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Journal of the American College of Nutrition|April 1, 1997
Phenylketonuria: current dietary treatment practices in the United States and CanadaR O Fisch, R Matalon, S Weisberg, et al.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.Annals of Clinical and Laboratory Science|May 1, 1982
Keratan and herparan sulfaturia: glucosamine-6-sulfate deficiencyR Matalon, R Wappner, M Deanching, 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.Archives of Pathology & Laboratory Medicine|September 1, 1983
Hunter' syndrome. Ultrastructural features in young childrenJ V Murphy, A E Hodach, E F Gilbert, 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 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.Pageof 13