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The Journal of Pediatrics|January 1, 1992
Enzymatic diagnosis of nonketotic hyperglycinemia with lymphoblastsS Kure, K Narisawa, K TadaEnzyme|January 1, 1987
Glycogen storage disease type 1b: genetic disorder involving the transport system of intracellular membraneK Narisawa, Y Igarashi, K TadaEuropean Journal of Pediatrics|March 1, 1992
Medium-chain acyl-CoA dehydrogenase deficiency: molecular aspectsY Matsubara, K Narisawa, K TadaThe Japanese Journal of Human Genetics|March 1, 1997
Nonketotic hyperglycinemia: biochemical, molecular, and neurological aspectsS Kure, K Tada, K NarisawaBiochemical and Biophysical Research Communications|February 14, 1991
Structural and expression analyses of normal and mutant mRNA encoding glycine decarboxylase: three-base deletion in mRNA causes nonketotic hyperglycinemiaS Kure, K Narisawa, K TadaBiochemical Medicine|April 1, 1985
Glycogen storage disease type IB: a new model of genetic disorders involving the transport system of intracellular membraneK Tada, K Narisawa, Y Igarashi, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|October 16, 1989
Assay of methylmalonyl CoA mutase with high-performance liquid chromatographyM Kikuchi, H Hanamizu, K Narisawa, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1990
Enzymatic diagnosis of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency with high-performance liquid chromatographyM Kikuchi, K Narisawa, K Tada, et al.The Tohoku Journal of Experimental Medicine|October 1, 1979
A lymphoblastoid cell line from an adenosine deaminase deficient patient established by Epstein-Barr virusS Tsuchiya, K Narisawa, T Konno, et al.Journal of Nutritional Science and Vitaminology|January 1, 1992
Thiamine responsive pyruvate dehydrogenase deficiencyK Narisawa, H Endo, S Miyabayashi, et al.Pageof 52