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Journal of Inherited Metabolic Disease|January 1, 1982
The use of deuterated phenylalanine for the in vivo assay of phenylalanine hydroxylase activity in childrenR Matalon, D E Matthews, K Michals, et al.Pediatrics|April 1, 1983
Nonketotic hyperglycinemia: treatment with diazepam--a competitor for glycine receptorsR Matalon, S Naidu, J R Hughes, et al.Biochemical Medicine|August 1, 1983
Glucose-6-phosphatase as a marker for tumors of liver and kidney originK Michals, K Pringle, E J Pang, et al.Journal of the American Dietetic Association|October 1, 1988
Blood phenylalanine levels and intelligence of 10-year-old children with PKU in the National Collaborative StudyK Michals, C Azen, P Acosta, et al.Clinical Pediatrics|June 1, 1992
A treatment program for adolescents with phenylketonuriaL A Gleason, K Michals, R Matalon, et al.American Journal of Medical Genetics|February 1, 1988
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan diseaseR Matalon, K Michals, D Sebesta, et al.American Journal of Human Genetics|July 1, 1994
Canavan disease: mutations among Jewish and non-Jewish patientsR Kaul, G P Gao, M Aloya, et al.The Journal of Pediatrics|January 1, 1984
Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acidR Matalon, D A Stumpf, K Michals, et al.Neuroscience Letters|March 16, 2004
Mental retardation and hypotonia seen in the knock out mouse for Canavan disease is not due to succinate semialdehyde dehydrogenase deficiencyS Surendran, E L Ezell, M J Quast, et al.International Journal of Immunopathology and Pharmacology|September 17, 2005
Abnormal expression of genes associated with development and inflammation in the heart of mouse maternal phenylketonuria offspringR Matalon, S Surendran, J D McDonald, et al.Pageof 12