These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 11811080)

  • 21. [Bilateral progressive optic atrophy and without diabetic retinopathy in a young diabetic patient. Wolfram syndrome: diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD)].
    Meyer CH; Rodrigues EB; Schmidt JC
    Ophthalmologe; 2004 Apr; 101(4):394-6. PubMed ID: 15067422
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. Wolfram Syndrome. Case report.
    Tarała W; Drachal E; Mazur A; Korczowski B; Szadkowska A; Zmysłowska A; Młynarski W
    Pediatr Endocrinol Diabetes Metab; 2016; 22(1):39-42. PubMed ID: 28132072
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Primary diagnosis of Wolfram syndrome in an adult patient--case report and description of a novel pathogenic mutation.
    Waschbisch A; Volbers B; Struffert T; Hoyer J; Schwab S; Bardutzky J
    J Neurol Sci; 2011 Jan; 300(1-2):191-3. PubMed ID: 20875904
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study.
    d'Annunzio G; Minuto N; D'Amato E; de Toni T; Lombardo F; Pasquali L; Lorini R
    Diabetes Care; 2008 Sep; 31(9):1743-5. PubMed ID: 18566338
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Optic atrophy as a sign of wolfram syndrome.
    Dedes W; Wildberger H; Landau K
    Klin Monbl Augenheilkd; 2005 Mar; 222(3):248-51. PubMed ID: 15785992
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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
    J Pediatr Endocrinol Metab; 2011; 24(5-6):389-91. PubMed ID: 21823543
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [DIDMOAD syndrome].
    Alicanoğlu R; Canbakan B; Yildiz N; Arikan E; Kundur H; Bahtiyar K; Sayali E
    Wien Med Wochenschr; 1994; 144(4):78-81. PubMed ID: 8023526
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [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]  

  • 32. Identification of a novel WFS1 mutation (AFF344-345ins) in Japanese patients with Wolfram syndrome.
    Inukai K; Awata T; Inoue K; Kurihara S; Nakashima Y; Watanabe M; Sawa T; Takata N; Katayama S
    Diabetes Res Clin Pract; 2005 Aug; 69(2):136-41. PubMed ID: 16005363
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. [Wolfram syndrome. A new case report].
    Bouslama K; Naoui A; Rezgui L; Goucha S; M'Rad S; Ben Dridi M
    Tunis Med; 2002 Nov; 80(11):714-7. PubMed ID: 12664522
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13.
    Acharya A; Raza SI; Anwar MZ; Bharadwaj T; Liaqat K; Khokhar MAS; Everard JL; Nasir A; ; Nickerson DA; Bamshad MJ; Ansar M; Schrauwen I; Ahmad W; Leal SM
    J Hum Genet; 2021 Oct; 66(10):1009-1018. PubMed ID: 33879837
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. [Positional cloning of the gene(WFS1) for Wolfram syndrome].
    Tanizawa Y; Inoue H; Oka Y
    Rinsho Byori; 2000 Oct; 48(10):941-7. PubMed ID: 11215108
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Two cases of Wolfram syndrome].
    Sayouti A; Benhaddou R; Khoumiri R; Gaboune L; Guelzim H; Benfdil N; Moutaoukil A
    J Fr Ophtalmol; 2007 Jun; 30(6):607-9. PubMed ID: 17646750
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 9.