277 related articles for article (PubMed ID: 7240420)
21. At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.
Mitchell GA; Brody LC; Sipila I; Looney JE; Wong C; Engelhardt JF; Patel AS; Steel G; Obie C; Kaiser-Kupfer M
Proc Natl Acad Sci U S A; 1989 Jan; 86(1):197-201. PubMed ID: 2492100
[TBL] [Abstract][Full Text] [Related]
22. [Gyrate atrophy of choroid and retina, and hyperornithinemia].
Sela BA; Zlotnik J; Masos T; Yablonski G; Abraham F
Harefuah; 2000 Jan; 138(2):101-5, 175. PubMed ID: 10883069
[TBL] [Abstract][Full Text] [Related]
23. Heterogeneity and complementation analysis of fibroblasts from vitamin B6 responsive and non-responsive patients with gyrate atrophy of the choroid and retina.
Wirtz MK; Kennaway NG; Weleber RG
J Inherit Metab Dis; 1985; 8(2):71-4. PubMed ID: 3939534
[TBL] [Abstract][Full Text] [Related]
24. Purification and properties of ornithine aminotransferase from rat brain.
Deshmukh DR; Srivastava SK
Experientia; 1984 Apr; 40(4):357-9. PubMed ID: 6425075
[TBL] [Abstract][Full Text] [Related]
25. Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase.
Peltola KE; Näntö-Salonen K; Heinonen OJ; Jääskeläinen S; Heinänen K; Simell O; Nikoskelainen E
Ophthalmology; 2001 Apr; 108(4):721-9. PubMed ID: 11297489
[TBL] [Abstract][Full Text] [Related]
26. Molecular and cellular basis of ornithine δ-aminotransferase deficiency caused by the V332M mutation associated with gyrate atrophy of the choroid and retina.
Montioli R; Desbats MA; Grottelli S; Doimo M; Bellezza I; Borri Voltattorni C; Salviati L; Cellini B
Biochim Biophys Acta Mol Basis Dis; 2018 Nov; 1864(11):3629-3638. PubMed ID: 30251682
[TBL] [Abstract][Full Text] [Related]
27. Low-protein diet and progression of retinal degeneration in gyrate atrophy of the choroid and retina: a twenty-six-year follow-up.
Santinelli R; Costagliola C; Tolone C; D'Aloia A; D'Avanzo A; Prisco F; Perrone L; del Giudice EM
J Inherit Metab Dis; 2004; 27(2):187-96. PubMed ID: 15159649
[TBL] [Abstract][Full Text] [Related]
28. Gyrate atrophy with hyperornithinaemia: different types of responsiveness to vitamin B6.
Hayasaka S; Saito T; Nakajima H; Takaku Y; Shiono T; Mizuno K; Ohmura K; Tada K
Br J Ophthalmol; 1981 Jul; 65(7):478-83. PubMed ID: 7260021
[TBL] [Abstract][Full Text] [Related]
29. Gyrate atrophy of the retina: inborn error of L-ornithin:2-oxoacid aminotransferase.
O'Donnell JJ; Sandman RP; Martin SR
Science; 1978 Apr; 200(4338):200-1. PubMed ID: 635581
[TBL] [Abstract][Full Text] [Related]
30. Gyrate atrophy of the choroid and retina. Approaches to therapy.
Weleber RG; Kennaway NG; Buist NR
Int Ophthalmol; 1981 Aug; 4(1-2):23-32. PubMed ID: 7028650
[TBL] [Abstract][Full Text] [Related]
31. Gyrate atrophy of the choroid and retina. Early findings.
Kaiser-Kupfer MI; Ludwig IH; de Monasterio FM; Valle D; Krieger I
Ophthalmology; 1985 Mar; 92(3):394-401. PubMed ID: 3991128
[TBL] [Abstract][Full Text] [Related]
32. Ornithine delta-aminotransferase activity in retina and other tissues.
Rao GN; Cotlier E
Neurochem Res; 1984 Apr; 9(4):555-62. PubMed ID: 6462326
[TBL] [Abstract][Full Text] [Related]
33. Treatment of gyrate atrophy of the choroid and retina with low arginine diet.
McInnes RR; Arshinoff SA; Bell L; McCulloch C
Trans Am Ophthalmol Soc; 1980; 78():226-42. PubMed ID: 7257057
[TBL] [Abstract][Full Text] [Related]
34. Liver-directed gene therapy for ornithine aminotransferase deficiency.
Boffa I; Polishchuk E; De Stefano L; Dell'Aquila F; Nusco E; Marrocco E; Audano M; Pedretti S; Caterino M; Bellezza I; Ruoppolo M; Mitro N; Cellini B; Auricchio A; Brunetti-Pierri N
EMBO Mol Med; 2023 Apr; 15(4):e17033. PubMed ID: 36647689
[TBL] [Abstract][Full Text] [Related]
35. Hyperornithinemia and gyrate atrophy of choroid and retina. Report of a case.
Stoppoloni G; Prisco F; Santinelli R; Tolone C
Helv Paediatr Acta; 1978 Nov; 33(4-5):429-33. PubMed ID: 711502
[TBL] [Abstract][Full Text] [Related]
36. Pyridoxine effects on ornithine ketoacid transaminase activity in fibroblasts from carriers of two forms of gyrate atrophy of the choroid and retina.
Shih VE; Mandell R; Berson EL
Am J Hum Genet; 1988 Dec; 43(6):929-33. PubMed ID: 3195590
[TBL] [Abstract][Full Text] [Related]
37. Deficient L-ornithine: 2-oxoacid aminotransferase activity in cultured fibroblasts from a patient with gyrate atrophy of the retina.
O'Donnell JJ; Sandman RP; Martin SR
Biochem Biophys Res Commun; 1977 Nov; 79(2):396-9. PubMed ID: 588272
[No Abstract] [Full Text] [Related]
38. Human ornithine aminotransferase complexed with L-canaline and gabaculine: structural basis for substrate recognition.
Shah SA; Shen BW; Brünger AT
Structure; 1997 Aug; 5(8):1067-75. PubMed ID: 9309222
[TBL] [Abstract][Full Text] [Related]
39. Raised plasma-ornithine and gyrate atrophy of the choroid and retina.
Simell O; Takki K
Lancet; 1973 May; 1(7811):1031-3. PubMed ID: 4122112
[No Abstract] [Full Text] [Related]
40. Biochemical and Bioinformatic Studies of Mutations of Residues at the Monomer-Monomer Interface of Human Ornithine Aminotransferase Leading to Gyrate Atrophy of Choroid and Retina.
Floriani F; Borri Voltattorni C; Cellini B; Montioli R
Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36834788
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]