456 related articles for article (PubMed ID: 25516681)
41. 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]
42. Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).
Seidel J; Caca K; Schwab SG; Berr F; Wildenauer DB; Mentzel HJ; Horn N; Kauf E
Cell Mol Biol (Noisy-le-grand); 2001; 47 Online Pub():OL149-57. PubMed ID: 11936861
[TBL] [Abstract][Full Text] [Related]
43. Clinical and genetic analysis of pediatric patients with Wilson disease.
Şimşek Papur Ö; Aşık Akman S; Terzioğlu O
Turk J Gastroenterol; 2015 Sep; 26(5):397-403. PubMed ID: 26215059
[TBL] [Abstract][Full Text] [Related]
44. Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
de Bie P; van de Sluis B; Burstein E; van de Berghe PV; Muller P; Berger R; Gitlin JD; Wijmenga C; Klomp LW
Gastroenterology; 2007 Oct; 133(4):1316-26. PubMed ID: 17919502
[TBL] [Abstract][Full Text] [Related]
45. A novel ATP7B gene mutation in a liver failure patient with normal ceruloplasmin and low serum alkaline phosphatase.
Chen L; Li X; Zheng Z; Lu X; Lin M; Pan C; Liu J
Gene; 2014 Mar; 538(1):204-6. PubMed ID: 24476933
[TBL] [Abstract][Full Text] [Related]
46. Neurological manifestations and ATP7B mutations in Wilson's disease.
Machado AA; Deguti MM; Genschel J; Cançado EL; Bochow B; Schmidt H; Barbosa ER
Parkinsonism Relat Disord; 2008; 14(3):246-9. PubMed ID: 17897870
[TBL] [Abstract][Full Text] [Related]
47. Gene mutations in Wilson disease in Egyptian children: report on two novel mutations.
El-Mougy FA; Sharaf SA; Elsharkawy MM; Mandour IA; El-Essawy RA; Eldin AM; Helmy HM; Soliman DH; Selim LH; Sharafeldin HM; Mogahed EA; El-Karaksy HM
Arab J Gastroenterol; 2014; 15(3-4):114-8. PubMed ID: 25465132
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. Wilson's disease: a comprehensive review of the molecular mechanisms.
Wu F; Wang J; Pu C; Qiao L; Jiang C
Int J Mol Sci; 2015 Mar; 16(3):6419-31. PubMed ID: 25803104
[TBL] [Abstract][Full Text] [Related]
50. Hepatocyte transplantation in the Long Evans Cinnamon rat model of Wilson's disease.
Park SM; Vo K; Lallier M; Cloutier AS; Brochu P; Alvarez F; Martin SR
Cell Transplant; 2006; 15(1):13-22. PubMed ID: 16700326
[TBL] [Abstract][Full Text] [Related]
51. 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]
52. Systems biology approach to Wilson's disease.
Burkhead JL; Gray LW; Lutsenko S
Biometals; 2011 Jun; 24(3):455-66. PubMed ID: 21380607
[TBL] [Abstract][Full Text] [Related]
53. Spectrum and Classification of ATP7B Variants in a Large Cohort of Chinese Patients with Wilson's Disease Guides Genetic Diagnosis.
Dong Y; Ni W; Chen WJ; Wan B; Zhao GX; Shi ZQ; Zhang Y; Wang N; Yu L; Xu JF; Wu ZY
Theranostics; 2016; 6(5):638-49. PubMed ID: 27022412
[TBL] [Abstract][Full Text] [Related]
54. Kayser-Fleischer ring.
Suvarna JC
J Postgrad Med; 2008; 54(3):238-40. PubMed ID: 18626182
[TBL] [Abstract][Full Text] [Related]
55. ATP7B Gene Mutations in Croatian Patients with Wilson Disease.
Ljubić H; Kalauz M; Telarović S; Ferenci P; Ostojić R; Noli MC; Lepori MB; Hrstić I; Vuković J; Premužić M; Radić D; Ravić KG; Sertić J; Merkler A; Barišić AA; Loudianos G; Vucelić B
Genet Test Mol Biomarkers; 2016 Mar; 20(3):112-7. PubMed ID: 26799313
[TBL] [Abstract][Full Text] [Related]
56. Genetics of Wilson's disease: a clinical perspective.
Kumar SS; Kurian G; Eapen CE; Roberts EA
Indian J Gastroenterol; 2012 Dec; 31(6):285-93. PubMed ID: 22941676
[TBL] [Abstract][Full Text] [Related]
57. Wilson's Disease.
Pfeiffer RF
Semin Neurol; 2007 Apr; 27(2):123-32. PubMed ID: 17390257
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Wilson's disease: an update.
Das SK; Ray K
Nat Clin Pract Neurol; 2006 Sep; 2(9):482-93. PubMed ID: 16932613
[TBL] [Abstract][Full Text] [Related]
60. 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; 56(5):302-4. PubMed ID: 14514926
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
