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R Matalon

Showing results (81-90 of 185) with videos related to

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Biochemical and Biophysical Research Communications|November 27, 1974
Morquio's syndrome: deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfataseR Matalon, B Arbogast, P Justice, et al.
Kidney International|February 1, 1972
Repositioning of the basilic vein and superficial femoral artery for chronic hemodialysisB D Nidus, D A Tice, R Matalon, et al.
Clinical Pediatrics|June 1, 1992
A treatment program for adolescents with phenylketonuriaL A Gleason, K Michals, R Matalon, et al.
Journal of Neurochemistry|January 1, 1991
Purification, characterization, and localization of aspartoacylase from bovine brainR Kaul, J Casanova, A B Johnson, 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.
American Journal of Medical Genetics|February 1, 1988
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan diseaseR Matalon, K Michals, D Sebesta, et al.
Neuropediatrics|September 12, 2025
Prenatal Diagnosis of ANKLE2-Related Microcephaly Mimicking Zika InfectionGabrielle R Barsh, Carly M Smith, Dena R Matalon, et al.
Indian Journal of Pediatrics|January 1, 1990
Plasma amino acid patterns in very low birth weight infants during parenteral nutritionG Srinivasan, A Amin, R S Pildes, et al.
Birth Defects Original Article Series|January 1, 1976
Allelic mutations in the mucopolysaccharidosesJ Leisti, D L Rimoin, M Kaback, et al.
American Journal of Medical Genetics|November 24, 1999
Novel missense mutation (Y231C) in a turkish patient with canavan diseaseP L Rady, T Vargas, S K Tyring, et al.
Pageof 19

Showing results (81-90 of 185) with videos related to

Sort By:
Pageof 19
Biochemical and Biophysical Research Communications|November 27, 1974
Morquio's syndrome: deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfataseR Matalon, B Arbogast, P Justice, et al.
Kidney International|February 1, 1972
Repositioning of the basilic vein and superficial femoral artery for chronic hemodialysisB D Nidus, D A Tice, R Matalon, et al.
Clinical Pediatrics|June 1, 1992
A treatment program for adolescents with phenylketonuriaL A Gleason, K Michals, R Matalon, et al.
Journal of Neurochemistry|January 1, 1991
Purification, characterization, and localization of aspartoacylase from bovine brainR Kaul, J Casanova, A B Johnson, 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.
American Journal of Medical Genetics|February 1, 1988
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan diseaseR Matalon, K Michals, D Sebesta, et al.
Neuropediatrics|September 12, 2025
Prenatal Diagnosis of ANKLE2-Related Microcephaly Mimicking Zika InfectionGabrielle R Barsh, Carly M Smith, Dena R Matalon, et al.
Indian Journal of Pediatrics|January 1, 1990
Plasma amino acid patterns in very low birth weight infants during parenteral nutritionG Srinivasan, A Amin, R S Pildes, et al.
Birth Defects Original Article Series|January 1, 1976
Allelic mutations in the mucopolysaccharidosesJ Leisti, D L Rimoin, M Kaback, et al.
American Journal of Medical Genetics|November 24, 1999
Novel missense mutation (Y231C) in a turkish patient with canavan diseaseP L Rady, T Vargas, S K Tyring, et al.
Pageof 19