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Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|July 1, 1990
Inherited disorders of vitamin B12 utilizationD S Rosenblatt, B A CooperSeminars in Hematology|February 4, 1999
Cobalamin and folate deficiency: acquired and hereditary disorders in childrenD S Rosenblatt, V M WhiteheadAdvances in Experimental Medicine and Biology|January 1, 1983
Methotrexate polyglutamates in cultured human cellsD S Rosenblatt, V M WhiteheadClinical and Investigative Medicine. Medecine Clinique Et Experimentale|August 1, 1992
Methionine auxotrophy in inborn errors of cobalamin metabolismV Garovic-Kocic, D S RosenblattBulletin De L'Academie Nationale De Medecine|October 1, 1996
[A molecular study of methylmalonic aciduria: structure-function correlations]D S Rosenblatt, F D LedleyThe Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1992
The neurology of cobalaminM I Shevell, D S RosenblattHuman Mutation|January 1, 1997
Mutations in mut methylmalonic acidemia: clinical and enzymatic correlationsF D Ledley, D S RosenblattAdvances in Experimental Medicine and Biology|January 1, 1983
Methotrexate metabolism by bone marrow cells from patients with leukemiaV M Whitehead, D S RosenblattHuman Molecular Genetics|December 1, 1996
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disordersD Leclerc, E Campeau, P Goyette, et al.Journal of Medical Genetics|July 7, 2000
Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH)D Watkins, N Matiaszuk, D S RosenblattPageof 140