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Clinical Pediatrics|June 1, 1992
A treatment program for adolescents with phenylketonuriaL A Gleason, K Michals, R Matalon, et al.The American Journal of Clinical Nutrition|August 1, 1985
Phenylalanine metabolites, attention span and hyperactivityK Michals, R MatalonClinical Biochemistry|August 1, 1991
Phenylketonuria: screening, treatment and maternal PKUR Matalon, K MichalsAdvances in Pediatrics|January 25, 2000
Recent advances in Canavan diseaseR Matalon, K Michals-MatalonNeurochemical Research|May 5, 1999
Biochemistry and molecular biology of Canavan diseaseR Matalon, K Michals-MatalonAnnals of the New York Academy of Sciences|January 1, 1986
Maternal PKU: strategies for dietary treatment and monitoring complianceR Matalon, K Michals, L GleasonThe Journal of Pediatrics|October 1, 1995
Canavan disease: from spongy degeneration to molecular analysisR Matalon, K Michals, R KaulJournal of Inherited Metabolic Disease|January 1, 1993
Canavan disease: biochemical and molecular studiesR Matalon, R Kaul, K MichalsBiochemical Medicine and Metabolic Biology|February 1, 1988
Phenylalanine metabolites as indicators of dietary compliance in children with phenylketonuriaK Michals, M Lopus, R MatalonJournal of Inherited Metabolic Disease|January 1, 1988
Carrier detection for Sanfilippo A syndromeR Matalon, M Deanching, R Marback, et al.Pageof 96