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Journal of Inherited Metabolic Disease|January 1, 1994
Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one alleleN Gregersen, V Winter, S Lyonnet, et al.Stroke|June 17, 2025
Compensatory Proximal Adjustments Characterize Effective Reaching Movements After StrokeSilke Wolf, Leoni V Winter, Naveen Elangovan, et al.The Journal of Biological Chemistry|April 28, 1995
Effects of two mutations detected in medium chain acyl-CoA dehydrogenase (MCAD)-deficient patients on folding, oligomer assembly, and stability of MCAD enzymeP Bross, C Jespersen, T G Jensen, et al.Prenatal Diagnosis|January 1, 1995
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhoodN Gregersen, V Winter, P K Jensen, et al.Movement Ecology|May 30, 2026
Upstream passage windows for anadromous fish at a large barrier in the Rhine-Meuse estuary, 1996-2018Melanie P Meijer Zu Schlochtern, Leopold A J Nagelkerke, Anthonie D Buijse, et al.Deutsche Medizinische Wochenschrift (1946)|October 21, 2016
[Decompensated right heart failure, intensive care and perioperative management in patients with pulmonary hypertension]K M Olsson, M Halank, B Egenlauf, et al.Schmerz (Berlin, Germany)|June 30, 2017
[What does pain intensity mean from the patient perspective? : A qualitative study on the patient perspective of pain intensity as an outcome parameter in treatment evaluation and on the interpretability of pain intensity measurements]K Neustadt, S Deckert, C Kopkow, et al.American Journal of Human Genetics|September 1, 1993
A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)B S Andresen, P Bross, T G Jensen, et al.Human Genetics|August 1, 1991
The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the geneS Kølvraa, N Gregersen, A I Blakemore, et al.American Journal of Physiology. Endocrinology and Metabolism|May 16, 2026
Alterations in glucocorticoid homeostasis following sleeve gastrectomy in male miceSeraina O Moser, Andrei Moscalu, Cullen F Roberts, et al.Pageof 16