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Journal Abstract Search

391 related items for PubMed ID: 7943119

  • 21. No pigment deposition in a patient with advanced retinitis punctata albescens.
    Fujii M, Hayasaka S.
    Ophthalmologica; 1994; 208(6):339-41. PubMed ID: 7845653
    [Abstract] [Full Text] [Related]

  • 22. Acute retinal pigment epitheliitis.
    Luttrull JK, Chittum ME.
    Am J Ophthalmol; 1995 Sep; 120(3):389-91. PubMed ID: 7661213
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  • 23. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
    Jacobson SG, Buraczynska M, Milam AH, Chen C, Järvaläinen M, Fujita R, Wu W, Huang Y, Cideciyan AV, Swaroop A.
    Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1983-97. PubMed ID: 9331262
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  • 24. Retinal dystrophies caused by mutations in RPE65: assessment of visual functions.
    Hamel CP, Griffoin JM, Lasquellec L, Bazalgette C, Arnaud B.
    Br J Ophthalmol; 2001 Apr; 85(4):424-7. PubMed ID: 11264131
    [Abstract] [Full Text] [Related]

  • 25. MULTIMODAL IMAGING OF CRB1 RETINITIS PIGMENTOSA WITH A PERIPHERAL RETINAL TUMOR.
    Corvi F, Juhn A, Corradetti G, Nguyen TV, Fawzi AA, Sarraf D, Sadda SR.
    Retin Cases Brief Rep; 2022 Jul 01; 16(4):407-410. PubMed ID: 32976229
    [Abstract] [Full Text] [Related]

  • 26. Associated retinitis pigmentosa and fundus flavimaculatus.
    Fiore C, Santoni G, Lupidi G, Ricci AL.
    Ophthalmologica; 1987 Jul 01; 194(2-3):111-8. PubMed ID: 3614843
    [Abstract] [Full Text] [Related]

  • 27. Retinitis Pigmentosa (Non-syndromic).
    Tsang SH, Sharma T.
    Adv Exp Med Biol; 2018 Jul 01; 1085():125-130. PubMed ID: 30578498
    [Abstract] [Full Text] [Related]

  • 28. Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease.
    Kniazeva MF, Chiang MF, Cutting GR, Zack DJ, Han M, Zhang K.
    Ophthalmic Genet; 1999 Jun 01; 20(2):71-81. PubMed ID: 10420191
    [Abstract] [Full Text] [Related]

  • 29. Concurrent retinitis pigmentosa and pigmented paravenous retinochoroidal atrophy phenotypes in the same patient.
    Ratra D, Chandrasekharan DP, Aruldas P, Ratra V.
    Indian J Ophthalmol; 2016 Oct 01; 64(10):775-777. PubMed ID: 27905344
    [Abstract] [Full Text] [Related]

  • 30. A novel mutation confirms MFRP as the gene causing the syndrome of nanophthalmos-renititis pigmentosa-foveoschisis-optic disk drusen.
    Crespí J, Buil JA, Bassaganyas F, Vela-Segarra JI, Díaz-Cascajosa J, Ayala-Ramírez R, Zenteno JC.
    Am J Ophthalmol; 2008 Aug 01; 146(2):323-328. PubMed ID: 18554571
    [Abstract] [Full Text] [Related]

  • 31. Preliminary report: indications of improved visual function after retinal sheet transplantation in retinitis pigmentosa patients.
    Radtke ND, Aramant RB, Seiler M, Petry HM.
    Am J Ophthalmol; 1999 Sep 01; 128(3):384-7. PubMed ID: 10511047
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  • 38. X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.
    Fishman GA, Grover S, Jacobson SG, Alexander KR, Derlacki DJ, Wu W, Buraczynska M, Swaroop A.
    Ophthalmology; 1998 Dec 01; 105(12):2286-96. PubMed ID: 9855162
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  • 39. Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC).
    van Soest S, te Nijenhuis S, van den Born LI, Bleeker-Wagemakers EM, Sharp E, Sandkuijl LA, Westerveld A, Bergen AA.
    Cytogenet Cell Genet; 1996 Dec 01; 73(1-2):81-5. PubMed ID: 8646891
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  • 40. Frequency of optic disc or parapapillary nerve fiber layer drusen in retinitis pigmentosa.
    Grover S, Fishman GA, Brown J.
    Ophthalmology; 1997 Feb 01; 104(2):295-8. PubMed ID: 9052635
    [Abstract] [Full Text] [Related]

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