛΕΣ ΑΠΟ ΤΗΝ ΑΣΚΗΣΗ ΣΤΙΣ ΔΡΑΣΤΙΚΟΤΗΤΕΣ ΑΚΕΤΥΛΟΧΟΛΙΝΕΣΤΕΡΑΣΗΣ ΚΑΙ NA+, K+ -ATPασης ΤΩΝ ΕΡΥΘΡΟΚΥΤΤΑΡΙΚΩΝ ΜΕΜΒΡΑΝΩΝ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 21 (ΙΙ), 63-72.
  226. ΠΕΤΡΟΥ Ζ., HEWITT A., SAMPLES J., MACKEY D., WIRT M., PETERSEN M.B., ΚΙΤΣΟΣ Γ. (2007) ΙΔΡΥΤΙΚΗ ΜΕΤΑΛΛΑΓΗ Thr377MET ΤΗΣ ΜΥΟΣΙΛΙΝΗΣ ΣΕ ΕΝΝΕΑ ΟΙΚΟΓΕΝΕΙΕΣ ΜΕ ΠΡΩΤΟΠΑΘΕΣ ΓΛΑΥΚΩΜΑ ΑΝΟΙΚΤΗΣ ΓΩΝΙΑΣ ΜΕ ΔΙΑΦΟΡΕΤΙΚΗ ΜΕΤΑΞΥ ΤΟΥΣ ΕΘΝΙΚΗ ΚΑΤΑΓΩΓΗ. ΟΦΘΑΛΜΟΛΟΓΙΚΑ ΧΡΟΝΙΚΑ. 17(3), 289-294.
  227. ΠΡΑΣΟΥΛΗ Α., ΑΤΤΙΛΑΚΟΣ Α., ΑΝΤΩΝΙΑΔΟΥ Ι. (2008) Η ΕΠΙΔΡΑΣΗ ΤΗΣ ΠΑΙΔΙΚΗΣ ΕΠΙΛΗΨΙΑΣ ΣΤΙΣ ΓΝΩΣΤΙΚΕΣ ΛΕΙΤΟΥΡΓΙΕΣ ΚΑΙ ΣΤΗ ΣΥΜΠΕΡΙΦΟΡΑ. ΠΑΙΔΙΑΤΡΙΚΗ. 71(6), 426-433.
  228. ΣΟΥΛΠΗ Κ., ΓΑΒΡΙΛΗ Σ., ΚΑΡΑΚΩΝΣΤΑΝΤΑΚΗΣ Θ., ΚΑΡΙΚΑΣ Γ., ΒΛΑΧΟΣ Γ., ΚΩΣΤΑΛΟΣ Χ., ΠΑΠΑΣΩΤΗΡΙΟΥ Ι. (2006) ΕΠΙΠΕΔΑ ΣΕΛΗΝΙΟΥ ΚΑΙ ΧΑΛΚΟΥ ΑΙΜΑΤΟΣ ΜΗΤΕΡΩΝ ΚΑΙ ΝΕΟΓΝΩΝ ΕΛΛΗΝΙΚΗΣ ΚΑΙ ΑΛΒΑΝΙΚΗΣ ΚΑΤΑΓΩΓΗΣ. ΠΑΙΔΙΑΤΡΙΚΗ. 69, 199-204.
  229. ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΠΑΡΘΥΜΟΣ Θ., ΤΣΑΚΙΡΗΣ Θ., ΠΑΡΘΥΜΟΣ Ν., ΤΣΑΚΙΡΗΣ Σ. (2008) Η ΕΠΙΔΡΑΣΗ ΤΗΣ ΠΡΟΠΟΝΗΣΗΣ ΥΨΗΛΗΣ ΕΝΤΑΣΗΣ ΣΤΑ ΕΠΙΠΕΔΑ ΤΗΣ ΝΕΥΡΟΠΡΩΤΕΙΝΗΣ S100B ΣΤΟΝ ΟΡΟ ΑΘΛΗΤΩΝ ΚΑΛΑΘΟΣΦΑΙΡΙΣΗΣ. Ο ΡΟΛΟΣ ΤΗΣ ΧΟΡΗΓΗΣΗΣ α-ΤΟΚΟΦΕΡΟΛΗΣ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 21(ΙΙΙ), 82-92.
