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The New England Journal of Medicine|December 11, 1980
Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndromeP R Chapoy, C Angelini, W J Brown, et al.Somatic Cell and Molecular Genetics|November 1, 1996
Delivery of cytosolic liver arginase into the mitochondrial matrix space: a possible novel site for gene replacement therapyP B Wissmann, B K Goodman, J G Vockley, et al.Pediatrics|November 1, 1976
Ketonic diet in the management of pyruvate dehydrogenase deficiencyR E Falk, S D Cederbaum, J P Blass, et al.Pediatric Research|June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeN Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.Molecular Genetics and Metabolism|October 6, 1998
Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginaseD E Ash, L R Scolnick, Z F Kanyo, et al.Archives of Biochemistry and Biophysics|July 1, 1987
Regulation of mRNA levels for five urea cycle enzymes in rat liver by diet, cyclic AMP, and glucocorticoidsS M Morris, C L Moncman, K D Rand, et al.[Hokkaido Igaku Zasshi] the Hokkaido Journal of Medical Science|April 18, 1998
[The importance of informed consent in the field of ophthalmology]A YoshidaIsozymes|January 1, 1983
Differences in the isozymes involved in alcohol metabolism between caucasians and orientalsA YoshidaHuman Genetics|January 1, 1984
Determination of aldehyde dehydrogenase phenotypes using hair roots: re-examinationA YoshidaPageof 137