BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 related articles for article (PubMed ID: 19344068)

  • 1. Current developments in Wolfram syndrome.
    Ganie MA; Bhat D
    J Pediatr Endocrinol Metab; 2009 Jan; 22(1):3-10. PubMed ID: 19344068
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Wolfram (DIDMOAD) syndrome.
    Barrett TG; Bundey SE
    J Med Genet; 1997 Oct; 34(10):838-41. PubMed ID: 9350817
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [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]  

  • 5. 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]  

  • 6. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.
    Barrett TG; Bundey SE; Macleod AF
    Lancet; 1995 Dec; 346(8988):1458-63. PubMed ID: 7490992
    [TBL] [Abstract][Full Text] [Related]  

  • 7. False diagnosis of type 1 diabetes mellitus and its complications in Wolfram syndrome--is it the reason for the low number of reported cases of this abnormality?
    Homa K; Stefański A; Zmysłowska A; Molęda P; Bryśkiewicz ME; Majkowska L
    Endokrynol Pol; 2014; 65(5):398-400. PubMed ID: 25301491
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. 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]  

  • 10. The subtle signs of Wolfram (DIDMOAD) syndrome: not all juvenile diabetes is type 1 diabetes.
    Boettcher C; Brosig B; Zimmer KP; Wudy SA
    J Pediatr Endocrinol Metab; 2011; 24(1-2):71-4. PubMed ID: 21528819
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 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. 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]  

    [Next]    [New Search]
    of 12.