C. Prasad

Update on transcobalamin deficiency: clinical presentation, treatment and outcome

Yannis Trakadis, Ahmed Alfares, Olaf A. Bodamer et al. · Journal of Inherited Metabolic Disease · 2013 · 78 citations

Outcome of the First 3-Years of a DNA-Based Neonatal Screening Program for Glutaric Acidemia Type 1 in Manitoba and Northwestern Ontario, Canada

Cheryl R. Greenberg, Asuri N. Prasad, Louise A. Dilling et al. · Molecular Genetics and Metabolism · 2002 · 78 citations

Newborn Screening, Neonatology, First 3-Years +6

Hepatic Carnitine Palmitoyl Transferase 1 (CPT1 A) Deficiency in North American Hutterites (Canadian and American): Evidence for a Founder Effect and Results of a Pilot Study on a DNA-Based Newborn Screening Program

C. Prasad, John P. Johnson, Jean‐Paul Bonnefont et al. · Molecular Genetics and Metabolism · 2001 · 50 citations

Genetic Testing, Hepatology, Cpt1 A +9

Mutations of the E1β subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiency

K Okajima, Lioubov G. Korotchkina, C. Prasad et al. · Molecular Genetics and Metabolism · 2008 · 48 citations

E1β Subunit Gene, Aldehyde Dehydrogenase, Biochemistry +9

Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features

AJ Dawson, Sydney Putnam, Jack C. Schultz et al. · Clinical Genetics · 2002 · 47 citations