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Proceedings of the National Academy of Sciences of the United States of America|September 15, 1992
Molecular characterization of inherited carnitine palmitoyltransferase II deficiencyF Taroni, E Verderio, S Fiorucci, et al.Human Molecular Genetics|January 1, 1995
Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutationsE Verderio, P Cavadini, L Montermini, et al.Neuromuscular Disorders : NMD|May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuriaC Minetti, B Garavaglia, M Bado, et al.Journal of Inherited Metabolic Disease|September 3, 1999
Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: insights on treatmentR Parini, F Invernizzi, F Menni, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2001
Phenotype and genotype variation in primary carnitine deficiencyY Wang, S H Korman, J Ye, et al.Gastroenterology|September 1, 1995
The risk of adenomatous polyps in asymptomatic first-degree relatives of persons with colon cancerF Bazzoli, S Fossi, S Sottili, et al.Neuroreport|November 1, 1990
Locomotor projections from the pedunculopontine nucleus to the medioventral medullaR D Skinner, N Kinjo, Y Ishikawa, et al.American Journal of Human Genetics|May 1, 1996
Molecular analysis of carnitine palmitoyltransferase II deficiency with hepatocardiomuscular expressionJ P Bonnefont, F Taroni, P Cavadini, et al.Annals of Allergy|December 1, 1989
Once versus twice daily dosing of terfenadine in the treatment of seasonal allergic rhinitis: US and European studiesT J Chu, M Yamate, A A Biedermann, et al.Brain Research. Developmental Brain Research|June 21, 1991
Fibroblast growth factor-induced increased survival of cholinergic mesopontine neurons in cultureE Garcia-Rill, D L Davies, R D Skinner, et al.Pageof 17