BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

279 related articles for article (PubMed ID: 21892113)

  • 21. 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]  

  • 22. [Wolfram syndrome. Three case reports].
    Hajji Z; Halhal M; Chaoui Z; Chefchaouni M; Agnaou L; Berraho A
    J Fr Ophtalmol; 1998 Dec; 21(10):734-40. PubMed ID: 10052046
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Wolfram syndrome and WFS1 gene.
    Rigoli L; Lombardo F; Di Bella C
    Clin Genet; 2011 Feb; 79(2):103-17. PubMed ID: 20738327
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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]  

  • 27. [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]  

  • 28. 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]  

  • 29. Ophthalmologic findings in fifteen patients with Wolfram syndrome.
    Al-Till M; Jarrah NS; Ajlouni KM
    Eur J Ophthalmol; 2002; 12(2):84-8. PubMed ID: 12022290
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. [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]  

  • 32. [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]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. [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]  

  • 37. Optic atrophy in Wolfram (DIDMOAD) syndrome.
    Barrett TG; Bundey SE; Fielder AR; Good PA
    Eye (Lond); 1997; 11 ( Pt 6)():882-8. PubMed ID: 9537152
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis.
    Awata T; Inoue K; Kurihara S; Ohkubo T; Inoue I; Abe T; Takino H; Kanazawa Y; Katayama S
    Biochem Biophys Res Commun; 2000 Feb; 268(2):612-6. PubMed ID: 10679252
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. A novel compound heterozygous mutation in an adolescent with insulin-dependent diabetes: The challenge of characterizing Wolfram syndrome.
    Maltoni G; Minardi R; Cristalli CP; Nardi L; D'Alberton F; Mantovani V; Zucchini S
    Diabetes Res Clin Pract; 2016 Nov; 121():59-61. PubMed ID: 27657458
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.