  230. ΣΟΥΛΠΗ Κ., ΚΑΡΙΚΑΣ Γ., ΡΕΚΛΟΣ Γ., ΠΑΡΘΥΜΟΣ Θ., ΠΑΡΘΥΜΟΣ Ν., ΓΑΒΡΙΗΛΙΔΗΣ Α., ΤΣΑΚΙΡΗΣ Σ. (2008) Η ΧΟΡΗΓΗΣΗ ΤΗΣ L-ΚΥΣΤΕΙΝΗΣ ΠΡΟΣΤΑΤΕΥΕΙ ΤΗ ΔΡΑΣΤΙΚΟΤΗΤΑ ΤΗΣ ΓΛΥΚΟΖΟ-6-ΦΩΣΦΟΡΙΚΗΣ-ΔΕΥΔΡΟΓΕΝΑΣΗΣ ΤΩΝ ΕΡΥΘΡΟΚΥΤΤΑΡΩΝ ΑΘΛΗΤΩΝ ΑΠΟ ΤΗ ΜΕΙΩΣΗ ΠΟΥ ΕΠΑΓΕΤΑΙ ΑΠΟ ΠΡΟΠΟΝΗΣΗ ΥΨΗΛΗΣ ΕΝΤΑΣΗΣ ΚΑΙ ΤΗΝ ΠΑΡΑΓΩΓΗ ΕΛΕΥΘΕΡΩΝ ΡΙΖΩΝ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 21(ΙΙΙ), 91-98.
  231. ΣΟΦΙΑΝΟΥΑ. (2007) NATURAL HISTORY OF PHYSICAL URTICARIA IN CHILDREN. EUROPEAN JOURNAL OF PAEDIATRIC ALLERGY AND IMMUNOLOGY. epub ahead of publishing.
  232. ΣΟΦΙΑΝΟΥ Α. (2007) ΟΙ ΑΛΛΕΡΓΙΚΕΣ ΠΑΘΗΣΕΙΣ ΣΤΗ ΣΥΓΧΡΟΝΗ ΕΠΟΧΗ: Η ΕΠΙΔΗΜΙΟΛΟΓΙΑ ΚΑΙ ΑΥΞΗΤΙΚΕΣ ΤΑΣΕΙΣ. ΠΑΙΔΙΑΤΡΙΚΗ. 70(4), 266-271.
  233. ΣΤΑΥΡΙΑΝΑΚΗ Μ. (2005) ΑΝΑΔΟΧΗ ΦΡΟΝΤΙΔΑ ΚΑΙ ΔΙΚΑΙΩΜΑΤΑ ΠΑΙΔΙΩΝ: ΑΝΤΙΣΤΟΙΧΙΕΣ ΚΑΙ ΑΝΤΙΦΑΣΕΙΣ. ΚΟΙΝΩΝΙΚΗ ΕΡΓΑΣΙΑ. 80, 195-205.
  234. ΣΤΑΥΡΙΑΝΑΚΗ Μ., ΚΥΡΙΑΚΟΠΟΥΛΟΥ Α., ΡΙΓΚΑ Α., ΝΙΚΟΛΑΙΔΗΣ Γ. (2008) ΜΕΘΟΔΟΛΟΓΙΑ DELPHI: ΜΙΑ ΠΟΙΟΤΙΚΗ ΠΡΟΣΕΓΓΙΣΗ ΤΟΥ ΦΑΙΝΟΜΕΝΟΥ ΤΗΣ ΒΙΑΣ ΚΑΤΑ ΑΝΗΛΙΚΩΝ. ΚΟΙΝΩΝΙΚΗ ΕΡΓΑΣΙΑ. ΕΤΟΣ 23ο (89), 7-28.
