269 related articles for article (PubMed ID: 18194629)
1. [Wolfram syndrome. Clinical and genetic study in two families].
Lou Frances G; Soto de Ruiz S; López-Madrazo Hernández MJ; Macipe Costa R; Rodríguez Rigual M
An Pediatr (Barc); 2008 Jan; 68(1):54-7. PubMed ID: 18194629
[TBL] [Abstract][Full Text] [Related]
2. 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
Gene; 2013 Oct; 528(2):309-13. PubMed ID: 23845777
[TBL] [Abstract][Full Text] [Related]
3. Identification of unsuspected Wolfram syndrome cases through clinical assessment and WFS1 gene screening in type 1 diabetes mellitus patients.
Blanco-Aguirre ME; la Parra DR; Tapia-Garcia H; Gonzalez-Rodriguez J; Welschen D; Arroyo-Yllanes ME; Escudero I; Nuñez-Hernandez JA; Medina-Bravo P; Zenteno JC
Gene; 2015 Jul; 566(1):63-7. PubMed ID: 25895475
[TBL] [Abstract][Full Text] [Related]
4. Current developments in Wolfram syndrome.
Ganie MA; Bhat D
J Pediatr Endocrinol Metab; 2009 Jan; 22(1):3-10. PubMed ID: 19344068
[TBL] [Abstract][Full Text] [Related]
5. Presentation and clinical course of Wolfram (DIDMOAD) syndrome from North India.
Ganie MA; Laway BA; Nisar S; Wani MM; Khurana ML; Ahmad F; Ahmed S; Gupta P; Ali I; Shabir I; Shadan A; Ahmed A; Tufail S
Diabet Med; 2011 Nov; 28(11):1337-42. PubMed ID: 21726277
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.
Li M; Liu J; Yi H; Xu L; Zhong X; Peng F
BMC Pediatr; 2018 Mar; 18(1):116. PubMed ID: 29549887
[TBL] [Abstract][Full Text] [Related]
7. Association of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. The Wolfram or DIDMOAD syndrome.
Najjar SS; Saikaly MG; Zaytoun GM; Abdelnoor A
Arch Dis Child; 1985 Sep; 60(9):823-8. PubMed ID: 4051539
[TBL] [Abstract][Full Text] [Related]
8. 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
Eur J Med Genet; 2012 Jan; 55(1):37-42. PubMed ID: 21968327
[TBL] [Abstract][Full Text] [Related]
9. Molecular characterization of WFS1 in patients with Wolfram syndrome.
van ven Ouweland JM; Cryns K; Pennings RJ; Walraven I; Janssen GM; Maassen JA; Veldhuijzen BF; Arntzenius AB; Lindhout D; Cremers CW; Van Camp G; Dikkeschei LD
J Mol Diagn; 2003 May; 5(2):88-95. PubMed ID: 12707373
[TBL] [Abstract][Full Text] [Related]
10. Wolfram (DIDMOAD) syndrome.
Barrett TG; Bundey SE
J Med Genet; 1997 Oct; 34(10):838-41. PubMed ID: 9350817
[TBL] [Abstract][Full Text] [Related]
11. [Genetic diagnosis of diabetes mellitus: Wolfram syndrome--from positional cloning to DNA diagnosis].
Tanizawa Y
Rinsho Byori; 2003 Jun; 51(6):544-9. PubMed ID: 12884741
[TBL] [Abstract][Full Text] [Related]
12. A new mutation in WFS1 gene (C.1522-1523delTA, Y508fsX421) may be responsible for early appearance of clinical features of Wolfram syndrome and suicidal behaviour.
Aluclu MU; Bahceci M; Tuzcu A; Arikan S; Gokalp D
Neuro Endocrinol Lett; 2006 Dec; 27(6):691-4. PubMed ID: 17187023
[TBL] [Abstract][Full Text] [Related]
13. [Familial Wolfram syndrome].
Bessahraoui M; Paquis V; Rouzier C; Bouziane-Nedjadi K; Naceur M; Niar S; Zennaki A; Boudraa G; Touhami M
Arch Pediatr; 2014 Nov; 21(11):1229-32. PubMed ID: 25282462
[TBL] [Abstract][Full Text] [Related]
14. Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives.
Pallotta MT; Tascini G; Crispoldi R; Orabona C; Mondanelli G; Grohmann U; Esposito S
J Transl Med; 2019 Jul; 17(1):238. PubMed ID: 31337416
[TBL] [Abstract][Full Text] [Related]
15. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.
Barrett TG; Bundey SE; Macleod AF
Lancet; 1995 Dec; 346(8988):1458-63. PubMed ID: 7490992
[TBL] [Abstract][Full Text] [Related]
16. First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene.
Domènech E; Kruyer H; Gómez C; Calvo MT; Nunes V
Prenat Diagn; 2004 Oct; 24(10):787-9. PubMed ID: 15503287
[TBL] [Abstract][Full Text] [Related]
17. The novel compound heterozygous mutations, V434del and W666X, in WFS1 gene causing the Wolfram syndrome in a Chinese family.
Hong J; Zhang YW; Zhang HJ; Jia HY; Zhang Y; Ding XY; Zhou DY; Chen HP; Jiang XH; Cui B; Li XY; Ning G
Endocrine; 2009 Apr; 35(2):151-7. PubMed ID: 19160074
[TBL] [Abstract][Full Text] [Related]
18. Wolfram syndrome in the Japanese population; molecular analysis of WFS1 gene and characterization of clinical features.
Matsunaga K; Tanabe K; Inoue H; Okuya S; Ohta Y; Akiyama M; Taguchi A; Kora Y; Okayama N; Yamada Y; Wada Y; Amemiya S; Sugihara S; Nakao Y; Oka Y; Tanizawa Y
PLoS One; 2014; 9(9):e106906. PubMed ID: 25211237
[TBL] [Abstract][Full Text] [Related]
19. Wolfram syndrome: Portuguese research.
Ferreras C; Gorito V; Pedro J; Ferreira S; Costa C; Santos Silva R; Castro Correia C
Endokrynol Pol; 2021; 72(4):353-356. PubMed ID: 34010437
[TBL] [Abstract][Full Text] [Related]
20. Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A).
Çelmeli G; Türkkahraman D; Çürek Y; Houghton J; Akçurin S; Bircan İ
J Clin Res Pediatr Endocrinol; 2017 Mar; 9(1):80-84. PubMed ID: 27468121
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]