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R Matalon

Showing results (171-180 of 185) with videos related to

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The New England Journal of Medicine|June 10, 1982
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretionM L Batshaw, S Brusilow, L Waber, et al.
Molecular Genetics and Metabolism|June 22, 2021
Progression of vertebral bone disease in mucopolysaccharidosis VII dogs from birth to skeletal maturitySun H Peck, Yian Khai Lau, Jennifer L Kang, et al.
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.
Annals of Neurology|July 14, 2000
Aspartoacylase gene transfer to the mammalian central nervous system with therapeutic implications for Canavan diseaseP Leone, C G Janson, L Bilaniuk, et al.
Acta Neuropathologica|November 15, 2000
Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndromeK Wong, R C Armstrong, K A Gyure, 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.
The Journal of Gene Medicine|July 14, 2000
Knock-out mouse for Canavan disease: a model for gene transfer to the central nervous systemR Matalon, P L Rady, K A Platt, et al.
JAMA|February 22, 2000
Outcome at age 4 years in offspring of women with maternal phenylketonuria: the Maternal PKU Collaborative StudyS E Waisbren, W Hanley, H L Levy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 6, 2018
ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosisCole A Deisseroth, Johannes Birgmeier, Ethan E Bodle, et al.
Prenatal Diagnosis|August 26, 2023
Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletionsCourtney P Verscaj, Frances Velez-Bartolomei, Ethan Bodle, et al.
Pageof 19

Showing results (171-180 of 185) with videos related to

Sort By:
Pageof 19
The New England Journal of Medicine|June 10, 1982
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretionM L Batshaw, S Brusilow, L Waber, et al.
Molecular Genetics and Metabolism|June 22, 2021
Progression of vertebral bone disease in mucopolysaccharidosis VII dogs from birth to skeletal maturitySun H Peck, Yian Khai Lau, Jennifer L Kang, et al.
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.
Annals of Neurology|July 14, 2000
Aspartoacylase gene transfer to the mammalian central nervous system with therapeutic implications for Canavan diseaseP Leone, C G Janson, L Bilaniuk, et al.
Acta Neuropathologica|November 15, 2000
Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndromeK Wong, R C Armstrong, K A Gyure, 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.
The Journal of Gene Medicine|July 14, 2000
Knock-out mouse for Canavan disease: a model for gene transfer to the central nervous systemR Matalon, P L Rady, K A Platt, et al.
JAMA|February 22, 2000
Outcome at age 4 years in offspring of women with maternal phenylketonuria: the Maternal PKU Collaborative StudyS E Waisbren, W Hanley, H L Levy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 6, 2018
ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosisCole A Deisseroth, Johannes Birgmeier, Ethan E Bodle, et al.
Prenatal Diagnosis|August 26, 2023
Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletionsCourtney P Verscaj, Frances Velez-Bartolomei, Ethan Bodle, et al.
Pageof 19