Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 25

1.
2.

[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
3.

ABCR unites what ophthalmologists divide(s)

van Driel MA, Maugeri A, Klevering BJ, Hoyng CB, Cremers FP.

Ophthalmic Genet. 1998 Sep;19(3):117-22. Review.

PMID:
9810566
4.

The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial.

Shroyer NF, Lewis RA, Allikmets R, Singh N, Dean M, Leppert M, Lupski JR.

Vision Res. 1999 Jul;39(15):2537-44. Review.

5.

Stargardt's disease and the ABCR gene.

Westerfeld C, Mukai S.

Semin Ophthalmol. 2008 Jan-Feb;23(1):59-65. doi: 10.1080/08820530701745249. Review.

PMID:
18214793
6.

Cone rod dystrophies.

Hamel CP.

Orphanet J Rare Dis. 2007 Feb 1;2:7. Review.

7.

The gene for Stargardt disease, ABCA4, is a major retinal gene: a mini-review.

Koenekoop RK.

Ophthalmic Genet. 2003 Jun;24(2):75-80. Review. Erratum in: Ophthalmic Genet. 2003 Dec;24(4):253.

PMID:
12789571
8.

[Early therapeutic trials for retinitis pigmentosa].

Dufier JL.

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

PMID:
15369238
9.

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
10.
11.

[Genetic heterogeneity of retinitis pigmentosa].

KrawczyƄski MR, Pecold K.

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

PMID:
8078270
12.

[Retinal involvement and genetic myopathy].

Sacconi S, Baillif-Gostoli S, Desnuelle C.

Rev Neurol (Paris). 2010 Dec;166(12):998-1009. doi: 10.1016/j.neurol.2010.09.001. Epub 2010 Nov 10. Review. French.

PMID:
21071050
13.

Stargardt-Fundus flavimaculatus: recent advancements and treatment.

Haji Abdollahi S, Hirose T.

Semin Ophthalmol. 2013 Sep-Nov;28(5-6):372-6. doi: 10.3109/08820538.2013.825286. Review.

PMID:
24138045
14.

Molecular genetics of human retinal dystrophies.

Inglehearn CF.

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

PMID:
9775219
15.
16.

The ABCR gene: a major disease gene in macular and peripheral retinal degenerations with onset from early childhood to the elderly.

Rozet JM, Gerber S, Souied E, Ducroq D, Perrault I, Ghazi I, Soubrane G, Coscas G, Dufier JL, Munnich A, Kaplan J.

Mol Genet Metab. 1999 Oct;68(2):310-5. Review. No abstract available.

PMID:
10527682
17.

[Current advances in gene diagnosis and therapy of gelatinous drop-like corneal dystrophy].

Huo YN, Yao YF.

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2006 Mar;35(2):228-32. Review. Chinese.

PMID:
16610095
18.

Allelic and phenotypic heterogeneity in ABCA4 mutations.

Burke TR, Tsang SH.

Ophthalmic Genet. 2011 Sep;32(3):165-74. doi: 10.3109/13816810.2011.565397. Epub 2011 Apr 21. Review.

19.

Genetic heterogeneity of Usher syndrome.

Kimberling WJ, Orten D, Pieke-Dahl S.

Adv Otorhinolaryngol. 2000;56:11-8. Review.

PMID:
10868209
20.

Ocular manifestations of metabolic disorders.

Iwata F, Kaiser-Kupfer MI.

Curr Opin Ophthalmol. 1995 Dec;6(6):77-81. Review.

PMID:
10160423

Supplemental Content

Support Center