401 related articles for article (PubMed ID: 15070927)
1. Diabetes mellitus and optic atrophy: a study of Wolfram syndrome in the Lebanese population.
Medlej R; Wasson J; Baz P; Azar S; Salti I; Loiselet J; Permutt A; Halaby G
J Clin Endocrinol Metab; 2004 Apr; 89(4):1656-61. PubMed ID: 15070927
[TBL] [Abstract][Full Text] [Related]
2. Wolfram (DIDMOAD) syndrome: a multidisciplinary clinical study in nine Turkish patients and review of the literature.
Simsek E; Simsek T; Tekgül S; Hosal S; Seyrantepe V; Aktan G
Acta Paediatr; 2003; 92(1):55-61. PubMed ID: 12650300
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [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]
5. [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]
6. Association of Wolfram syndrome with Fallot tetralogy in a girl.
Korkmaz HA; Demir K; Hazan F; Yıldız M; Elmas ÖN; Özkan B
Arch Argent Pediatr; 2016 Jun; 114(3):e163-6. PubMed ID: 27164349
[TBL] [Abstract][Full Text] [Related]
7. Wolfram syndrome in a young woman with associated hypergonadotropic hypogonadism - A case report.
Jodoin A; Marchand M; Beltrand J
J Pediatr Endocrinol Metab; 2022 Dec; 35(12):1552-1555. PubMed ID: 36100371
[TBL] [Abstract][Full Text] [Related]
8. Neuropathy in Wolfram syndrome.
Mathis S; Maisonobe T; Neau JP
Eur J Med Genet; 2011; 54(1):73-5. PubMed ID: 20888932
[TBL] [Abstract][Full Text] [Related]
9. Wolfram syndrome: case report and review of the literature.
Ari S; Keklíkçí U; Caça I; Unlü K; Kayabaşi H
Ann Ophthalmol (Skokie); 2007; 39(1):53-5. PubMed ID: 17914206
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 25764693
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. [Wolfram syndrome: clinical and genetic analysis in two sisters].
Conart JB; Maalouf T; Jonveaux P; Guerci B; Angioi K
J Fr Ophtalmol; 2011 Oct; 34(8):543-6. PubMed ID: 21632151
[TBL] [Abstract][Full Text] [Related]
14. Ophthalmic, systemic, and genetic characteristics of patients with Wolfram syndrome.
Ustaoglu M; Onder F; Karapapak M; Taslidere H; Guven D
Eur J Ophthalmol; 2020 Sep; 30(5):1099-1105. PubMed ID: 30957632
[TBL] [Abstract][Full Text] [Related]
15. Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy.
Scolding NJ; Kellar-Wood HF; Shaw C; Shneerson JM; Antoun N
Ann Neurol; 1996 Mar; 39(3):352-60. PubMed ID: 8602754
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Teaching NeuroImages: a neuroendocrine rarity: Wolfram syndrome.
Vale TC; Perpétuo FO
Neurology; 2013 Nov; 81(20):e153. PubMed ID: 24218323
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]