206 related articles for article (PubMed ID: 25210753)
1. Three cases of Wolfram syndrome with different clinical aspects.
Çamtosun E; Şıklar Z; Kocaay P; Ceylaner S; Flanagan SE; Ellard S; Berberoğlu M
J Pediatr Endocrinol Metab; 2015 Mar; 28(3-4):433-8. PubMed ID: 25210753
[TBL] [Abstract][Full Text] [Related]
2. Wolfram syndrome 1 and Wolfram syndrome 2.
Rigoli L; Di Bella C
Curr Opin Pediatr; 2012 Aug; 24(4):512-7. PubMed ID: 22790102
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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
Ital J Pediatr; 2014 Sep; 40():76. PubMed ID: 25255707
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report.
Sahli M; Zrhidri A; Boualaoui I; Cherkaoui Jaouad I; El Kadiri Y; Nouini Y; Sefiani A
J Med Case Rep; 2023 Sep; 17(1):409. PubMed ID: 37752530
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Identification of a missense variant in the WFS1 gene that causes a mild form of Wolfram syndrome and is associated with risk for type 2 diabetes in Ashkenazi Jewish individuals.
Bansal V; Boehm BO; Darvasi A
Diabetologia; 2018 Oct; 61(10):2180-2188. PubMed ID: 30014265
[TBL] [Abstract][Full Text] [Related]
9. [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; 146(21):985-7. PubMed ID: 12058630
[TBL] [Abstract][Full Text] [Related]
10. Novel missense
Mair H; Fowler N; Papatzanaki ME; Sudhakar P; Maldonado RS
Ophthalmic Genet; 2022 Aug; 43(4):567-572. PubMed ID: 35450504
[TBL] [Abstract][Full Text] [Related]
11. Wolfram Syndrome: a rare optic neuropathy in youth with type 1 diabetes.
Bucca BC; Klingensmith G; Bennett JL
Optom Vis Sci; 2011 Nov; 88(11):E1383-90. PubMed ID: 21892113
[TBL] [Abstract][Full Text] [Related]
12. Genotypic classification of patients with Wolfram syndrome: insights into the natural history of the disease and correlation with phenotype.
de Heredia ML; Clèries R; Nunes V
Genet Med; 2013 Jul; 15(7):497-506. PubMed ID: 23429432
[TBL] [Abstract][Full Text] [Related]
13. Multidimensional analysis and therapeutic development using patient iPSC-derived disease models of Wolfram syndrome.
Kitamura RA; Maxwell KG; Ye W; Kries K; Brown CM; Augsornworawat P; Hirsch Y; Johansson MM; Weiden T; Ekstein J; Cohen J; Klee J; Leslie K; Simeonov A; Henderson MJ; Millman JR; Urano F
JCI Insight; 2022 Sep; 7(18):. PubMed ID: 36134655
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 29774890
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Segregation of two variants suggests the presence of autosomal dominant and recessive forms of
Lusk L; Black E; Vengoechea J
J Med Genet; 2020 Feb; 57(2):121-123. PubMed ID: 31363008
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prevalence and phenotypic features of diabetes due to recessive, non-syndromic WFS1 mutations.
Zhu M; Li Y; Dong G; Chen X; Huang K; Wu W; Dai Y; Zhang L; Lin H; Wang S; Polychronakos C; Fu J
Eur J Endocrinol; 2021 Dec; 186(2):163-170. PubMed ID: 34792487
[TBL] [Abstract][Full Text] [Related]
19. Delineating Wolfram-like syndrome: A systematic review and discussion of the WFS1-associated disease spectrum.
de Muijnck C; Brink JBT; Bergen AA; Boon CJF; van Genderen MM
Surv Ophthalmol; 2023; 68(4):641-654. PubMed ID: 36764396
[TBL] [Abstract][Full Text] [Related]
20. Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.
Sobhani M; Tabatabaiefar MA; Ghafouri-Fard S; Rajab A; Hojjat A; Kajbafzadeh AM; Noori-Daloii MR
BMC Med Genet; 2020 Jan; 21(1):13. PubMed ID: 31937257
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
