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The Journal of Biological Chemistry
|
September 25, 1972
Glycosphingolipids in cultured human skin fibroblasts. I. Characterization and metabolism in normal fibroblasts
G Dawson, R Matalon, A Dorfman
The Journal of Pediatrics
|
October 1, 1995
Canavan disease: from spongy degeneration to molecular analysis
R Matalon, K Michals, R Kaul
Biochemical and Biophysical Research Communications
|
December 23, 1974
Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome
R Matalon, B Arbogast, A Dorfman
Journal of Inherited Metabolic Disease
|
January 1, 1993
Canavan disease: biochemical and molecular studies
R Matalon, R Kaul, K Michals
Biochemical Medicine and Metabolic Biology
|
February 1, 1988
Phenylalanine metabolites as indicators of dietary compliance in children with phenylketonuria
K Michals, M Lopus, R Matalon
Endocrinology
|
October 1, 1972
Metabolism of L-thyroxine (T4) and L-triiodothyronine (T3) by human fibroblasts in tissue culture: evidence for cellular binding proteins and conversion of T4 to T3
S Refetoff, R Matalon, M Bigazzi
The Journal of Pediatrics
|
June 1, 1974
Excretion of mannose-rich complex carbohydrates by a patient with alpha-mannosidase deficiency (mannosidosis)
G C Tsay, G Dawson, R Matalon
Pediatric Research
|
August 1, 1973
Correction of the enzymic defect in cultured fibroblasts from patients with Fabry's disease: treatment with purified alpha-galactosidase from ficin
G Dawson, R Matalon, Y T Li
American Journal of Ophthalmology
|
September 1, 1975
A new mucolipidosis with psychomotor retardation, corneal clouding, and retinal degeneration
F W Newell, R Matalon, S Meyer
Transactions of the American Ophthalmological Society
|
January 1, 1976
A new mucolipidosis with psychomotor retardation, corneal clouding, and retinal degeneration
F W Newell, R Matalon, S Meyer
Page
of 19
Search research articles
Search
Showing results (21-30 of 185) with videos related to
Sort By:
Page
of 19
The Journal of Biological Chemistry
|
September 25, 1972
Glycosphingolipids in cultured human skin fibroblasts. I. Characterization and metabolism in normal fibroblasts
G Dawson, R Matalon, A Dorfman
The Journal of Pediatrics
|
October 1, 1995
Canavan disease: from spongy degeneration to molecular analysis
R Matalon, K Michals, R Kaul
Biochemical and Biophysical Research Communications
|
December 23, 1974
Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome
R Matalon, B Arbogast, A Dorfman
Journal of Inherited Metabolic Disease
|
January 1, 1993
Canavan disease: biochemical and molecular studies
R Matalon, R Kaul, K Michals
Biochemical Medicine and Metabolic Biology
|
February 1, 1988
Phenylalanine metabolites as indicators of dietary compliance in children with phenylketonuria
K Michals, M Lopus, R Matalon
Endocrinology
|
October 1, 1972
Metabolism of L-thyroxine (T4) and L-triiodothyronine (T3) by human fibroblasts in tissue culture: evidence for cellular binding proteins and conversion of T4 to T3
S Refetoff, R Matalon, M Bigazzi
The Journal of Pediatrics
|
June 1, 1974
Excretion of mannose-rich complex carbohydrates by a patient with alpha-mannosidase deficiency (mannosidosis)
G C Tsay, G Dawson, R Matalon
Pediatric Research
|
August 1, 1973
Correction of the enzymic defect in cultured fibroblasts from patients with Fabry's disease: treatment with purified alpha-galactosidase from ficin
G Dawson, R Matalon, Y T Li
American Journal of Ophthalmology
|
September 1, 1975
A new mucolipidosis with psychomotor retardation, corneal clouding, and retinal degeneration
F W Newell, R Matalon, S Meyer
Transactions of the American Ophthalmological Society
|
January 1, 1976
A new mucolipidosis with psychomotor retardation, corneal clouding, and retinal degeneration
F W Newell, R Matalon, S Meyer
Page
of 19