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R Matalon

Showing results (51-60 of 185) with videos related to

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Nature Genetics|October 1, 1993
Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan diseaseR Kaul, G P Gao, K Balamurugan, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1985
Craniofacial and mucopolysaccharide abnormalities in Kniest dysplasiaH Friede, R Matalon, V Harris, et al.
Lancet (London, England)|June 25, 1977
Glucose-6-phosphatase activity in human placenta: Possible detection of heterozygote for glycogen-storage disease type IR Matalon, K Michals, P Justice, et al.
Gene Therapy|August 1, 1995
Overexpression of arylsulfatase A gene in fibroblasts from metachromatic leukodystrophy patients does not induce a new phenotypeT Ohashi, R Matalon, J A Barranger, et al.
Genomics|May 15, 1994
Canavan disease: genomic organization and localization of human ASPA to 17p13-ter and conservation of the ASPA gene during evolutionR Kaul, K Balamurugan, G P Gao, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Canavan disease: molecular basis of aspartoacylase deficiencyR Kaul, G P Gao, K Balamurugan, et al.
American Journal of Diseases of Children (1960)|January 1, 1981
Foamy histiocytes in the CSF of a patient with infantile Niemann-Pick diseaseR R Chilcote, M Miller, G Dawson, et al.
Pediatrics|April 1, 1983
Nonketotic hyperglycinemia: treatment with diazepam--a competitor for glycine receptorsR Matalon, S Naidu, J R Hughes, et al.
Biochemical Medicine|August 1, 1983
Glucose-6-phosphatase as a marker for tumors of liver and kidney originK Michals, K Pringle, E J Pang, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
The use of deuterated phenylalanine for the in vivo assay of phenylalanine hydroxylase activity in childrenR Matalon, D E Matthews, K Michals, et al.
Pageof 19

Showing results (51-60 of 185) with videos related to

Sort By:
Pageof 19
Nature Genetics|October 1, 1993
Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan diseaseR Kaul, G P Gao, K Balamurugan, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1985
Craniofacial and mucopolysaccharide abnormalities in Kniest dysplasiaH Friede, R Matalon, V Harris, et al.
Lancet (London, England)|June 25, 1977
Glucose-6-phosphatase activity in human placenta: Possible detection of heterozygote for glycogen-storage disease type IR Matalon, K Michals, P Justice, et al.
Gene Therapy|August 1, 1995
Overexpression of arylsulfatase A gene in fibroblasts from metachromatic leukodystrophy patients does not induce a new phenotypeT Ohashi, R Matalon, J A Barranger, et al.
Genomics|May 15, 1994
Canavan disease: genomic organization and localization of human ASPA to 17p13-ter and conservation of the ASPA gene during evolutionR Kaul, K Balamurugan, G P Gao, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Canavan disease: molecular basis of aspartoacylase deficiencyR Kaul, G P Gao, K Balamurugan, et al.
American Journal of Diseases of Children (1960)|January 1, 1981
Foamy histiocytes in the CSF of a patient with infantile Niemann-Pick diseaseR R Chilcote, M Miller, G Dawson, et al.
Pediatrics|April 1, 1983
Nonketotic hyperglycinemia: treatment with diazepam--a competitor for glycine receptorsR Matalon, S Naidu, J R Hughes, et al.
Biochemical Medicine|August 1, 1983
Glucose-6-phosphatase as a marker for tumors of liver and kidney originK Michals, K Pringle, E J Pang, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
The use of deuterated phenylalanine for the in vivo assay of phenylalanine hydroxylase activity in childrenR Matalon, D E Matthews, K Michals, et al.
Pageof 19