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 *

115 related articles for article (PubMed ID: 9856492)

  • 41. 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]  

  • 42. Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome.
    Papadimitriou DT; Manolakos E; Bothou C; Zoupanos G; Papoulidis I; Orru S; Skarmoutsos F; Delides A; Bakoula C; Papadimitriou A; Urano F
    Diabetes Metab; 2015 Nov; 41(5):433-5. PubMed ID: 26169481
    [No Abstract]   [Full Text] [Related]  

  • 43. 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]  

  • 44. 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]  

  • 45. Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family.
    Komatsu K; Nakamura N; Ghadami M; Matsumoto N; Kishino T; Ohta T; Niikawa N; Yoshiura K
    J Hum Genet; 2002; 47(8):395-9. PubMed ID: 12181639
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [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]  

  • 47. A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment.
    Tsai HT; Wang YP; Chung SF; Lin HC; Ho GM; Shu MT
    BMC Med Genet; 2007 May; 8():26. PubMed ID: 17517145
    [TBL] [Abstract][Full Text] [Related]  

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

  • 49. DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.
    Wajid M; Abbasi AA; Ansar M; Pham TL; Yan K; Haque S; Ahmad W; Leal SM
    Eur J Hum Genet; 2003 Oct; 11(10):812-5. PubMed ID: 14512973
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutations.
    Pennings RJ; Huygen PL; van den Ouweland JM; Cryns K; Dikkeschei LD; Van Camp G; Cremers CW
    Audiol Neurootol; 2004; 9(1):51-62. PubMed ID: 14676474
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.
    Li M; Liu J; Yi H; Xu L; Zhong X; Peng F
    BMC Pediatr; 2018 Mar; 18(1):116. PubMed ID: 29549887
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Selective cognitive and psychiatric manifestations in Wolfram Syndrome.
    Bischoff AN; Reiersen AM; Buttlaire A; Al-Lozi A; Doty T; Marshall BA; Hershey T;
    Orphanet J Rare Dis; 2015 May; 10():66. PubMed ID: 26025012
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. Clinical and molecular genetic analysis of a new mutation in children with Wolfram syndrome: a case report.
    Xu Q; Qu H; Wei S
    Mol Med Rep; 2013 Mar; 7(3):965-8. PubMed ID: 23338790
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation.
    Bonnycastle LL; Chines PS; Hara T; Huyghe JR; Swift AJ; Heikinheimo P; Mahadevan J; Peltonen S; Huopio H; Nuutila P; Narisu N; Goldfeder RL; Stitzel ML; Lu S; Boehnke M; Urano F; Collins FS; Laakso M
    Diabetes; 2013 Nov; 62(11):3943-50. PubMed ID: 23903355
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Wolfram syndrome: clinical and genetic analysis in two sisters].
    Conart JB; Maalouf T; Jonveaux P; Guerci B; Angioi K
    J Fr Ophtalmol; 2011 Oct; 34(8):543-6. PubMed ID: 21632151
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.
    Manolis EN; Yandavi N; Nadol JB; Eavey RD; McKenna M; Rosenbaum S; Khetarpal U; Halpin C; Merchant SN; Duyk GM; MacRae C; Seidman CE; Seidman JG
    Hum Mol Genet; 1996 Jul; 5(7):1047-50. PubMed ID: 8817345
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Wolfram syndrome: report of four new cases and a review of literature.
    Fishman L; Ehrlich RM
    Diabetes Care; 1986; 9(4):405-8. PubMed ID: 3461931
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.