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Journal Abstract Search


128 related items for PubMed ID: 9051837

  • 1. Oguchi disease: phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin gene.
    Nakazawa M, Wada Y, Fuchs S, Gal A, Tamai M.
    Retina; 1997; 17(1):17-22. PubMed ID: 9051837
    [Abstract] [Full Text] [Related]

  • 2. Oguchi disease with sectoral retinitis pigmentosa harboring adenine deletion at position 1147 in the arrestin gene.
    Nakamachi Y, Nakamura M, Fujii S, Yamamoto M, Okubo K.
    Am J Ophthalmol; 1998 Feb; 125(2):249-51. PubMed ID: 9467455
    [Abstract] [Full Text] [Related]

  • 3. Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene.
    Hayashi T, Tsuzuranuki S, Kozaki K, Urashima M, Tsuneoka H.
    Ophthalmic Res; 2011 Oct; 46(4):175-80. PubMed ID: 21447990
    [Abstract] [Full Text] [Related]

  • 4. A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.
    Hayashi T, Gekka T, Takeuchi T, Goto-Omoto S, Kitahara K.
    Ophthalmology; 2007 Jan; 114(1):134-41. PubMed ID: 17070587
    [Abstract] [Full Text] [Related]

  • 5. Arrestin gene mutations in autosomal recessive retinitis pigmentosa.
    Nakazawa M, Wada Y, Tamai M.
    Arch Ophthalmol; 1998 Apr; 116(4):498-501. PubMed ID: 9565049
    [Abstract] [Full Text] [Related]

  • 6. 1147 del A mutation in the arrestin gene in Japanese patients with Oguchi disease.
    Yamada T, Matsumoto M, Kadoi C, Nagaki Y, Hayasaka Y, Hayasaka S.
    Ophthalmic Genet; 1999 Jun; 20(2):117-20. PubMed ID: 10420197
    [Abstract] [Full Text] [Related]

  • 7. Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations: A Long-Term Follow-up Study.
    Nishiguchi KM, Ikeda Y, Fujita K, Kunikata H, Akiho M, Hashimoto K, Hosono K, Kurata K, Koyanagi Y, Akiyama M, Suzuki T, Kawasaki R, Wada Y, Hotta Y, Sonoda KH, Murakami A, Nakazawa M, Nakazawa T, Abe T.
    Ophthalmology; 2019 Nov; 126(11):1557-1566. PubMed ID: 31257036
    [Abstract] [Full Text] [Related]

  • 8. A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
    Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Yasmeen A, Rogan PK, Caruso R, Sieving PA, Riazuddin S, Hejtmancik JF.
    Mol Vis; 2005 Nov 14; 11():977-85. PubMed ID: 16319817
    [Abstract] [Full Text] [Related]

  • 9. Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-up.
    Liu X, Gao L, Wang G, Long Y, Ren J, Fujinami K, Meng X, Li S.
    Doc Ophthalmol; 2020 Dec 14; 141(3):217-226. PubMed ID: 32333190
    [Abstract] [Full Text] [Related]

  • 10. A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese.
    Fuchs S, Nakazawa M, Maw M, Tamai M, Oguchi Y, Gal A.
    Nat Genet; 1995 Jul 14; 10(3):360-2. PubMed ID: 7670478
    [Abstract] [Full Text] [Related]

  • 11. Wide-field true-colour imaging and clinical characterization of a novel GRK1 mutation in Oguchi disease.
    Ballios BG, Weisbrod D, Kohly R, Muni RH, Wright T, Yan P.
    Doc Ophthalmol; 2020 Oct 14; 141(2):181-185. PubMed ID: 32146548
    [Abstract] [Full Text] [Related]

  • 12.
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  • 13. Novel mutations in the arrestin gene and associated clinical features in Japanese patients with Oguchi's disease.
    Nakamura M, Yamamoto S, Okada M, Ito S, Tano Y, Miyake Y.
    Ophthalmology; 2004 Jul 14; 111(7):1410-4. PubMed ID: 15234147
    [Abstract] [Full Text] [Related]

  • 14. The first case of Oguchi disease, type 2 in a Polish patient with confirmed GRK1 gene mutation.
    Skorczyk-Werner A, Kocięcki J, Wawrocka A, Wicher K, Krawczyńiski MR.
    Klin Oczna; 2015 Jul 14; 117(1):27-30. PubMed ID: 26349155
    [Abstract] [Full Text] [Related]

  • 15. [Oguchi disease or stationary congenital night blindness: a case report].
    Boissonnot M, Robert MF, Gilbert-Dussardier B, Dighiero P.
    J Fr Ophtalmol; 2007 Jan 14; 30(1):e2. PubMed ID: 17287664
    [Abstract] [Full Text] [Related]

  • 16. Oguchi disease masked by retinitis pigmentosa.
    Sonoyama H, Shinoda K, Ishigami C, Tada Y, Ideta H, Ideta R, Takahashi M, Miyake Y.
    Doc Ophthalmol; 2011 Oct 14; 123(2):127-33. PubMed ID: 21922265
    [Abstract] [Full Text] [Related]

  • 17. Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.
    Dryja TP.
    Am J Ophthalmol; 2000 Nov 14; 130(5):547-63. PubMed ID: 11078833
    [Abstract] [Full Text] [Related]

  • 18. Genetic analysis and clinical features of three Chinese patients with Oguchi disease.
    Wei X, Li H, Wu S, Zhu T, Sui R.
    Doc Ophthalmol; 2023 Feb 14; 146(1):17-32. PubMed ID: 36417138
    [Abstract] [Full Text] [Related]

  • 19. A compound heterozygous mutation in the S-Antigen Visual Arrestin SAG gene in a Chinese patient with Oguchi type one: a case report.
    Deng Z, Fan F, Tang D, Wu Y, Shu Y, Wu K.
    BMC Ophthalmol; 2022 Mar 04; 22(1):99. PubMed ID: 35246075
    [Abstract] [Full Text] [Related]

  • 20. Gene analysis and evaluation of the single founder effect in Japanese patients with Oguchi disease.
    Saga M, Mashima Y, Kudoh J, Oguchi Y, Shimizu N.
    Jpn J Ophthalmol; 2004 Mar 04; 48(4):350-2. PubMed ID: 15295660
    [Abstract] [Full Text] [Related]


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