Similar articles for PMID: 25282462

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1969	1
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1

Bessahraoui M, Paquis V, Rouzier C, Bouziane-Nedjadi K, Naceur M, Niar S, Zennaki A, Boudraa G, Touhami M. Bessahraoui M, et al. Arch Pediatr. 2014 Nov;21(11):1229-32. doi: 10.1016/j.arcped.2014.08.017. Epub 2014 Oct 2. Arch Pediatr. 2014. PMID: 25282462 French.

2

A single base-pair deletion in the WFS1 gene causes Wolfram syndrome.

Pitt K, James C, Kochar IS, Kapoor A, Jain S, Hussain K, Bennett K. Pitt K, et al. J Pediatr Endocrinol Metab. 2011;24(5-6):389-91. doi: 10.1515/jpem.2011.215. J Pediatr Endocrinol Metab. 2011. PMID: 21823543

3

Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro).

Yuca SA, Rendtorff ND, Boulahbel H, Lodahl M, Tranebjærg L, Cesur Y, Dogan M, Yilmaz C, Akgun C, Acikgoz M. Yuca SA, et al. Eur J Med Genet. 2012 Jan;55(1):37-42. doi: 10.1016/j.ejmg.2011.08.005. Epub 2011 Sep 23. Eur J Med Genet. 2012. PMID: 21968327

4

c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.

Safarpour Lima B, Ghaedi H, Daftarian N, Ahmadieh H, Jamshidi J, Khorrami M, Noroozi R, Sohrabifar N, Assarzadegan F, Hesami O, Taghavi S, Ahmadifard A, Atakhorrami M, Rahimi-Aliabadi S, Shahmohammadibeni N, Alehabib E, Andarva M, Darvish H, Emamalizadeh B. Safarpour Lima B, et al. Eur J Med Genet. 2016 Feb;59(2):65-9. doi: 10.1016/j.ejmg.2016.01.001. Epub 2016 Jan 7. Eur J Med Genet. 2016. PMID: 26773575

5

Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms.

Sobhani M, Tabatabaiefar MA, Rajab A, Kajbafzadeh AM, Noori-Daloii MR. Sobhani M, et al. Gene. 2013 Oct 10;528(2):309-13. doi: 10.1016/j.gene.2013.06.040. Epub 2013 Jul 8. Gene. 2013. PMID: 23845777

6

[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. Pennings RJ, et al. Ned Tijdschr Geneeskd. 2002 May 25;146(21):985-7. Ned Tijdschr Geneeskd. 2002. PMID: 12058630 Review. Dutch.

7

Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?

Ghirardello S, Dusi E, Castiglione B, Fumagalli M, Mosca F. Ghirardello S, et al. Ital J Pediatr. 2014 Sep 26;40:76. doi: 10.1186/s13052-014-0076-4. Ital J Pediatr. 2014. PMID: 25255707 Free PMC article.

8

First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene.

Domènech E, Kruyer H, Gómez C, Calvo MT, Nunes V. Domènech E, et al. Prenat Diagn. 2004 Oct;24(10):787-9. doi: 10.1002/pd.982. Prenat Diagn. 2004. PMID: 15503287

9

Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.

Gómez-Zaera M, Strom TM, Rodríguez B, Estivill X, Meitinger T, Nunes V. Gómez-Zaera M, et al. Mol Genet Metab. 2001 Jan;72(1):72-81. doi: 10.1006/mgme.2000.3107. Mol Genet Metab. 2001. PMID: 11161832

10

[Wolfram syndrome: clinical and genetic analysis in two sisters].

Conart JB, Maalouf T, Jonveaux P, Guerci B, Angioi K. Conart JB, et al. J Fr Ophtalmol. 2011 Oct;34(8):543-6. doi: 10.1016/j.jfo.2011.02.014. Epub 2011 May 31. J Fr Ophtalmol. 2011. PMID: 21632151 French.

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