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American Journal of Medical Genetics
|
July 1, 1983
Ruvalcaba-Myhre-Smith syndrome: a case with probable autosomal-dominant inheritance and additional manifestations
J H DiLiberti, R G Weleber, S Budden
Lancet (London, England)
|
December 2, 1978
Vitamin B6 in management of gyrate atrophy of choroid and retina
R G Weleber, N G Kennaway, N R Buist
The New England Journal of Medicine
|
November 24, 1977
Gyrate atrophy of choroid and retina: deficient activity of ornithine ketoacid aminotransferase in cultured skin fibroblasts
N G Kennaway, R G Weleber, N R Buist
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 1, 1987
Retinal dystrophy in Jeune's syndrome
D J Wilson, R G Weleber, R K Beals
International Ophthalmology
|
August 1, 1981
Gyrate atrophy of the choroid and retina. Approaches to therapy
R G Weleber, N G Kennaway, N R Buist
American Journal of Ophthalmology
|
July 15, 1988
Normal alpha-L-fucosidase and other lysosomal enzyme activities in progressive cone dystrophy
V D Stoumbos, R G Weleber, N G Kennaway
Birth Defects Original Article Series
|
January 1, 1982
Gyrate atrophy of the choroid and retina: clinical and biochemical heterogeneity and response to vitamin B6
R G Weleber, M K Wirtz, N G Kennaway
American Journal of Human Genetics
|
July 1, 1980
Gyrate atrophy of the choroid and retina with hyperornithinemia: biochemical and histologic studies and response to vitamin B6
N G Kennaway, R G Weleber, N R Buist
Journal of Inherited Metabolic Disease
|
January 1, 1985
Heterogeneity and complementation analysis of fibroblasts from vitamin B6 responsive and non-responsive patients with gyrate atrophy of the choroid and retina
M K Wirtz, N G Kennaway, R G Weleber
American Journal of Ophthalmology
|
January 15, 1991
Ocular clinicopathologic study of gyrate atrophy
D J Wilson, R G Weleber, W R Green
Page
of 11
Search research articles
Search
Showing results (21-30 of 110) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics
|
July 1, 1983
Ruvalcaba-Myhre-Smith syndrome: a case with probable autosomal-dominant inheritance and additional manifestations
J H DiLiberti, R G Weleber, S Budden
Lancet (London, England)
|
December 2, 1978
Vitamin B6 in management of gyrate atrophy of choroid and retina
R G Weleber, N G Kennaway, N R Buist
The New England Journal of Medicine
|
November 24, 1977
Gyrate atrophy of choroid and retina: deficient activity of ornithine ketoacid aminotransferase in cultured skin fibroblasts
N G Kennaway, R G Weleber, N R Buist
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 1, 1987
Retinal dystrophy in Jeune's syndrome
D J Wilson, R G Weleber, R K Beals
International Ophthalmology
|
August 1, 1981
Gyrate atrophy of the choroid and retina. Approaches to therapy
R G Weleber, N G Kennaway, N R Buist
American Journal of Ophthalmology
|
July 15, 1988
Normal alpha-L-fucosidase and other lysosomal enzyme activities in progressive cone dystrophy
V D Stoumbos, R G Weleber, N G Kennaway
Birth Defects Original Article Series
|
January 1, 1982
Gyrate atrophy of the choroid and retina: clinical and biochemical heterogeneity and response to vitamin B6
R G Weleber, M K Wirtz, N G Kennaway
American Journal of Human Genetics
|
July 1, 1980
Gyrate atrophy of the choroid and retina with hyperornithinemia: biochemical and histologic studies and response to vitamin B6
N G Kennaway, R G Weleber, N R Buist
Journal of Inherited Metabolic Disease
|
January 1, 1985
Heterogeneity and complementation analysis of fibroblasts from vitamin B6 responsive and non-responsive patients with gyrate atrophy of the choroid and retina
M K Wirtz, N G Kennaway, R G Weleber
American Journal of Ophthalmology
|
January 15, 1991
Ocular clinicopathologic study of gyrate atrophy
D J Wilson, R G Weleber, W R Green
Page
of 11