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Showing articles 0 to 8 of 8 Filter Applied: metabolic disorder,primary (Click to remove) Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Inherited Metabolic Diseases of the Nervous System, Pyridoxine Dependent Seizures Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014 Conditions That Mimic Stroke in the Emergency Department Arch Neurol 52:1119-1122, Libman,R.B.,et al, 1995 Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989 Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin NEJM 304:817-820, Thoene,J.,et al, 1981 Abnormality of a Thiamine-Requiring Enzyme in Patients with Wernicke-Korsakoff Syndrome NEJM 297:1367, Blass,J.P.,et al, 1977 Inherited Aminoacidopathies Demonstrating Vitamin Dependency NEJM 281:145, Rosenberg,L., 1965 Angiokeratoma Corporis Diffusum Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962 Showing articles 0 to 8 of 8