Ocular and Biochemical Abnormalities in Gyrate Atrophy of the Choroid and Retina
- 1 October 1978
- journal article
- Published by Elsevier in Ophthalmology
- Vol. 85 (10) , 1018-1027
- https://doi.org/10.1016/s0161-6420(78)35588-3
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Mucopolysaccharidosis III A (Sanfilippo A disease): Deficiency of a heparin sulfamidase in skin fibroblasts and leucocytesPublished by Elsevier ,2004
- Atypical Retinitis Pigmentosa in Familial HypobetalipoproteinemiaAmerican Journal of Ophthalmology, 1976
- Plasma amino-acids in hereditary retinal disease. Ornithine, lysine, and taurine.British Journal of Ophthalmology, 1976
- Gyrate atrophy of the choroid and retina associated with hyperornithinaemia.British Journal of Ophthalmology, 1974
- Sanfilippo B disease: Serum assays for detection of homozygous and heterozygous individuals in three familiesThe Journal of Pediatrics, 1973
- The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate SulfataseProceedings of the National Academy of Sciences, 1973
- RAISED PLASMA-ORNITHINE AND GYRATE ATROPHY OF THE CHOROID AND RETINAThe Lancet, 1973
- The Defect in the Hurler and Scheie Syndromes: Deficiency of α-L-IduronidaseProceedings of the National Academy of Sciences, 1972
- Phytanic Acid in Patients With Refsum's Syndrome and Response to Dietary TreatmentArchives of internal medicine (1960), 1970
- Electroretinography and Fundus Oculi Findings in Hurler's Disease and Allied MucopolysaccharidosesArchives of Ophthalmology (1950), 1965