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Proceedings of the National Academy of Sciences of the United States of America|February 1, 1976
The mucopolysaccharidoses (a review)A Dorfman, R MatalonAmerican Journal of Public Health|January 1, 1985
Reinstitution of diet therapy in PKU patients from twenty-two US clinicsV E Schuett, E S Brown, K MichalsThe Journal of Clinical Investigation|October 1, 1974
Sanfilippo A syndrome: sulfamidase deficiency in cultured skin fibroblasts and liverR Matalon, A DorfmanJournal 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.Medicina Cutanea Ibero-Latino-Americana|January 1, 1983
[Neuro-oculo-cutaneous syndrome with multiple sebaceous nevi. Presentation of a case]A L Bittencourt, R Marback, M J Peralta, 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 MatalonPageof 13