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Clinical Nephrology|February 12, 2002
Enzyme replacement therapy for Fabry disease, an inherited nephropathyR J Desnick, M Banikazemi, M WassersteinDevelopmental Neuroscience|January 1, 1995
Pre- and postnatal effects of chronic maternal hypoxia on substance-P immunoreactivity in rabbit brainstem regionsJ L Gingras, W A Long, T Segreti, et al.Molecular Genetics and Metabolism|March 1, 2015
Newborn screening for X-linked adrenoleukodystrophy in New York State: diagnostic protocol, surveillance protocol and treatment guidelinesB H Vogel, S E Bradley, D J Adams, et al.Journal of Inherited Metabolic Disease|December 23, 2006
Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiencyG S Salomons, C Jakobs, L Landegge Pope, et al.Pageof 1