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Results: 1-16 |
Results: 16

Authors: LABADARIDIS J DIMITRIOU E COSTALOS C AERTS J VANWEELY S DONKERKOOPMAN WE MICHELAKAKIS H
Citation: J. Labadaridis et al., SERIAL CHITOTRIOSIDASE ACTIVITY ESTIMATIONS IN NEONATAL SYSTEMIC CANDIDIASIS, Acta paediatrica, 87(5), 1998, pp. 605-605

Authors: SCHULPIS KH PAPAKONSTANTINOU E MICHELAKAKIS H THEODORIDIS T PAPANDREOU U CONSTANTOPOULOS A
Citation: Kh. Schulpis et al., ELEVATED SERUM PROLACTIN CONCENTRATIONS IN PHENYLKETONURIC PATIENTS ON A LOOSE DIET, Clinical endocrinology, 48(1), 1998, pp. 99-101

Authors: MICHELAKAKIS H DIMITRIOU E GEORGAKIS H KARABATSOS F FRAGODIMITRI C SARAPHIDOU J PREMETIS E KARAGIORGALAGANA M
Citation: H. Michelakakis et al., IRON OVERLOAD AND URINARY LYSOSOMAL-ENZYME LEVELS IN BETA-THALASSEMIAMAJOR, European journal of pediatrics, 156(8), 1997, pp. 602-604

Authors: SCHULPIS K PAPAKONSTANTINOU ED MICHELAKAKIS H PODSKARBI T PATSOURAS A SHIN Y
Citation: K. Schulpis et al., SCREENING FOR GALACTOSEMIA IN GREECE, Paediatric and perinatal epidemiology, 11(4), 1997, pp. 436-440

Authors: GOLDENFUM SL YOUNG E MICHELAKAKIS H TSAGARAKIS S WINCHESTER B
Citation: Sl. Goldenfum et al., MUTATION ANALYSIS IN 20 PATIENTS WITH HUNTER-DISEASE, Human mutation, 7(1), 1996, pp. 76-78

Authors: MICHELAKAKIS H SPANOU C KONDYLI A DIMITRIOU E VANWEELY S HOLLAK CEM VANOERS MHJ AERTS JMFG
Citation: H. Michelakakis et al., PLASMA TUMOR NECROSIS FACTOR-A (TNF-A) LEVELS IN GAUCHER DISEASE, Biochimica et biophysica acta. Molecular basis of disease, 1317(3), 1996, pp. 219-222

Authors: SCHULPIS K PAPAKONSTANTINOU ED MICHELAKAKIS H BARGELIOTIS A SHIN Y
Citation: K. Schulpis et al., ANTIATHEROGENIC LIPID PROFILE IN GALACTOSAEMIC PATIENTS ON SOYBEAN DIETS, Journal of inherited metabolic disease, 19(1), 1996, pp. 91-92

Authors: MICHELAKAKIS H DIMITRIOU E VANWEELY S BOOT RG MAVRIDOU I VERHOEK M AERTS JMFG
Citation: H. Michelakakis et al., CHARACTERIZATION OF GLUCOCEREBROSIDASE IN GREEK GAUCHER DISEASE PATIENTS - MUTATION ANALYSIS AND BIOCHEMICAL-STUDIES, Journal of inherited metabolic disease, 18(5), 1995, pp. 609-615

Authors: MICHELAKAKIS H PAPADIMITRIOU A DIVARIS R MAVRIDOU I DIMITRIOU E
Citation: H. Michelakakis et al., PLASMA LYSOSOMAL-ENZYME LEVELS IN PATIENTS WITH MOTOR-NEURON DISEASE, Journal of inherited metabolic disease, 18(1), 1995, pp. 72-74

Authors: ANIKSTER Y SHAAG A CHRISTENSEN E GLUSTEIN JZ FOIS A MICHELAKAKIS H NIGRO F PRONICKA E RIBES A ZABOT MT
Citation: Y. Anikster et al., THE MOLECULAR-BASIS OF CANAVAN-DISEASE IN EUROPEAN NON-JEWISH PATIENTS, Pediatric research, 37(4), 1995, pp. 146-146

Authors: SHAAG A ANIKSTER Y CHRISTENSEN E GLUSTEIN JZ FOIS A MICHELAKAKIS H NIGRO F PRONICKA E RIBES A ZABOT MT ELPELEG ON
Citation: A. Shaag et al., THE MOLECULAR-BASIS OF ASPARTOACYLASE DEFICIENCY IN EUROPEAN NON-JEWISH PATIENTS, American journal of human genetics, 57(4), 1995, pp. 1315-1315

Authors: SHAAG A ANIKSTER Y CHRISTENSEN E GLUSTEIN JZ FOIS A MICHELAKAKIS H NIGRO F PRONICKA E RIBES A ZABOT MT ELPELEG ON
Citation: A. Shaag et al., THE MOLECULAR-BASIS OF CANAVAN (ASPARTOACYLASE DEFICIENCY) DISEASE INEUROPEAN NON-JEWISH PATIENTS, American journal of human genetics, 57(3), 1995, pp. 572-580

Authors: MICHELAKAKIS H DELIS D ANASTASIADOU V BARTSOCAS C
Citation: H. Michelakakis et al., INEFFECTIVENESS OF CAPTOPRIL IN REDUCING CYSTINE EXCRETION IN CYSTINURIC CHILDREN, Journal of inherited metabolic disease, 16(6), 1993, pp. 1042-1043

Authors: SCHULPIS KH MICHELAKAKIS H CHAROKOPOS E PAPAKONSTANTINOU E MESSARITAKIS J SHIN Y
Citation: Kh. Schulpis et al., UDP-GALACTOSE-4-EPIMERASE IN A BOY WITH A TRISOMY-21, Journal of inherited metabolic disease, 16(6), 1993, pp. 1059-1060

Authors: SCHULPIS KH PAPACONSTANTINOU ED KOIDOU A MICHELAKAKIS H TZAMOURANIS J PATSOURAS A SHIN Y
Citation: Kh. Schulpis et al., UDP GALACTOSE-4-EPIMERASE DEFICIENCY IN A 5.5-YEAR-OLD GIRL WITH UNILATERAL CATARACT, Journal of inherited metabolic disease, 16(5), 1993, pp. 903-904

Authors: DIVRY P JAKOBS C VIANEYSABAN C GIBSON KM MICHELAKAKIS H PAPADIMITRIOU A DIVARI R CHABROL B COURNELLE MA LIVET MO
Citation: P. Divry et al., L-2-HYDROXYGLUTARIC ACIDURIA - 2 FURTHER CASES, Journal of inherited metabolic disease, 16(3), 1993, pp. 505-507
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