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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 13, 2012
Heritable disorders in the metabolism of the dolichols: A bridge from sterol biosynthesis to molecular glycosylationLynne A Wolfe, Eva Morava, Miao He, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 10, 2018
A proposed nosology of inborn errors of metabolismCarlos R Ferreira, Clara D M van Karnebeek, Jerry Vockley, et al.
Molecular Genetics and Metabolism|September 15, 2020
Effects of fasting, feeding and exercise on plasma acylcarnitines among subjects with CPT2D, VLCADD and LCHADD/TFPDGabriela Elizondo, Dietrich Matern, Jerry Vockley, et al.
Molecular Genetics and Metabolism|May 22, 2021
Successful orthotopic heart transplantation in CPTII deficiencyGeorgianne L Arnold, Jessie Yester, Elizabeth McCracken, et al.
Biochimica Et Biophysica Acta|September 1, 2004
Thermal unfolding of medium-chain acyl-CoA dehydrogenase and iso(3)valeryl-CoA dehydrogenase: study of the effect of genetic defects on enzyme stabilityIbrahim Nasser, Al-Walid Mohsen, Ilian Jelesarov, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 24, 2020
Living Related Liver Transplantation for Metabolic Liver Diseases in ChildrenVikrant Sood, James E Squires, George V Mazariegos, et al.
Molecular Genetics and Metabolism|April 5, 2022
Phenylketonuria oxidative stress and energy dysregulation: Emerging pathophysiological elements provide interventional opportunitySteven F Dobrowolski, Yu Leng Phua, Jerry Vockley, et al.
Molecular Genetics and Metabolism|August 5, 2019
Perspectives on urea cycle disorder management: Results of a clinician surveyGregory M Enns, Marty H Porter, Megan Francis-Sedlak, et al.
Molecular Genetics and Metabolism|March 14, 2013
Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiencyManuel Schiff, Al-Walid Mohsen, Anuradha Karunanidhi, et al.
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