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Items: 12

1.

A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for Wolfram syndrome 2.

Amr S, Heisey C, Zhang M, Xia XJ, Shows KH, Ajlouni K, Pandya A, Satin LS, El-Shanti H, Shiang R.

Am J Hum Genet. 2007 Oct;81(4):673-83. Epub 2007 Aug 20.

2.

Wolfram syndrome 1 and Wolfram syndrome 2.

Rigoli L, Di Bella C.

Curr Opin Pediatr. 2012 Aug;24(4):512-7. doi: 10.1097/MOP.0b013e328354ccdf. Review.

PMID:
22790102
3.

Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.

Cryns K, Sivakumaran TA, Van den Ouweland JM, Pennings RJ, Cremers CW, Flothmann K, Young TL, Smith RJ, Lesperance MM, Van Camp G.

Hum Mutat. 2003 Oct;22(4):275-87. Review.

PMID:
12955714
4.

[Wolfram syndrome: clinical features, molecular genetics of WFS1 gene].

Tanabe K, Matsunaga K, Hatanaka M, Akiyama M, Tanizawa Y.

Nihon Rinsho. 2015 Feb;73(2):341-9. Review. Japanese.

PMID:
25764693
5.

[Genetic diagnosis of diabetes mellitus: Wolfram syndrome--from positional cloning to DNA diagnosis].

Tanizawa Y.

Rinsho Byori. 2003 Jun;51(6):544-9. Review. Japanese.

PMID:
12884741
6.

[Wolfram syndrome: from definition to molecular bases].

Ribeiro MR, Crispim F, Vendramini MF, Mois├ęs RS.

Arq Bras Endocrinol Metabol. 2006 Oct;50(5):839-44. Review. Portuguese.

7.

WFS1/wolframin mutations, Wolfram syndrome, and associated diseases.

Khanim F, Kirk J, Latif F, Barrett TG.

Hum Mutat. 2001 May;17(5):357-67. Review.

PMID:
11317350
8.

WS1 gene mutation analysis of Wolfram syndrome in a Chinese patient and a systematic review of literatures.

Yu G, Yu ML, Wang JF, Gao CR, Chen ZJ.

Endocrine. 2010 Oct;38(2):147-52. doi: 10.1007/s12020-010-9350-4. Epub 2010 Oct 23. Review.

PMID:
20972738
9.

Wolfram syndrome and WFS1 gene.

Rigoli L, Lombardo F, Di Bella C.

Clin Genet. 2011 Feb;79(2):103-17. doi: 10.1111/j.1399-0004.2010.01522.x. Epub 2010 Aug 26. Review.

PMID:
20738327
10.

Wolfram/DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative disease.

Domenech E, Gomez-Zaera M, Nunes V.

Pediatr Endocrinol Rev. 2006 Mar;3(3):249-57. Review.

PMID:
16639390
11.

[From gene to disease; mutations in the WFS1-gene as the cause of juvenile type I diabetes mellitus with optic atrophy (Wolfram syndrome)].

Pennings RJ, Dikkeschei LD, Cremers CW, van den Ouweland JM.

Ned Tijdschr Geneeskd. 2002 May 25;146(21):985-7. Review. Dutch.

PMID:
12058630
12.

Genetics of hearing loss: Allelism and modifier genes produce a phenotypic continuum.

McHugh RK, Friedman RA.

Anat Rec A Discov Mol Cell Evol Biol. 2006 Apr;288(4):370-81. Review.

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