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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

180 related items for PubMed ID: 10777157

  • 21. Mutation spectrum and polymorphisms in ATP7B identified on direct sequencing of all exons in Chinese Han and Hui ethnic patients with Wilson's disease.
    Gu YH, Kodama H, Du SL, Gu QJ, Sun HJ, Ushijima H.
    Clin Genet; 2003 Dec; 64(6):479-84. PubMed ID: 14986826
    [Abstract] [Full Text] [Related]

  • 22. [The onset of psychiatric disorders and Wilson's disease].
    Benhamla T, Tirouche YD, Abaoub-Germain A, Theodore F.
    Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
    [Abstract] [Full Text] [Related]

  • 23. Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson's disease: a case report.
    Liu G, Ma D, Cheng J, Zhang J, Luo C, Sun Y, Hu P, Wang Y, Jiang T, Xu Z.
    BMC Med Genet; 2018 Apr 12; 19(1):61. PubMed ID: 29649982
    [Abstract] [Full Text] [Related]

  • 24. Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia.
    Tomić A, Dobricić V, Novaković I, Svetel M, Pekmezović T, Kresojević N, Potrebić A, Kostić VS.
    Vojnosanit Pregl; 2013 May 12; 70(5):457-62. PubMed ID: 23789284
    [Abstract] [Full Text] [Related]

  • 25. Neurologic Wilson's disease.
    Lorincz MT.
    Ann N Y Acad Sci; 2010 Jan 12; 1184():173-87. PubMed ID: 20146697
    [Abstract] [Full Text] [Related]

  • 26. Hypoceruloplasminemia-related movement disorder without Kayser-Fleischer rings is different from Wilson disease and not involved in ATP7B mutation.
    Lirong J, Jianjun J, Hua Z, Guoqiang F, Yuhao Z, Xiaoli P, Xiaomin Z, Yuwen Z, Yu M, Jie C, Jihong D, Yueshi M, Zhenyao M, Chunjiu Z.
    Eur J Neurol; 2009 Oct 12; 16(10):1130-7. PubMed ID: 19572946
    [Abstract] [Full Text] [Related]

  • 27. Population screening for Wilson's disease.
    Hahn SH.
    Ann N Y Acad Sci; 2014 May 12; 1315():64-9. PubMed ID: 24731025
    [Abstract] [Full Text] [Related]

  • 28. 4193delC, a common mutation causing Wilson's disease in Saudi Arabia: rapid molecular screening of patients and carriers.
    Majumdar R, Al Jumah M, Fraser M.
    Mol Pathol; 2003 Oct 12; 56(5):302-4. PubMed ID: 14514926
    [Abstract] [Full Text] [Related]

  • 29. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec 12; 118(3-4):539. PubMed ID: 16402213
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene.
    Mameli E, Lepori MB, Chiappe F, Ranucci G, Di Dato F, Iorio R, Loudianos G.
    Gene; 2015 Sep 15; 569(2):276-9. PubMed ID: 26031236
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Novel mutations of the ATP7B gene in Han Chinese families with pre-symptomatic Wilson's disease.
    Yuan ZF, Wu W, Yu YL, Shen J, Mao SS, Gao F, Xia ZZ.
    World J Pediatr; 2015 Aug 15; 11(3):255-60. PubMed ID: 26253413
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Wilson's disease.
    Ferenci P.
    Clin Liver Dis; 1998 Feb 15; 2(1):31-49, v-vi. PubMed ID: 15560044
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.