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Results: 1 to 20 of 57

1.

Novel compound heterozygous TULP1 mutations in a family with severe early-onset retinitis pigmentosa.

den Hollander AI, van Lith-Verhoeven JJ, Arends ML, Strom TM, Cremers FP, Hoyng CB.

Arch Ophthalmol. 2007 Jul;125(7):932-5.

PMID:
17620573
[PubMed - indexed for MEDLINE]
2.

Gene mutations in retinitis pigmentosa and their clinical implications.

Wang DY, Chan WM, Tam PO, Baum L, Lam DS, Chong KK, Fan BJ, Pang CP.

Clin Chim Acta. 2005 Jan;351(1-2):5-16. Review.

PMID:
15563868
[PubMed - indexed for MEDLINE]
3.

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

al-Maghtheh M, Gregory C, Inglehearn C, Hardcastle A, Bhattacharya S.

Hum Mutat. 1993;2(4):249-55. Review.

PMID:
8401533
[PubMed - indexed for MEDLINE]
4.

Update on the molecular genetics of retinitis pigmentosa.

Wang Q, Chen Q, Zhao K, Wang L, Wang L, Traboulsi EI.

Ophthalmic Genet. 2001 Sep;22(3):133-54. Review.

PMID:
11559856
[PubMed - indexed for MEDLINE]
5.

[From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa].

Cremers FP, Maugeri A, Klevering BJ, Hoefsloot LH, Hoyng CB.

Ned Tijdschr Geneeskd. 2002 Aug 24;146(34):1581-4. Review. Dutch.

PMID:
12224481
[PubMed - indexed for MEDLINE]
6.

A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes.

Phelan JK, Bok D.

Mol Vis. 2000 Jul 8;6:116-24. Review.

PMID:
10889272
[PubMed - indexed for MEDLINE]
Free Article
7.

Genetic markers for retinitis pigmentosa.

Wang DY, Chan WM, Tam PO, Chiang SW, Lam DS, Chong KK, Pang CP.

Hong Kong Med J. 2005 Aug;11(4):281-8. Review.

PMID:
16085945
[PubMed - indexed for MEDLINE]
Free Article
8.

A novel missense RP1 mutation in retinitis pigmentosa.

Chiang SW, Wang DY, Chan WM, Tam PO, Chong KK, Lam DS, Pang CP.

Eye (Lond). 2006 May;20(5):602-5. Review.

PMID:
15933747
[PubMed - indexed for MEDLINE]
9.

Molecular genetics of retinitis pigmentosa.

Farber DB, Heckenlively JR, Sparkes RS, Bateman JB.

West J Med. 1991 Oct;155(4):388-99. Review.

PMID:
1771877
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

[Complicated cataracts in various forms of retinitis pigmentosa. Type and incidence].

Auffarth GU, Tetz MR, Krastel H, Blankenagel A, Völcker HE.

Ophthalmologe. 1997 Sep;94(9):642-6. Review. German.

PMID:
9410231
[PubMed - indexed for MEDLINE]
11.

Epidemiology of retinitis pigmentosa in the Valencian community (Spain).

Nájera C, Millán JM, Beneyto M, Prieto F.

Genet Epidemiol. 1995;12(1):37-46. Review.

PMID:
7713399
[PubMed - indexed for MEDLINE]
12.

Retinitis pigmentosa: genes, proteins and prospects.

Hims MM, Diager SP, Inglehearn CF.

Dev Ophthalmol. 2003;37:109-25. Review.

PMID:
12876833
[PubMed - indexed for MEDLINE]
13.

RCC1-like domain and ORF15: essentials in RPGR gene.

Jin ZB, Hayakawa M, Murakami A, Nao-i N.

Adv Exp Med Biol. 2006;572:29-33. Review.

PMID:
17249551
[PubMed - indexed for MEDLINE]
14.

[Early therapeutic trials for retinitis pigmentosa].

Dufier JL.

Bull Acad Natl Med. 2003;187(9):1685-92; discussion 1692-4. Review. French.

PMID:
15369238
[PubMed - indexed for MEDLINE]
15.

[Genetics of retinitis pigmentosa: metabolic classification and phenotype/genotype correlations].

Maubaret C, Hamel C.

J Fr Ophtalmol. 2005 Jan;28(1):71-92. Review. French.

PMID:
15767903
[PubMed - indexed for MEDLINE]
Free Article
16.

[Genetic heterogeneity of retinitis pigmentosa].

Krawczyński MR, Pecold K.

Klin Oczna. 1994 Jan;96(1):24-9. Review. Polish.

PMID:
8078270
[PubMed - indexed for MEDLINE]
17.

[Retinitis pigmentosa--clinical, genetic and pathophysiologic aspects].

Jurklies B, Zrenner E, Wessing A.

Klin Monbl Augenheilkd. 1997 Jan;210(1):1-18. Review. German.

PMID:
9206727
[PubMed - indexed for MEDLINE]
18.

Molecular genetics of human retinal dystrophies.

Inglehearn CF.

Eye (Lond). 1998;12 ( Pt 3b):571-9. Review.

PMID:
9775219
[PubMed - indexed for MEDLINE]
19.

Hereditary retinitis pigmentosa: recent findings from electroretinography, fundus reflectometry, and psychophysics.

Sandberg MA.

Int Ophthalmol Clin. 1980 Spring;20(1):39-52. Review. No abstract available.

PMID:
6995379
[PubMed - indexed for MEDLINE]
20.

Towards understanding CRUMBS function in retinal dystrophies.

Richard M, Roepman R, Aartsen WM, van Rossum AG, den Hollander AI, Knust E, Wijnholds J, Cremers FP.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R235-43. Review.

PMID:
16987889
[PubMed - indexed for MEDLINE]
Free Article

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