201 related articles for article (PubMed ID: 22674428)
1. Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation.
Renner AB; Walter A; Fiebig BS; Jägle H
Doc Ophthalmol; 2012 Aug; 125(1):81-9. PubMed ID: 22674428
[TBL] [Abstract][Full Text] [Related]
2. OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina.
Katagiri S; Gekka T; Hayashi T; Ida H; Ohashi T; Eto Y; Tsuneoka H
Doc Ophthalmol; 2014 Apr; 128(2):137-48. PubMed ID: 24429551
[TBL] [Abstract][Full Text] [Related]
3. Retinal structure, function, and molecular pathologic features in gyrate atrophy.
Sergouniotis PI; Davidson AE; Lenassi E; Devery SR; Moore AT; Webster AR
Ophthalmology; 2012 Mar; 119(3):596-605. PubMed ID: 22182799
[TBL] [Abstract][Full Text] [Related]
4. Gyrate atrophy of the choroid and retina diagnosed by ornithine-δ-aminotransferase gene analysis: a case report.
Kim SJ; Lim DH; Kim JH; Kang SW
Korean J Ophthalmol; 2013 Oct; 27(5):388-91. PubMed ID: 24082780
[TBL] [Abstract][Full Text] [Related]
5. Variable phenotypes of gyrate atrophy in siblings with a nonsense mutation in
Sen S; Kannan SK; Shanmugam U; Rajan R; Babu N; Vanniarajan A
Ophthalmic Genet; 2021 Jun; 42(3):300-303. PubMed ID: 33463379
[No Abstract] [Full Text] [Related]
6. Reversal of cystoid macular edema in gyrate atrophy patients.
Heller D; Weiner C; Nasie I; Anikster Y; Landau Y; Koren T; Pokroy R; Abulafia A; Pras E
Ophthalmic Genet; 2017 Dec; 38(6):549-554. PubMed ID: 28388263
[TBL] [Abstract][Full Text] [Related]
7. Gyrate atrophy of the choroid and retina: further experience with long-term reduction of ornithine levels in children.
Kaiser-Kupfer MI; Caruso RC; Valle D
Arch Ophthalmol; 2002 Feb; 120(2):146-53. PubMed ID: 11831916
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Gyrate atrophy-like phenotype with normal plasma ornithine.
Kellner U; Weleber RG; Kennaway NG; Fishman GA; Foerster MH
Retina; 1997; 17(5):403-13. PubMed ID: 9355188
[TBL] [Abstract][Full Text] [Related]
11. Use of an arginine-restricted diet to slow progression of visual loss in patients with gyrate atrophy.
Kaiser-Kupfer MI; Caruso RC; Valle D; Reed GF
Arch Ophthalmol; 2004 Jul; 122(7):982-4. PubMed ID: 15249361
[TBL] [Abstract][Full Text] [Related]
12. A possible ocular biomarker for response to hyperornithinemia in gyrate atrophy: the effect of pyridoxine, lysine, and arginine-restricted diet in a patient with advanced disease.
da Palma MM; Ku C; Igelman AD; Burr A; Shevchenko Sutherland L; Koerner C; Valle D; Pennesi ME; Yang P
Ophthalmic Genet; 2023 Apr; 44(2):191-197. PubMed ID: 35856163
[TBL] [Abstract][Full Text] [Related]
13. Metabolic follow-up of a Croatian patient with gyrate atrophy and a new mutation in the
Zekušić M; Škaričić A; Fumić K; Rogić D; Žigman T; Petković Ramadža D; Vukojević N; Rüfenacht V; Uroić V; Barić I
Biochem Med (Zagreb); 2018 Oct; 28(3):030801. PubMed ID: 30429681
[TBL] [Abstract][Full Text] [Related]
14. Gyrate Atrophy of the Choroid and Retina: A Review.
Elnahry AG; Elnahry GA
Eur J Ophthalmol; 2022 May; 32(3):1314-1323. PubMed ID: 34894815
[TBL] [Abstract][Full Text] [Related]
15. Diagnostic value of a combination of next-generation sequencing, chorioretinal imaging and metabolic analysis: lessons from a consanguineous Chinese family with gyrate atrophy of the choroid and retina stemming from a novel OAT variant.
Huang J; Fu J; Fu S; Yang L; Nie K; Duan C; Cheng J; Li Y; Lv H; Chen R; Liu L; Fu J
Br J Ophthalmol; 2019 Mar; 103(3):428-435. PubMed ID: 30366948
[TBL] [Abstract][Full Text] [Related]
16. Gyrate atrophy of the choroid and retina. Long-term reduction of ornithine slows retinal degeneration.
Kaiser-Kupfer MI; Caruso RC; Valle D
Arch Ophthalmol; 1991 Nov; 109(11):1539-48. PubMed ID: 1755734
[TBL] [Abstract][Full Text] [Related]
17. Multimodal characterization of a novel mutation causing vitamin B6-responsive gyrate atrophy.
Cui X; Jauregui R; Park KS; Tsang SH
Ophthalmic Genet; 2018 Aug; 39(4):512-516. PubMed ID: 29757052
[TBL] [Abstract][Full Text] [Related]
18. A Case of Foveoschisis Associated with Ornithine Aminotransferase Deficiency and Gyrate Atrophy.
Ozcaliskan S; Balci S; Artunay O
J Coll Physicians Surg Pak; 2021 Nov; 31(11):1354-1356. PubMed ID: 34689497
[TBL] [Abstract][Full Text] [Related]
19. [Gyrate atrophy and craniopharyngioma: a case report].
Angioï-Duprez K; Maalouf T; George JL
J Fr Ophtalmol; 2001 May; 24(5):513-6. PubMed ID: 11397989
[TBL] [Abstract][Full Text] [Related]
20. Unique case of gyrate atrophy with a well-preserved electroretinogram (ERG).
Jasani KM; Parry NRA; Black G; Kelly SP
BMJ Case Rep; 2018 Feb; 2018():. PubMed ID: 29437727
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