  235. ΤΣΑΚΙΡΗΣ Σ., ΚΑΡΙΚΑΣ Γ., ΠΑΡΘΥΜΟΣ Θ., ΠΑΡΘΥΜΟΣ Ν., ΤΣΑΚΙΡΗΣ Θ., ΣΟΥΛΠΗ Κ. (2009) Η ΧΟΡΗΓΗΣΗ α-ΤΟΚΟΦΕΡΟΛΗΣ ΠΡΟΣΤΑΤΕΥΕΙ ΤΙΣ ΔΡΑΣΤΙΚΟΤΗΤΕΣ ΤΩΝ ΕΝΖΥΜΩΝ ΠΑΡΑΟΞΑΝΑΣΗ 1/ΑΡΥΛΕΣΤΕΡΑΣΗ ΤΟΥ ΟΡΟΥ ΑΠΟ ΕΛΑΤΤΩΣΗ ΠΡΟΚΑΛΟΥΜΕΝΗ ΑΠΟ ΤΗΝ ΠΡΟΠΟΝΗΣΗ ΥΨΗΛΗΣ ΕΝΤΑΣΗΣ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 22, III, 97-105.
  236. ΤΣΑΚΙΡΗΣ Σ., ΚΑΡΙΚΑΣ Γ., ΠΑΡΘΥΜΟΣ Θ., ΠΑΡΘΥΜΟΣ Ν., ΤΣΑΚΙΡΗΣ Θ., ΣΟΥΛΠΗ Κ. (2009) Η ΧΟΡΗΓΗΣΗ α-ΤΟΚΟΦΕΡΟΛΗΣ ΠΡΟΣΤΑΤΕΥΕΙ ΤΙΣ ΔΡΑΣΤΙΚΟΤΗΤΕΣ ΤΩΝ ΕΝΖΥΜΩΝ ΠΑΡΑΟΞΑΝΑΣΗ 1/ΑΡΥΛΕΣΤΕΡΑΣΗ ΤΟΥ ΟΡΟΥ ΑΠΟ ΕΛΑΤΤΩΣΗ ΠΡΟΚΑΛΟΥΜΕΝΗ ΑΠΟ ΤΗΝ ΠΡΟΠΟΝΗΣΗ ΥΨΗΛΗΣ ΕΝΤΑΣΗΣ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 22 III, 97-105.
  237. ΤΣΑΚΙΡΗΣ Σ., ΠΑΡΘΥΜΟΣ Θ., ΡΕΚΛΟΣ Γ., ΚΑΡΙΚΑΣ Γ., ΠΑΡΘΥΜΟΣ Ν., ΤΣΑΚΙΡΗΣ Θ., ΣΟΥΛΠΗ Κ. (2009) ΜΕΙΩΣΗ ΤΗΣ ΔΡΑΣΤΙΚΟΤΗΤΑΣ ΤΗΣ ΕΡΥΘΡΟΚΥΤΤΑΡΙΚΗΣ ΓΛΥΚΟΖΟ-6-ΦΩΣΦΟΡΙΚΗΣ ΔΕΥΔΡΟΓΕΝΑΣΗΣ ΣΕ ΠΟΔΟΣΦΑΙΡΙΣΤΕΣ ΚΑΤΑ ΤΗ ΔΙΑΡΚΕΙΑ ΤΟΥ ΠΑΙΧΝΙΔΙΟΥ. ΣΤΟΙΧΕΙΑ ΕΠΙΔΡΑΣΗΣ ΤΟΥ ΝΕΥΡΟΕΝΔΟΚΡΙΝΙΚΟΥ ΣΥΣΤΗΜΑΤΟΣ ΣΤΗΝ ΕΝΖΥΜΙΚΗ ΔΡΑΣΤΙΚΟΤΗΤΑ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 22(II), 62-70.
  238. ΤΣΑΚΙΡΗΣ Σ., ΣΟΥΛΠΗ Κ., ΓΚΡΟΥΖΜΑΝ Ε., ΖΛΑΤΙΝΟΥΔΗΣ Χ., ΤΣΙΡΙΒΑ Μ., ΚΑΡΙΚΑΣ Γ. (2007) Ο ΠΡΟΣΤΑΤΕΥΤΙΚΟΣ ΡΟΛΟΣ ΤΩΝ Ω-3 ΚΑΙ Ω-6 ΛΙΠΑΡΩΝ ΟΞΕΩΝ ΣΤΙΣ ΕΓΚΕΦΑΛΙΚΕΣ ΛΕΙΤΟΥΡΓΙΕΣ. ΦΑΡΜΑΚΕΥΤΙΚΗ. 20 ΙΙ, 56-67.