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Journal Abstract Search

120 related items for PubMed ID: 15852062

  • 1. Wolframin mutations and hospitalization for psychiatric illness.
    Swift M, Swift RG.
    Mol Psychiatry; 2005 Aug; 10(8):799-803. PubMed ID: 15852062
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Predisposition of Wolfram syndrome heterozygotes to psychiatric illness.
    Swift RG, Polymeropoulos MH, Torres R, Swift M.
    Mol Psychiatry; 1998 Jan; 3(1):86-91. PubMed ID: 9491819
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Molecular detection of novel WFS1 mutations in patients with Wolfram syndrome by a DHPLC-based assay.
    Colosimo A, Guida V, Rigoli L, Di Bella C, De Luca A, Briuglia S, Stuppia L, Salpietro DC, Dallapiccola B.
    Hum Mutat; 2003 Jun; 21(6):622-9. PubMed ID: 12754709
    [Abstract] [Full Text] [Related]

  • 6. Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified.
    Hansen L, Eiberg H, Barrett T, Bek T, Kjaersgaard P, Tranebjaerg L, Rosenberg T.
    Eur J Hum Genet; 2005 Dec; 13(12):1275-84. PubMed ID: 16151413
    [Abstract] [Full Text] [Related]

  • 7. Psychiatric disorders in 36 families with Wolfram syndrome.
    Swift RG, Perkins DO, Chase CL, Sadler DB, Swift M.
    Am J Psychiatry; 1991 Jun; 148(6):775-9. PubMed ID: 2035720
    [Abstract] [Full Text] [Related]

  • 8. Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.
    Giuliano F, Bannwarth S, Monnot S, Cano A, Chabrol B, Vialettes B, Delobel B, Paquis-Flucklinger V, French Group of WS.
    Hum Mutat; 2005 Jan; 25(1):99-100. PubMed ID: 15605410
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

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  • 11. Novel mutations of wolframin: a report with a look at the protein structure.
    Alimadadi A, Ebrahim-Habibi A, Abbasi F, Amoli M, Sayahpour FA, Larijani B.
    Clin Genet; 2011 Jan; 79(1):96-9. PubMed ID: 21143470
    [No Abstract] [Full Text] [Related]

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  • 13. Study of the WFS1 gene and mitochondrial DNA in Spanish Wolfram syndrome families.
    Domènech E, Gómez-Zaera M, Nunes V.
    Clin Genet; 2004 Jun; 65(6):463-9. PubMed ID: 15151504
    [Abstract] [Full Text] [Related]

  • 14. [Research progress of mutational spectrum and pathophysiology of WFS1 gene in Wolfram syndrome and nonsyndromic low frequency sensorineural hearing loss].
    Shi SM, Han YH, Wang HB.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Sep 07; 51(9):712-715. PubMed ID: 27666717
    [Abstract] [Full Text] [Related]

  • 15. Psychiatric disorders and mutations at the Wolfram syndrome locus.
    Swift M, Swift RG.
    Biol Psychiatry; 2000 May 01; 47(9):787-93. PubMed ID: 10812037
    [Abstract] [Full Text] [Related]

  • 16. Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4.
    Polymeropoulos MH, Swift RG, Swift M.
    Nat Genet; 1994 Sep 01; 8(1):95-7. PubMed ID: 7987399
    [Abstract] [Full Text] [Related]

  • 17. Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism.
    Laurier V, Stoetzel C, Muller J, Thibault C, Corbani S, Jalkh N, Salem N, Chouery E, Poch O, Licaire S, Danse JM, Amati-Bonneau P, Bonneau D, Mégarbané A, Mandel JL, Dollfus H.
    Eur J Hum Genet; 2006 Nov 01; 14(11):1195-203. PubMed ID: 16823392
    [Abstract] [Full Text] [Related]

  • 18. WFS1 mutations in Spanish patients with diabetes mellitus and deafness.
    Domènech E, Gómez-Zaera M, Nunes V.
    Eur J Hum Genet; 2002 Jul 01; 10(7):421-6. PubMed ID: 12107816
    [Abstract] [Full Text] [Related]

  • 19. WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.
    Zalloua PA, Azar ST, Delépine M, Makhoul NJ, Blanc H, Sanyoura M, Lavergne A, Stankov K, Lemainque A, Baz P, Julier C.
    Hum Mol Genet; 2008 Dec 15; 17(24):4012-21. PubMed ID: 18806274
    [Abstract] [Full Text] [Related]

  • 20. Cancer risk of heterozygotes with the NBN founder mutation.
    Seemanová E, Jarolim P, Seeman P, Varon R, Digweed M, Swift M, Sperling K.
    J Natl Cancer Inst; 2007 Dec 19; 99(24):1875-80. PubMed ID: 18073374
    [Abstract] [Full Text] [Related]

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