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Related Articles by Review for PubMed (Select 11709537)

1.

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM.

Hum Mol Genet. 2001 Oct 15;10(22):2501-8.

2.

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
3.

[From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)].

Pennings RJ, Cryns K, Huygen PL, van Camp G, Cremers CW.

Ned Tijdschr Geneeskd. 2003 Nov 1;147(44):2170-2. Review. Dutch.

PMID:
14626834
4.

WFS1-Related Disorders.

Tranebjærg L, Barrett T, Rendtorff ND.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2009 Feb 24 [updated 2013 Dec 19].

5.

[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
6.

[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
7.

Hereditary deafness and phenotyping in humans.

Bitner-Glindzicz M.

Br Med Bull. 2002;63:73-94. Review.

PMID:
12324385
8.

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
9.

TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness.

Guipponi M, Antonarakis SE, Scott HS.

Front Biosci. 2008 Jan 1;13:1557-67. Review.

PMID:
17981648
11.

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
12.

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
13.

Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping.

Chen AH, Mueller RF, Prasad SD, Greinwald JH Jr, Manaligod J, Muilenburg AC, Verhoeven K, Van Camp G, Smith RJ.

Arch Otolaryngol Head Neck Surg. 1998 Jan;124(1):20-4. Review.

PMID:
9440775
14.

[Genetic aspects of deafness].

Dallapiccola B, Mingarelli R, Gennarelli M, Novelli G.

Acta Otorhinolaryngol Ital. 1996 Apr;16(2):79-90. Review. Italian.

PMID:
8766069
15.

Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes.

Stinckens C, Ensink R, Feenstra L, Fryns JP, Cremers C.

Int J Pediatr Otorhinolaryngol. 1997 Jan 3;38(3):237-45. Review.

PMID:
9051428
16.

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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19.

Wolfram (DIDMOAD) syndrome.

Barrett TG, Bundey SE.

J Med Genet. 1997 Oct;34(10):838-41. Review.

20.

Psychiatric disorders and mutations at the Wolfram syndrome locus.

Swift M, Swift RG.

Biol Psychiatry. 2000 May 1;47(9):787-93. Review.

PMID:
10812037
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