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R Matalon

Showing results (71-80 of 185) with videos related to

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Lancet (London, England)|January 10, 1970
A chemical method for the antenatal diagnosis of mucopolysaccharidosesR Matalon, A Dorfman, H L Nadler, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Isovaleric acidaemia in a premature infant: diagnosis and treatmentR Heimler, H Hennes, S Khayata, et al.
American Journal of Ophthalmology|November 1, 1973
Retinopathy in childhood dermatomyositisS M Harrison, M Frenkel, B J Grossman, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Folic acid responsive rages, seizures and homocystinuriaJ V Murphy, L M Thome, K Michals, et al.
Prenatal Diagnosis|January 1, 2024
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20CCourtney P Verscaj, Carly Smith, Margaret Homeyer, et al.
Biochemical and Biophysical Research Communications|January 20, 1975
Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndromeE Shapira, R R DeGregorio, R Matalon, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1994
Lipoprotein glomerulopathy: first report in a Chinese maleP Zhang, R Matalon, L Kaplan, et al.
Science (New York, N.Y.)|August 31, 1973
N-acetyl-beta-hexosaminidase: role in the degradation of glycosaminoglycansJ N Thompson, A C Stoolmiller, R Matalon, et al.
Nephron|January 1, 1971
An improved needle set for fistula hemodialysisB D Nidus, R Matalon, P Deutsch, et al.
American Journal of Diseases of Children (1960)|July 1, 1987
Phenotypic features of patients with congenital adrenal hypoplasia and glycerol kinase deficiencyJ E Wise, R Matalon, A M Morgan, et al.
Pageof 19

Showing results (71-80 of 185) with videos related to

Sort By:
Pageof 19
Lancet (London, England)|January 10, 1970
A chemical method for the antenatal diagnosis of mucopolysaccharidosesR Matalon, A Dorfman, H L Nadler, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Isovaleric acidaemia in a premature infant: diagnosis and treatmentR Heimler, H Hennes, S Khayata, et al.
American Journal of Ophthalmology|November 1, 1973
Retinopathy in childhood dermatomyositisS M Harrison, M Frenkel, B J Grossman, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Folic acid responsive rages, seizures and homocystinuriaJ V Murphy, L M Thome, K Michals, et al.
Prenatal Diagnosis|January 1, 2024
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20CCourtney P Verscaj, Carly Smith, Margaret Homeyer, et al.
Biochemical and Biophysical Research Communications|January 20, 1975
Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndromeE Shapira, R R DeGregorio, R Matalon, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1994
Lipoprotein glomerulopathy: first report in a Chinese maleP Zhang, R Matalon, L Kaplan, et al.
Science (New York, N.Y.)|August 31, 1973
N-acetyl-beta-hexosaminidase: role in the degradation of glycosaminoglycansJ N Thompson, A C Stoolmiller, R Matalon, et al.
Nephron|January 1, 1971
An improved needle set for fistula hemodialysisB D Nidus, R Matalon, P Deutsch, et al.
American Journal of Diseases of Children (1960)|July 1, 1987
Phenotypic features of patients with congenital adrenal hypoplasia and glycerol kinase deficiencyJ E Wise, R Matalon, A M Morgan, et al.
Pageof 19