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American Journal of Human Genetics|May 1, 1977
Maple syrup urine disease: branched-chain keto acid decarboxylation in fibroblasts as measured with amino acids and keto acidsJ Dancis, J Hutzler, R P CoxAmerican Journal of Human Genetics|May 1, 1979
Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminologyJ Dancis, J Hutzler, R P CoxPediatric Research|July 1, 1976
Multiple enzyme defects in familial hyperlysinemiaJ Dancis, J Hutzler, N C Woody, et al.American Journal of Human Genetics|May 1, 1986
The significance of hyperpipecolatemia in Zellweger syndromeJ Dancis, J HutzlerBiochimica Et Biophysica Acta|January 23, 1975
Lysine-ketoglutarate reductase in human tissuesJ Hutzler, J DancisClinica Chimica Acta; International Journal of Clinical Chemistry|March 1, 1983
The determination of pipecolic acid: method and results of hospital surveyJ Hutzler, J DancisComparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1982
Comparative rates of metabolism of pipecolic acid in several animal speciesJ Dancis, J HutzlerBiochimica Et Biophysica Acta|July 17, 1981
The metabolism of D- and L-pipecolic acid in the rabbit and ratJ Dancis, J HutzlerCanadian Medical Association Journal|August 18, 1973
Variant maple syrup urine disease in mother and daughterL A Zaleski, J Dancis, R P Cox, et al.Journal of Inherited Metabolic Disease|January 1, 1983
Hair root analysis in X-linked ichthyosisJ Dancis, V Jansen, J HutzlerPageof 17