313 related articles for article (PubMed ID: 22221592)
1. Apolipoprotein E gene (APOE) genotype in Wilson's disease: impact on clinical presentation.
Litwin T; Gromadzka G; Członkowska A
Parkinsonism Relat Disord; 2012 May; 18(4):367-9. PubMed ID: 22221592
[TBL] [Abstract][Full Text] [Related]
2. The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson's disease.
Schiefermeier M; Kollegger H; Madl C; Polli C; Oder W; Kühn H; Berr F; Ferenci P
Brain; 2000 Mar; 123 Pt 3():585-90. PubMed ID: 10686180
[TBL] [Abstract][Full Text] [Related]
3. p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease.
Gromadzka G; Schmidt HH; Genschel J; Bochow B; Rodo M; Tarnacka B; Litwin T; Chabik G; Członkowska A
Mov Disord; 2006 Feb; 21(2):245-8. PubMed ID: 16211609
[TBL] [Abstract][Full Text] [Related]
4. Apolipoprotein E genotype analysis in Chinese Han ethnic children with Wilson's disease, with a concentration on those homozygous for R778L.
Gu YH; Kodama H; Du SL
Brain Dev; 2005 Dec; 27(8):551-3. PubMed ID: 16310588
[TBL] [Abstract][Full Text] [Related]
5. Late-onset Wilson's disease.
Ferenci P; Członkowska A; Merle U; Ferenc S; Gromadzka G; Yurdaydin C; Vogel W; Bruha R; Schmidt HT; Stremmel W
Gastroenterology; 2007 Apr; 132(4):1294-8. PubMed ID: 17433323
[TBL] [Abstract][Full Text] [Related]
6. 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; 70(5):457-62. PubMed ID: 23789284
[TBL] [Abstract][Full Text] [Related]
7. [Wilson disease - factors affecting clinical presentation].
Litwin T; Członkowska A
Neurol Neurochir Pol; 2013; 47(2):161-9. PubMed ID: 23650006
[TBL] [Abstract][Full Text] [Related]
8. High frequency of the c.3207C>A (p.H1069Q) mutation in ATP7B gene of Lithuanian patients with hepatic presentation of Wilson's disease.
Kucinskas L; Jeroch J; Vitkauskiene A; Sakalauskas R; Petrenkiene V; Kucinskas V; Naginiene R; Schmidt H; Kupcinskas L
World J Gastroenterol; 2008 Oct; 14(38):5876-9. PubMed ID: 18855987
[TBL] [Abstract][Full Text] [Related]
9. The His1069Gln mutation in the ATP7B gene in Romanian patients with Wilson's disease referred to a tertiary gastroenterology center.
Iacob R; Iacob S; Nastase A; Vagu C; Ene AM; Constantinescu A; Anghel D; Banica C; Paslaru L; Coriu D; Dima S; Gheorghe C; Ionica E; Gheorghe L
J Gastrointestin Liver Dis; 2012 Jun; 21(2):181-5. PubMed ID: 22720308
[TBL] [Abstract][Full Text] [Related]
10. Genotype phenotype correlation in Wilson's disease within families--a report on four south Indian families.
Santhosh S; Shaji RV; Eapen CE; Jayanthi V; Malathi S; Finny P; Thomas N; Chandy M; Kurian G; Chandy GM
World J Gastroenterol; 2008 Aug; 14(29):4672-6. PubMed ID: 18698682
[TBL] [Abstract][Full Text] [Related]
11. Genetic and Clinical Analysis in a Cohort of Patients with Wilson's Disease in Southwestern China.
Liu Y; Zhou H; Guo H; Bai Y
Arch Med Res; 2015 Feb; 46(2):164-9. PubMed ID: 25704634
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease.
Gromadzka G; Schmidt HH; Genschel J; Bochow B; Rodo M; Tarnacka B; Litwin T; Chabik G; Członkowska A
Clin Genet; 2005 Dec; 68(6):524-32. PubMed ID: 16283883
[TBL] [Abstract][Full Text] [Related]
14. Phenotype-genotype correlations in patients with Wilson's disease.
Ferenci P
Ann N Y Acad Sci; 2014 May; 1315():1-5. PubMed ID: 24517292
[TBL] [Abstract][Full Text] [Related]
15. Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patient.
Kok KF; Hoevenaars B; Waanders E; Drenth JP
Neth J Med; 2008 Sep; 66(8):348-50. PubMed ID: 18809983
[TBL] [Abstract][Full Text] [Related]
16. Genotype correlation with fine motor symptoms in patients with Wilson's disease.
Hermann W; Caca K; Eggers B; Villmann T; Clark D; Berr F; Wagner A
Eur Neurol; 2002; 48(2):97-101. PubMed ID: 12186999
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients.
Santhosh S; Shaji RV; Eapen CE; Jayanthi V; Malathi S; Chandy M; Stanley M; Selvi S; Kurian G; Chandy GM
Indian J Gastroenterol; 2006; 25(6):277-82. PubMed ID: 17264425
[TBL] [Abstract][Full Text] [Related]
19. Late onset fulminant Wilson's disease: a case report and review of the literature.
Weitzman E; Pappo O; Weiss P; Frydman M; Haviv-Yadid Y; Ben Ari Z
World J Gastroenterol; 2014 Dec; 20(46):17656-60. PubMed ID: 25516681
[TBL] [Abstract][Full Text] [Related]
20. From clinical and biochemical to molecular genetic diagnosis of Wilson disease in Latvia.
Krumina A; Keiss J; Sondore V; Chernushenko A; Cernevska G; Zarina A; Micule I; Piekuse L; Kreile M; Lace B; Krumina Z; Rozentale B
Genetika; 2008 Oct; 44(10):1379-84. PubMed ID: 19062534
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
