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Results: 1-11 |
Results: 11
Carnitine-responsive carnitine insufficiency in a case of mtDNA 8993T > C mutation associated Leigh syndrome
Authors: Toth, G Morava, E Bene, J Selhorst, JJM Overmars, H Vreken, P Molnar, J Farkas, V Melegh, B
Citation: G. Toth et al., Carnitine-responsive carnitine insufficiency in a case of mtDNA 8993T > C mutation associated Leigh syndrome, J INH MET D, 24(3), 2001, pp. 421-422
Hyperhomocysteinaemia and MTHFR C677T gene polymorphism in renal transplant recipients
Authors: Szabo, AJ Tulassay, T Melegh, B Szabo, T Szabo, A Vannay, A Fekete, A Suveges, Z Reusz, GS
Citation: Aj. Szabo et al., Hyperhomocysteinaemia and MTHFR C677T gene polymorphism in renal transplant recipients, ARCH DIS CH, 85(1), 2001, pp. 47-49
Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian children
Authors: Morava, E Czako, M Melegh, B Kosztolanyi, G
Citation: E. Morava et al., Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian children, CLIN GENET, 58(5), 2000, pp. 403-405
High prevalence of factor V Leiden mutation in mothers of premature neonates
Authors: Erhardt, E Stankovics, J Molnar, D Adamovich, K Melegh, B
Citation: E. Erhardt et al., High prevalence of factor V Leiden mutation in mothers of premature neonates, BIOL NEONAT, 78(2), 2000, pp. 145-146
Urinary glycosaminoglycan excretion in urolithiasis
Authors: Harangi, F Gyorke, Z Melegh, B
Citation: F. Harangi et al., Urinary glycosaminoglycan excretion in urolithiasis, ARCH DIS CH, 82(1), 2000, pp. 89-90
Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies
Authors: Herczegfalvi, A Toth, G Gyurus, P Morava, E Endreffy, E Fodor, F Mechler, F Laszlo, A Rasko, I Melegh, B
Citation: A. Herczegfalvi et al., Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies, NEUROMUSC D, 9(8), 1999, pp. 552-554
Cefetamet pivoxil treatment causes loss of carnitine reserves that can be prevented by exogenous carnitine administration
Authors: Pap, M Kopcsanyi, G Bieber, LL Gage, DA Melegh, B
Citation: M. Pap et al., Cefetamet pivoxil treatment causes loss of carnitine reserves that can be prevented by exogenous carnitine administration, J NUTR BIOC, 10(11), 1999, pp. 670-673
Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population
Authors: Gyurus, P Molnar, J Melegh, B Toth, G Morava, E Kosztolanyi, G Mehes, K
Citation: P. Gyurus et al., Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population, AM J MED G, 87(3), 1999, pp. 245-250
Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy
Authors: Melegh, B Seress, L Bedekovics, T Kispal, G Sumegi, B Trombitas, K Mehes, K
Citation: B. Melegh et al., Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy, J INH MET D, 22(7), 1999, pp. 827-838
Labeled trimethyllysine load depletes unlabeled carnitine in premature infants without evidence of incorporation
Authors: Melegh, B Toth, G Adamovich, K Szekely, G Gage, DA Bieber, LL
Citation: B. Melegh et al., Labeled trimethyllysine load depletes unlabeled carnitine in premature infants without evidence of incorporation, BIOL NEONAT, 76(1), 1999, pp. 19-25
Homoplastic A12,753G mitochondrial DNA mutation in a Hungarian family
Authors: Kis, A Matolcsy, A Vecsei, L Kosztolanyi, G Mehes, K Melegh, B
Citation: A. Kis et al., Homoplastic A12,753G mitochondrial DNA mutation in a Hungarian family, ACT BIOL HU, 49(1), 1998, pp. 119-124
Risultati: 1-11 |