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B Melegh

Showing results (21-30 of 99) with videos related to

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Acta Paediatrica Hungarica|January 1, 1990
Feeding preterm infants with L-carnitine supplemented formulaB Melegh, J Kerner, L Szücs, et al.
Orvosi Hetilap|February 27, 1994
[Carnitine-deficient cardiomyopathy]K Kádár, B Melegh, E Szendrei, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1990
Cytochrome oxidase deficiency affecting the structure of the myofibre and the shape of mitochondrial cristae membraneB Sumegi, B Melegh, K Adamovich, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1988
Changes of plasma free amino acids and renal clearances of carnitines in premature infants during L-carnitine-supplemented human milk feedingB Melegh, L Szücs, J Kerner, et al.
Clinical Genetics|January 5, 2001
Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian childrenE Morava, M Czakó, B Melegh, et al.
Acta Paediatrica Hungarica|January 1, 1986
Uptake of beta-hydroxybutyrate, acetoacetate and glucose by the forearm of the newborn infantB Melegh, J Kerner, M Vincellér, et al.
Biochimica Et Biophysica Acta|June 14, 1985
Release of carnitine from the perfused rat liverA Sandor, G Kispal, B Melegh, et al.
American Journal of Medical Genetics|October 2, 1996
Multiple mitochondrial DNA deletions and persistent hyperthermia in a patient with Brachmann-de Lange phenotypeB Melegh, I Bock, I Gáti, et al.
Biochimica Et Biophysica Acta|January 9, 1987
Enhanced uptake of carnitine by perfused rat liver following starvationG Kispal, B Melegh, I Alkonyi, et al.
European Journal of Pediatrics|September 4, 1998
Umbilical venous catheterization and development of Banti syndrome: the possible role of the factor V Leiden mutationJ Stankovics, A Nagy, K Méhes, et al.
Pageof 10

Showing results (21-30 of 99) with videos related to

Sort By:
Pageof 10
Acta Paediatrica Hungarica|January 1, 1990
Feeding preterm infants with L-carnitine supplemented formulaB Melegh, J Kerner, L Szücs, et al.
Orvosi Hetilap|February 27, 1994
[Carnitine-deficient cardiomyopathy]K Kádár, B Melegh, E Szendrei, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1990
Cytochrome oxidase deficiency affecting the structure of the myofibre and the shape of mitochondrial cristae membraneB Sumegi, B Melegh, K Adamovich, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1988
Changes of plasma free amino acids and renal clearances of carnitines in premature infants during L-carnitine-supplemented human milk feedingB Melegh, L Szücs, J Kerner, et al.
Clinical Genetics|January 5, 2001
Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian childrenE Morava, M Czakó, B Melegh, et al.
Acta Paediatrica Hungarica|January 1, 1986
Uptake of beta-hydroxybutyrate, acetoacetate and glucose by the forearm of the newborn infantB Melegh, J Kerner, M Vincellér, et al.
Biochimica Et Biophysica Acta|June 14, 1985
Release of carnitine from the perfused rat liverA Sandor, G Kispal, B Melegh, et al.
American Journal of Medical Genetics|October 2, 1996
Multiple mitochondrial DNA deletions and persistent hyperthermia in a patient with Brachmann-de Lange phenotypeB Melegh, I Bock, I Gáti, et al.
Biochimica Et Biophysica Acta|January 9, 1987
Enhanced uptake of carnitine by perfused rat liver following starvationG Kispal, B Melegh, I Alkonyi, et al.
European Journal of Pediatrics|September 4, 1998
Umbilical venous catheterization and development of Banti syndrome: the possible role of the factor V Leiden mutationJ Stankovics, A Nagy, K Méhes, et al.
Pageof 10