394 related articles for article (PubMed ID: 15605410)
1. Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.
Giuliano F; Bannwarth S; Monnot S; Cano A; Chabrol B; Vialettes B; Delobel B; Paquis-Flucklinger V;
Hum Mutat; 2005 Jan; 25(1):99-100. PubMed ID: 15605410
[TBL] [Abstract][Full Text] [Related]
2. Molecular detection of novel WFS1 mutations in patients with Wolfram syndrome by a DHPLC-based assay.
Colosimo A; Guida V; Rigoli L; Di Bella C; De Luca A; Briuglia S; Stuppia L; Salpietro DC; Dallapiccola B
Hum Mutat; 2003 Jun; 21(6):622-9. PubMed ID: 12754709
[TBL] [Abstract][Full Text] [Related]
3. Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.
Gómez-Zaera M; Strom TM; Rodríguez B; Estivill X; Meitinger T; Nunes V
Mol Genet Metab; 2001 Jan; 72(1):72-81. PubMed ID: 11161832
[TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified.
Hansen L; Eiberg H; Barrett T; Bek T; Kjaersgaard P; Tranebjaerg L; Rosenberg T
Eur J Hum Genet; 2005 Dec; 13(12):1275-84. PubMed ID: 16151413
[TBL] [Abstract][Full Text] [Related]
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
Gene; 2013 Oct; 528(2):309-13. PubMed ID: 23845777
[TBL] [Abstract][Full Text] [Related]
6. WFS1/wolframin mutations, Wolfram syndrome, and associated diseases.
Khanim F; Kirk J; Latif F; Barrett TG
Hum Mutat; 2001 May; 17(5):357-67. PubMed ID: 11317350
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 12955714
[TBL] [Abstract][Full Text] [Related]
8. WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.
Zalloua PA; Azar ST; Delépine M; Makhoul NJ; Blanc H; Sanyoura M; Lavergne A; Stankov K; Lemainque A; Baz P; Julier C
Hum Mol Genet; 2008 Dec; 17(24):4012-21. PubMed ID: 18806274
[TBL] [Abstract][Full Text] [Related]
9. Study of the WFS1 gene and mitochondrial DNA in Spanish Wolfram syndrome families.
Domènech E; Gómez-Zaera M; Nunes V
Clin Genet; 2004 Jun; 65(6):463-9. PubMed ID: 15151504
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome.
Gasparin MR; Crispim F; Paula SL; Freire MB; Dalbosco IS; Manna TD; Salles JE; Gasparin F; Guedes A; Marcantonio JM; Gambini M; Salim CP; Moisés RS
Eur J Endocrinol; 2009 Feb; 160(2):309-16. PubMed ID: 19042979
[TBL] [Abstract][Full Text] [Related]
12. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Identification of novel WFS1 mutations in Italian children with Wolfram syndrome.
Tessa A; Carbone I; Matteoli MC; Bruno C; Patrono C; Patera IP; De Luca F; Lorini R; Santorelli FM
Hum Mutat; 2001 Apr; 17(4):348-9. PubMed ID: 11295831
[TBL] [Abstract][Full Text] [Related]
15. WFS1 mutations in Spanish patients with diabetes mellitus and deafness.
Domènech E; Gómez-Zaera M; Nunes V
Eur J Hum Genet; 2002 Jul; 10(7):421-6. PubMed ID: 12107816
[TBL] [Abstract][Full Text] [Related]
16. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome).
Inoue H; Tanizawa Y; Wasson J; Behn P; Kalidas K; Bernal-Mizrachi E; Mueckler M; Marshall H; Donis-Keller H; Crock P; Rogers D; Mikuni M; Kumashiro H; Higashi K; Sobue G; Oka Y; Permutt MA
Nat Genet; 1998 Oct; 20(2):143-8. PubMed ID: 9771706
[TBL] [Abstract][Full Text] [Related]
17. Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1.
Hardy C; Khanim F; Torres R; Scott-Brown M; Seller A; Poulton J; Collier D; Kirk J; Polymeropoulos M; Latif F; Barrett T
Am J Hum Genet; 1999 Nov; 65(5):1279-90. PubMed ID: 10521293
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation of WFS1 gene in a Japanese man of Wolfram syndrome with positive diabetes-related antibodies.
Nakamura A; Shimizu C; Nagai S; Taniguchi S; Umetsu M; Atsumi T; Wada N; Yoshioka N; Ono Y; Tanizawa Y; Koike T
Diabetes Res Clin Pract; 2006 Aug; 73(2):215-7. PubMed ID: 16442662
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutations.
Pennings RJ; Huygen PL; van den Ouweland JM; Cryns K; Dikkeschei LD; Van Camp G; Cremers CW
Audiol Neurootol; 2004; 9(1):51-62. PubMed ID: 14676474
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
