BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

352 related articles for article (PubMed ID: 24218323)

  • 1. 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]  

  • 2. [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]  

  • 3. 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]  

  • 4. 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]  

  • 5. [Wolfram syndrome: from definition to molecular bases].
    Ribeiro MR; Crispim F; Vendramini MF; Moisés RS
    Arq Bras Endocrinol Metabol; 2006 Oct; 50(5):839-44. PubMed ID: 17160206
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. A new structural rearrangement associated to Wolfram syndrome in a child with a partial phenotype.
    Elli FM; Ghirardello S; Giavoli C; Gangi S; Dioni L; Crippa M; Finelli P; Bergamaschi S; Mosca F; Spada A; Beck-Peccoz P
    Gene; 2012 Nov; 509(1):168-72. PubMed ID: 22771918
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 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. Wolfram/DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative disease.
    Domenech E; Gomez-Zaera M; Nunes V
    Pediatr Endocrinol Rev; 2006 Mar; 3(3):249-57. PubMed ID: 16639390
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Wolfram Syndrome 1: From Genetics to Therapy.
    Rigoli L; Caruso V; Salzano G; Lombardo F
    Int J Environ Res Public Health; 2022 Mar; 19(6):. PubMed ID: 35328914
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. [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]  

  • 17. [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]  

  • 18. 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]  

  • 19. [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]  

  • 20. 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]  

    [Next]    [New Search]
    of 18.