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The Journal of Pediatrics|March 1, 1990
3-Hydroxydicarboxylic aciduria--a fatty acid oxidation defect with severe prognosisL Hagenfeldt, U von Döbeln, E Holme, et al.Lancet (London, England)|August 26, 1989
Carnitine deficiency induced by pivampicillin and pivmecillinam therapyE Holme, J Greter, C E Jacobson, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1993
Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenaseT C Gibbs, J Payan, E M Brett, et al.British Heart Journal|December 1, 1995
Transient reduction of human left ventricular mass in carnitine depletion induced by antibiotics containing pivalic acidK Abrahamsson, M Mellander, B O Eriksson, et al.American Journal of Medical Genetics. Part A|June 6, 2024
A novel homozygous pathogenic missense variant in COX6B1: Further delineation of the phenotypeE Jennions, M Olsson-Engman, K Visuttijai, et al.Nature Genetics|March 21, 1998
Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in miceN G Larsson, J Wang, H Wilhelmsson, et al.Human Genetics|August 15, 2000
Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type IIIU Rüetschi, R Cerone, C Pérez-Cerda, et al.Clinical and Experimental Pharmacology & Physiology|April 1, 1995
Use of primary cultures and continuous cell lines to study effects on astrocytic regulatory functionsE Walum, G Eriksson, A Peterson, et al.European Heart Journal|August 24, 1999
Humoral and cellular immune responses up to 7.5 years after administration of streptokinase for acute myocardial infarctionI B Squire, W Lawley, S Fletcher, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
Hydroxylation of aspartic acid in domains homologous to the epidermal growth factor precursor is catalyzed by a 2-oxoglutarate-dependent dioxygenaseJ Stenflo, E Holme, S Lindstedt, et al.Pageof 22