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R Matalon

Showing results (61-70 of 185) with videos related to

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The Journal of Pediatrics|May 1, 1991
Children of fathers with phenylketonuria: an international surveyR O Fisch, R Matalon, S Weisberg, et al.
Biochemical and Biophysical Research Communications|October 1, 1973
Hunter's syndrome: a deficiency of L-idurono-sulfate sulfataseI Sjöberg, L A Fransson, R Matalon, et al.
Annales De Genetique|September 22, 2000
Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndromeG V Velagaleti, A Kumar, L H Lockhart, et al.
JAMA|December 7, 1970
Intermittent hemodialysis with repeated femoral vein punctureR Matalon, B D Nidus, D Cantacuzino, et al.
Annals of Clinical and Laboratory Science|September 1, 1982
Screening for biopterin defects in newborns with phenylketonuria and other hyperphenylalaninemiasR Matalon, K Michals, C L Lee, et al.
American Journal of Medical Genetics|May 1, 1988
Simpson-Golabi-Behmel syndrome: follow-up of the Michigan familyJ M Opitz, J Herrmann, E F Gilbert, et al.
The Journal of Pediatrics|June 1, 1985
Return to diet therapy in patients with phenylketonuriaK Michals, M Dominik, V Schuett, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 1, 1971
The significance of mucopolysaccharides in amyloidM Pras, Z Nevo, M Schubert, et al.
Clinical Genetics|February 1, 1986
Sanfilippo disease in GreeceN G Beratis, S L Sklower, L Wilbur, 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.
Pageof 19

Showing results (61-70 of 185) with videos related to

Sort By:
Pageof 19
The Journal of Pediatrics|May 1, 1991
Children of fathers with phenylketonuria: an international surveyR O Fisch, R Matalon, S Weisberg, et al.
Biochemical and Biophysical Research Communications|October 1, 1973
Hunter's syndrome: a deficiency of L-idurono-sulfate sulfataseI Sjöberg, L A Fransson, R Matalon, et al.
Annales De Genetique|September 22, 2000
Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndromeG V Velagaleti, A Kumar, L H Lockhart, et al.
JAMA|December 7, 1970
Intermittent hemodialysis with repeated femoral vein punctureR Matalon, B D Nidus, D Cantacuzino, et al.
Annals of Clinical and Laboratory Science|September 1, 1982
Screening for biopterin defects in newborns with phenylketonuria and other hyperphenylalaninemiasR Matalon, K Michals, C L Lee, et al.
American Journal of Medical Genetics|May 1, 1988
Simpson-Golabi-Behmel syndrome: follow-up of the Michigan familyJ M Opitz, J Herrmann, E F Gilbert, et al.
The Journal of Pediatrics|June 1, 1985
Return to diet therapy in patients with phenylketonuriaK Michals, M Dominik, V Schuett, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 1, 1971
The significance of mucopolysaccharides in amyloidM Pras, Z Nevo, M Schubert, et al.
Clinical Genetics|February 1, 1986
Sanfilippo disease in GreeceN G Beratis, S L Sklower, L Wilbur, 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.
Pageof 19