- ►nih.gov T Wang, G Steel, AH Milam, D Valle - Proceedings of the National Academy of Sciences of …, 2000 - National Acad Sciences Deficiency of ornithine-δ-aminotransferase (OAT) in humans results in gyrate
atrophy of the choroid and retina (GA), an autosomal recessive disorder
characterized by ornithine accumulation and a progressive chorioretinal ... Cited by 24 - Related articles - BL Direct - All 9 versions
- ►nutrition.org PJ Garlick - Journal of Nutrition, 2004 - Am Soc Nutrition In recent years there has been a large increase in the consumption of individual
amino acids as dietary supplements. This has resulted not only from the use of
certain amino acids as flavoring agents, but other amino acids are taken ... Cited by 16 - Related articles - BL Direct - All 9 versions
RG Weleber, NG Kennaway, NRM Buist - International Ophthalmology, 1981 - Springer Gyrate atrophy of the choroid and retina is caused by deficient activity of
ornithine ketoacid amino- transferase, a pyridoxal phosphate dependent enzyme.
Besides the typical eye findings, abnormalities have been found on muscle ... Cited by 14 - Related articles - All 3 versions
Y Mashima, RG Weleber, NG Kennaway, G … - Ophthalmic Genetics, 1999 - informahealthcare.com Correspondence and reprint requests to: George Inana, MD, Ph.D. Laboratory of
Molecular Genetics Bascom Palmer Eye Institute University of Miami School of
Medicine 1638 NW 10th Avenue Miami, FL USA Tel: (305) 326-6509 Fax: (305) ... Cited by 4 - Related articles - BL Direct - All 6 versions
U KELLNER, RG WELEBER, NG KENNAWAY … - Retina, 1997 - journals.lww.com GYRATE ATROPHY-LIKE PHENOTYPE WTTH NORMAL PLASMA ORNITHINE ULRICH KELLNER, MD,*
RICHARD G. WELEBER, MD,ft NANCY G. KENNAWAY, D. Рн1Ь,ф GERALD A. FISHMAN,
MD,§ MICHAEL H. FOERSTER, MD* Purpose: To describe the clinical ... Cited by 2 - Related articles - BL Direct - All 2 versions
- ►nih.gov [PDF] S Hayasaka, T Shiono, K Mizuno, C Sasayama … - British Medical Journal, 1986 - bjo.bmj.com Page 1. doi:10.1136/bjo.70.8.612 1986;70;612-614 Br. J. Ophthalmol. Tanaka,
M Hayakawa, Y Miyake and N Ohba S Hayasaka, T Shiono, K ... Cited by 2 - Related articles - All 7 versions
R Christopher - Indian Pediatrics, 2001 - indianpediatrics.net Hyperornithinemia associated with gyrate atrophy of the choroid and retina is a
rare, autosomal recessive disorder resulting from a deficiency of the
mitochondrial matrix enxyme, ornithine d-aminotransferase (OAT). This ... Related articles - Cached - All 2 versions
HF MICHAEL - RETINA, 1997 - retinascience.de GYRATE ATROPHY-LIKE PHENOTYPE WITH NORMAL PLASMA ORNITHINE ULRTCH KELLNER, MD,*
RICHARD G. WELEBER, MD,t± NANCY G. KENNAWAY, D. Рн1Ь,ф GERALD A. FISHMAN,
MICHAEL H. FOERSTER, MD* MD,§ Purpose: To describe the clinical ... Related articles - All 2 versions
VE Shih, MR Baumgartner - Genetics - Springer Ornithine Metabolism Ornithineisanimportantintermediateinseveralmeta- bolic
pathways. The pyridoxal phosphate requiring en- zyme ornithine-
-aminotransferase (OAT) plays a piv- otal role in its metabolism. During ... Related articles
