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343 related items for PubMed ID: 17631851

  • 1. 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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  • 2. 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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  • 3. 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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  • 5. A phenotype-genotype correlation study of X-linked retinoschisis.
    Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE.
    Ophthalmology; 2013 Jul; 120(7):1454-64. PubMed ID: 23453514
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  • 6. Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
    Hayashi T, Gekka T, Goto-Omoto S, Takeuchi T, Kubo A, Kitahara K.
    Ophthalmology; 2005 Dec; 112(12):2115. PubMed ID: 16225923
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  • 7. Optical coherence tomography in the diagnosis of juvenile X-linked retinoschisis.
    Eriksson U, Larsson E, Holmström G.
    Acta Ophthalmol Scand; 2004 Apr; 82(2):218-23. PubMed ID: 15043546
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  • 8. Natural course of macular retinoschisis in highly myopic eyes without macular hole or retinal detachment.
    Shimada N, Ohno-Matsui K, Baba T, Futagami S, Tokoro T, Mochizuki M.
    Am J Ophthalmol; 2006 Sep; 142(3):497-500. PubMed ID: 16935601
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  • 9. A novel gene mutation in a family with X-linked retinoschisis.
    Lai YH, Huang SP, Chen SP, Hu PS, Lin SF, Sheu MM, Wang HZ, Tsai RK.
    J Formos Med Assoc; 2015 Sep; 114(9):872-80. PubMed ID: 24529551
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  • 10. Clinical characteristics of 14 japanese patients with X-linked juvenile retinoschisis associated with XLRS1 mutation.
    Shinoda K, Ishida S, Oguchi Y, Mashima Y.
    Ophthalmic Genet; 2000 Sep; 21(3):171-80. PubMed ID: 11035549
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  • 11. DNA analysis for diagnosis of x-linked juvenile retinoschisis when clinical examination is difficult in a young child.
    Kawano T, Sato M, Hikoya A, Nishimura K, Hotta Y.
    Jpn J Ophthalmol; 2005 Sep; 49(3):268-70. PubMed ID: 15944839
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  • 15. 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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  • 16. High-definition optical coherence tomography features in vitelliform macular dystrophy.
    Querques G, Regenbogen M, Quijano C, Delphin N, Soubrane G, Souied EH.
    Am J Ophthalmol; 2008 Oct; 146(4):501-507. PubMed ID: 18619572
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  • 19. Macular spectral-domain optical coherence tomography in patients with X linked retinoschisis.
    Gregori NZ, Berrocal AM, Gregori G, Murray TG, Knighton RW, Flynn HW, Dubovy S, Puliafito CA, Rosenfeld PJ.
    Br J Ophthalmol; 2009 Mar; 93(3):373-8. PubMed ID: 19019942
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