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Journal of Inherited Metabolic Disease|March 6, 2007
Double blind placebo control trial of large neutral amino acids in treatment of PKU: effect on blood phenylalanineR Matalon, K Michals-Matalon, G Bhatia, et al.European Journal of Pediatrics|October 24, 2000
The International Collaborative Study of Maternal Phenylketonuria: status report 1998R Koch, E Friedman, C Azen, et al.American Journal of Ophthalmology|September 1, 1975
A new mucolipidosis with psychomotor retardation, corneal clouding, and retinal degenerationF W Newell, R Matalon, S MeyerTransactions of the American Ophthalmological Society|January 1, 1976
A new mucolipidosis with psychomotor retardation, corneal clouding, and retinal degenerationF W Newell, R Matalon, S MeyerMolecular Syndromology|March 12, 2015
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial SynpolydactylyK Meyertholen, J B Ravnan, R MatalonAmerican Journal of Medical Genetics|January 1, 1987
Dominant inheritance of a syndrome similar to Rubinstein-TaybiP Cotsirilos, J C Taylor, R MatalonThe Journal of Clinical Investigation|September 1, 1975
Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiencyG C Tsay, G Dawson, R MatalonJournal of the American Dental Association (1939)|December 1, 1983
Delayed dental age in hepatorenal glycogen storage diseaseH T Loevy, R Matalon, I M RosenthalOphthalmology|February 1, 1986
Galactokinase activity in patients with idiopathic cataractsM J Elman, M T Miller, R MatalonBiomedical & Environmental Mass Spectrometry|October 1, 1988
Analysis of the pentafluorobenzoyl derivative of phenylethylamine utilizing negative ion chemical ionization and gas chromatography/mass spectrometryP Gashkoff, R Matalon, V Papa, et al.Pageof 12