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.
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125. 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.
126. 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.
127. 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.
128. 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.
129. 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.
130. 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.
131. 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.
132. 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.
133. 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.
134. 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.
135. 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.
136. 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.
137. 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.
138. 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.
139. 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.
140. 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.
141. 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.
142. 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.
143. 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.
144. 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.
145. 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.
146. 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.
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149. 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.
150. 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.
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152. 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.
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