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Journal Abstract Search

210 related items for PubMed ID: 11035549

  • 1.
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  • 2. Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene.
    Eksandh LC, Ponjavic V, Ayyagari R, Bingham EL, Hiriyanna KT, Andréasson S, Ehinger B, Sieving PA.
    Arch Ophthalmol; 2000 Aug; 118(8):1098-104. PubMed ID: 10922205
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  • 5. Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease.
    Eksandh L, Andréasson S, Abrahamson M.
    Ophthalmic Genet; 2005 Sep; 26(3):111-7. PubMed ID: 16272055
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  • 7. Unusual manifestations of x-linked retinoschisis: clinical profile and diagnostic evaluation.
    Shukla D, Rajendran A, Gibbs D, Suganthalakshmi B, Zhang K, Sundaresan P.
    Am J Ophthalmol; 2007 Sep; 144(3):419-423. PubMed ID: 17631851
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  • 8. Four Japanese male patients with juvenile retinoschisis: only three have mutations in the RS1 gene.
    Hayashi T, Omoto S, Takeuchi T, Kozaki K, Ueoka Y, Kitahara K.
    Am J Ophthalmol; 2004 Nov; 138(5):788-98. PubMed ID: 15531314
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  • 9. Japanese X-linked juvenile retinoschisis: conflict of phenotype and genotype with novel mutations in the XLRS1 gene.
    Nakamura M, Ito S, Terasaki H, Miyake Y.
    Arch Ophthalmol; 2001 Oct; 119(10):1553-4. PubMed ID: 11594966
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  • 10. [Identification of mutation of the X-linked juvenile retinoschisis gene].
    Yu P, Li J, Li R, Zhang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):88-91. PubMed ID: 11295123
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  • 11. Long-term follow-up of Stargardt's disease and fundus flavimaculatus.
    Armstrong JD, Meyer D, Xu S, Elfervig JL.
    Ophthalmology; 1998 Mar; 105(3):448-57; discussion 457-8. PubMed ID: 9499775
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  • 12. Retinal pigment epithelial dysfunction in human immunodeficiency virus-infected patients with cytomegalovirus retinitis.
    Harrison JM, van Heuven WA.
    Ophthalmology; 1999 Apr; 106(4):790-7. PubMed ID: 10201604
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  • 13. Identification of four novel mutations of the XLRS1 gene in Japanese patients with X-linked juvenile retinoschisis. Mutation in brief no. 234. Online.
    Mashima Y, Shinoda K, Ishida S, Ozawa Y, Kudoh J, Iwata T, Oguchi Y, Shimizu N.
    Hum Mutat; 1999 Apr; 13(4):338. PubMed ID: 10220153
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  • 14. [X-chromosomal congenital retinoschisis. Clinical aspects and electrophysiology].
    Kellner U, Brümmer S, Foerster MH, Wessing A.
    Fortschr Ophthalmol; 1990 Apr; 87(3):264-8. PubMed ID: 2376375
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  • 17. Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
    Wissinger B, Dangel S, Jägle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T.
    Invest Ophthalmol Vis Sci; 2008 Feb; 49(2):751-7. PubMed ID: 18235024
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  • 18. Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis.
    Orès R, Mohand-Said S, Dhaenens CM, Antonio A, Zeitz C, Augstburger E, Andrieu C, Sahel JA, Audo I.
    Ophthalmology; 2018 Oct; 125(10):1587-1596. PubMed ID: 29739629
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  • 19. Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.
    Booij JC, Boon CJ, van Schooneveld MJ, ten Brink JB, Bakker A, de Jong PT, Hoyng CB, Bergen AA, Klaver CC.
    Ophthalmology; 2010 Jul; 117(7):1415-22. PubMed ID: 20381869
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  • 20. 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; 111(7):1410-4. PubMed ID: 15234147
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