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Items: 20

1.

Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene product.

Hofmann S, Philbrook C, Gerbitz KD, Bauer MF.

Hum Mol Genet. 2003 Aug 15;12(16):2003-12.

PMID:
12913071
2.

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
3.

[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
4.

[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.

5.

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
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.

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
8.

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
9.

Current developments in Wolfram syndrome.

Ganie MA, Bhat D.

J Pediatr Endocrinol Metab. 2009 Jan;22(1):3-10. Review.

PMID:
19344068
10.

[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
11.

Reflexions on a newly discovered diabetogenic gene, wolframin (WFS1).

Gerbitz KD.

Diabetologia. 1999 May;42(5):627-30. Review. No abstract available.

PMID:
10333058
12.

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
13.

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
14.

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
15.

Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease.

Rigoli L, Bramanti P, Di Bella C, De Luca F.

Pediatr Res. 2018 May;83(5):921-929. doi: 10.1038/pr.2018.17. Epub 2018 Feb 28. Review.

PMID:
29774890
16.

[Wolfram syndrome].

Oka Y.

Nihon Rinsho. 2006 Sep 28;Suppl 3:138-42. Review. Japanese. No abstract available.

PMID:
17022518
17.

[Wolfram syndrome].

Oka Y.

Nihon Rinsho. 2002 Sep;60 Suppl 9:846-8. Review. Japanese. No abstract available.

PMID:
12387095
18.

Wolfram syndrome.

Minton JA, Rainbow LA, Ricketts C, Barrett TG.

Rev Endocr Metab Disord. 2003 Mar;4(1):53-9. Review. No abstract available.

PMID:
12618560
19.

[Wolfram syndrome. Report of 3 cases].

Benchekroun A, Nouini Y, Iken A, Iraqui M, el Alj HA, Jdoud CO.

Prog Urol. 2001 Dec;11(6):1292-7. Review. French.

PMID:
11859669
20.

[Diabetes (insipidus/mellitus)-optic atrophy-deafness].

Yokoyama Y.

Ryoikibetsu Shokogun Shirizu. 2001;(33):553-4. Review. Japanese. No abstract available.

PMID:
11462565

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