136 related articles for article (PubMed ID: 26829729)
1. [Mutation analysis of 35 Wilson's disease pedigrees].
Zong Y; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):30-3. PubMed ID: 26829729
[TBL] [Abstract][Full Text] [Related]
2. Analysis and application of ATP7B gene mutations in 35 patients with hepatolenticular degeneration.
Zong YN; Kong XD
Genet Mol Res; 2015 Dec; 14(4):18764-70. PubMed ID: 26782526
[TBL] [Abstract][Full Text] [Related]
3. [Genotype and phenotype correlation in Chinese patients with Wilson's Disease].
Liu XQ; Zhang YF; Liu TT; Gu XF; Hsiao KJ; Bao KR; Yu LH
Zhonghua Er Ke Za Zhi; 2003 Jan; 41(1):35-8. PubMed ID: 14761325
[TBL] [Abstract][Full Text] [Related]
4. [Mutation screening and prenatal diagnosis of Wilson's disease by denature high performance liquid chromatography].
Du J; Gao B; Li L; Li W; Lu G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):527-30. PubMed ID: 18841564
[TBL] [Abstract][Full Text] [Related]
5. [Mutational analysis of ATP7B gene of hepatolenticular degeneration in Xinjiang region].
Aerziguli A; Li CZ; Hu LH; Lu XB; Sun XF
Zhonghua Gan Zang Bing Za Zhi; 2020 Aug; 28(8):699-702. PubMed ID: 32911910
[No Abstract] [Full Text] [Related]
6. [Genotype-phenotype relationship and genetics study of 115 cases with Wilson's disease].
Xia JK; Ning HF; Luo X; Zeng Y; Chen YB; Kong XD
Zhonghua Gan Zang Bing Za Zhi; 2024 Jun; 32(6):558-562. PubMed ID: 38964899
[No Abstract] [Full Text] [Related]
7. [Haplotype analysis and possible founder effect at the R778L mutation of the ATP7B gene in Korean patients with Wilson's disease].
Bae SH; Kim JW; Seo JK
Korean J Hepatol; 2009 Sep; 15(3):309-19. PubMed ID: 19783880
[TBL] [Abstract][Full Text] [Related]
8. [Rapid detection of common ATP7B mutations in Wilson disease by high resolution melting analysis].
Zhao X; Liu Y; Huang S; Meng Y; Sun M; Yang W; Zhang X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):515-9. PubMed ID: 18841562
[TBL] [Abstract][Full Text] [Related]
9. Molecular analysis and diagnosis in Japanese patients with Wilson's disease.
Shimizu N; Nakazono H; Takeshita Y; Ikeda C; Fujii H; Watanabe A; Yamaguchi Y; Hemmi H; Shimatake H; Aoki T
Pediatr Int; 1999 Aug; 41(4):409-13. PubMed ID: 10453196
[TBL] [Abstract][Full Text] [Related]
10. Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson's disease.
Folhoffer A; Ferenci P; Csak T; Horvath A; Hegedus D; Firneisz G; Osztovits J; Kosa JP; Willheim-Polli C; Szonyi L; Abonyi M; Lakatos PL; Szalay F
Eur J Gastroenterol Hepatol; 2007 Feb; 19(2):105-11. PubMed ID: 17272994
[TBL] [Abstract][Full Text] [Related]
11. [Phenotype and genotype analysis of 55 children patients with Wilson's disease].
Zhou XY; Yin HX; Wang CL; Liu ZF; Zheng BX; Jin Y
Zhonghua Gan Zang Bing Za Zhi; 2020 Jul; 28(7):603-607. PubMed ID: 32791797
[No Abstract] [Full Text] [Related]
12. A genetic study of Wilson's disease in the United Kingdom.
Coffey AJ; Durkie M; Hague S; McLay K; Emmerson J; Lo C; Klaffke S; Joyce CJ; Dhawan A; Hadzic N; Mieli-Vergani G; Kirk R; Elizabeth Allen K; Nicholl D; Wong S; Griffiths W; Smithson S; Giffin N; Taha A; Connolly S; Gillett GT; Tanner S; Bonham J; Sharrack B; Palotie A; Rattray M; Dalton A; Bandmann O
Brain; 2013 May; 136(Pt 5):1476-87. PubMed ID: 23518715
[TBL] [Abstract][Full Text] [Related]
13. Distinct clinical courses according to presenting phenotypes and their correlations to ATP7B mutations in a large Wilson's disease cohort.
Lee BH; Kim JH; Lee SY; Jin HY; Kim KJ; Lee JJ; Park JY; Kim GH; Choi JH; Kim KM; Yoo HW
Liver Int; 2011 Jul; 31(6):831-9. PubMed ID: 21645214
[TBL] [Abstract][Full Text] [Related]
14. Direct sequencing of mutations in the copper-transporting P-type adenosine triphosphate (ATP7B) gene for diagnosis and pathogenesis of Wilson's disease.
Zhang DF; Teng JF
Genet Mol Res; 2016 Sep; 15(3):. PubMed ID: 27706781
[TBL] [Abstract][Full Text] [Related]
15. Clinical and genetic characterization of a large cohort of patients with Wilson's disease in China.
Zhang S; Yang W; Li X; Pei P; Dong T; Yang Y; Zhang J
Transl Neurodegener; 2022 Feb; 11(1):13. PubMed ID: 35220961
[TBL] [Abstract][Full Text] [Related]
16. Wilson's disease in two consecutive generations: the detection of three mutated alleles in the ATP7B gene in two Sardinian families.
Loudianos G; Zappu A; Lepori MB; Incollu S; Dessì V; Mameli E; Garrucciu G; De Virgiliis S; Cao A
Dig Liver Dis; 2013 Apr; 45(4):342-5. PubMed ID: 23219664
[TBL] [Abstract][Full Text] [Related]
17. [Clinical and genetic study of Wilson's disease in affected twins and siblings].
Cheng N; Wang X; Yu X; Zhou Z; Gao M; Rao R; Hu J; Yang R; Han Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Jun; 30(3):261-5. PubMed ID: 23744310
[TBL] [Abstract][Full Text] [Related]
18. Wilson's disease in Southern Brazil: genotype-phenotype correlation and description of two novel mutations in ATP7B gene.
Bem RS; Raskin S; Muzzillo DA; Deguti MM; Cançado EL; Araújo TF; Nakhle MC; Barbosa ER; Munhoz RP; Teive HA
Arq Neuropsiquiatr; 2013 Aug; 71(8):503-7. PubMed ID: 23982005
[TBL] [Abstract][Full Text] [Related]
19. 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
[TBL] [Abstract][Full Text] [Related]
20. Screening for mutations in ATP7B gene using conformation-sensitive gel electrophoresis in a family with Wilson's disease.
Sundaresan S; Eapen CE; Shaji RV; Chandy M; Kurian G; Chandy G
Med Sci Monit; 2007 Mar; 13(3):CS38-40. PubMed ID: 17325640
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]