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23. Retinitis pigmentosa genetics: a study in Indian population. Vinchurkar MS; Sathye SM; Dikshit M Indian J Ophthalmol; 1996 Jun; 44(2):77-82. PubMed ID: 8916593 [TBL] [Abstract][Full Text] [Related]
24. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation. Zhang Q; Zulfiqar F; Riazuddin SA; Xiao X; Ahmad Z; Riazuddin S; Hejtmancik JF Mol Vis; 2004 Nov; 10():884-9. PubMed ID: 15570217 [TBL] [Abstract][Full Text] [Related]
25. Novel RDH5 mutation in family with mother having fundus albipunctatus and three children with retinitis pigmentosa. Wang C; Nakanishi N; Ohishi K; Hikoya A; Koide K; Sato M; Nakamura M; Hotta Y; Minoshima S Ophthalmic Genet; 2008 Mar; 29(1):29-32. PubMed ID: 18363170 [TBL] [Abstract][Full Text] [Related]
26. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families. Riazuddin SA; Zulfiqar F; Zhang Q; Sergeev YV; Qazi ZA; Husnain T; Caruso R; Riazuddin S; Sieving PA; Hejtmancik JF Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2264-70. PubMed ID: 15980210 [TBL] [Abstract][Full Text] [Related]
27. [A Chinese family with autosomal dominant retinitis pigmentosa and a pro347Leu rhodopsin gene mutation]. Yang H; Luo C; Zhou J; Yan M Chin Med J (Engl); 2000 Jun; 113(6):574-6. PubMed ID: 11775885 [No Abstract] [Full Text] [Related]
28. [Screening of candidate genes in a family with autosomal dominant retinitis pigmentosa]. Teng Y; Tian H; Wang H; Hu X; Chen Y; Yang Z; Wang W Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):164-6. PubMed ID: 12673590 [TBL] [Abstract][Full Text] [Related]
29. [Genetic study of retinal pigmentary dystrophy (retinitis pigmentosa) in Japan]. Tanabe U Jinrui Idengaku Zasshi; 1972 Mar; 16(3):119-53. PubMed ID: 5065755 [No Abstract] [Full Text] [Related]
30. Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa. Martinez-Gimeno M; Maseras M; Baiget M; Beneito M; Antiñolo G; Ayuso C; Carballo M Hum Mutat; 2001 Jun; 17(6):520. PubMed ID: 11385710 [TBL] [Abstract][Full Text] [Related]
31. Homozygous and heterozygous gly-188-Arg mutation of the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa. Reig CM; Trujillo JM; Martinez-Gimeno MM; Garcia-Sandoval BM; Calvo TM; Ayuso C; Carballo M Ophthalmic Genet; 2000 Jun; 21(2):79-87. PubMed ID: 10916182 [TBL] [Abstract][Full Text] [Related]
32. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa. Ayuso C; Garcia-Sandoval B; Najera C; Valverde D; Carballo M; Antiñolo G Clin Genet; 1995 Sep; 48(3):120-2. PubMed ID: 8556816 [TBL] [Abstract][Full Text] [Related]
33. A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu. Ponjavic V; Abrahamson M; Andréasson S; Ehinger B; Fex G; Polland W Ophthalmic Genet; 1997 Jun; 18(2):63-70. PubMed ID: 9228242 [TBL] [Abstract][Full Text] [Related]
35. Novel 2336-2337delCT mutation in RP1 gene in a Japanese family with autosomal dominant retinitis pigmentosa. Kawamura M; Wada Y; Noda Y; Itabashi T; Ogawa S; Sato H; Tanaka K; Ishibashi T; Tamai M Am J Ophthalmol; 2004 Jun; 137(6):1137-9. PubMed ID: 15183808 [TBL] [Abstract][Full Text] [Related]
36. A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa. Grover S; Fishman GA; Stone EM Ophthalmology; 2004 Oct; 111(10):1910-6. PubMed ID: 15465556 [TBL] [Abstract][Full Text] [Related]
38. [Possible role of altered levels of plasma docosahexaenoic acid in the pathogenesis of retinitis pigmentosa. Preliminary results]. Simonelli F; Milone A; Iura A; Picardi C; La Banca AM; Cotticelli L; Rinaldi E Boll Soc Ital Biol Sper; 1990 Sep; 66(9):893-8. PubMed ID: 2149985 [TBL] [Abstract][Full Text] [Related]
39. [Correlation of different ocular diseases of dominant inheritance. Examination of a family with microcornea, high myopia, retinitis pigmentosa, cataract and glaucoma (author's transl)]. Schlieter F; Schroeder U Klin Monbl Augenheilkd; 1974 Apr; 164(4):485-9. PubMed ID: 4843833 [No Abstract] [Full Text] [Related]
40. [Hereditary ataxia, retinal pigment degeneration, hypobetalipoproteinemia]. Lenz H; Pürgyi P Wien Med Wochenschr; 1969 Jun; 119(25):499-500. PubMed ID: 5802411 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]