324 related articles for article (PubMed ID: 34341141)
41. Toxic milk mice models of Wilson's disease.
Hadrian K; Przybyłkowski A
Mol Biol Rep; 2021 Feb; 48(2):1903-1914. PubMed ID: 33590415
[TBL] [Abstract][Full Text] [Related]
42. Wilson's disease: Fatal when overlooked, curable when diagnosed.
Ferenci P; Ott P
J Hepatol; 2019 Jul; 71(1):222-224. PubMed ID: 31126728
[No Abstract] [Full Text] [Related]
43. Copper-Induced Epigenetic Changes Shape the Clinical Phenotype in Wilson's Disease.
Fanni D; Gerosa C; Nurchi VM; Cappai R; Mureddu M; Eyken PV; Saba L; Manchia M; Faa G
Curr Med Chem; 2021; 28(14):2707-2716. PubMed ID: 32744959
[TBL] [Abstract][Full Text] [Related]
44. Wilson's disease: A new perspective review on its genetics, diagnosis and treatment.
Saba L; Tiwari A; Biswas M; Gupta SK; Godia-Cuadrado E; Chaturvedi A; Turk M; Suri HS; Orru S; Sanches JM; Carcassi C; Marinho RT; Asare CK; Khanna NN; B K M; Suri JS
Front Biosci (Elite Ed); 2019 Jun; 11(1):166-185. PubMed ID: 31136971
[TBL] [Abstract][Full Text] [Related]
45. Metallothionein is elevated in liver and duodenum of Atp7b
Zhang CC; Volkmann M; Tuma S; Stremmel W; Merle U
Biometals; 2018 Aug; 31(4):617-625. PubMed ID: 29732486
[TBL] [Abstract][Full Text] [Related]
46. Currently Clinical Views on Genetics of Wilson's Disease.
Chen C; Shen B; Xiao JJ; Wu R; Duff Canning SJ; Wang XP
Chin Med J (Engl); 2015 Jul; 128(13):1826-30. PubMed ID: 26112727
[TBL] [Abstract][Full Text] [Related]
47. Role for Biochemical Assays and Kayser-Fleischer Rings in Diagnosis of Wilson's Disease.
Dong Y; Wang RM; Yang GM; Yu H; Xu WQ; Xie JJ; Zhang Y; Chen YC; Ni W; Wu ZY
Clin Gastroenterol Hepatol; 2021 Mar; 19(3):590-596. PubMed ID: 32485301
[TBL] [Abstract][Full Text] [Related]
48. 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; 19(1):61. PubMed ID: 29649982
[TBL] [Abstract][Full Text] [Related]
49. High genetic carrier frequency of Wilson's disease in France: discrepancies with clinical prevalence.
Collet C; Laplanche JL; Page J; Morel H; Woimant F; Poujois A
BMC Med Genet; 2018 Aug; 19(1):143. PubMed ID: 30097039
[TBL] [Abstract][Full Text] [Related]
50. Functional characterization of novel or yet uncharacterized ATP7B missense variants detected in patients with clinical Wilson's disease.
Stalke A; Behrendt A; Hennig F; Gohlke H; Buhl N; Reinkens T; Baumann U; Schlegelberger B; Illig T; Pfister ED; Skawran B
Clin Genet; 2023 Aug; 104(2):174-185. PubMed ID: 37157876
[TBL] [Abstract][Full Text] [Related]
51. Wilson's disease, 100 years later….
Trocello JM; Broussolle E; Girardot-Tinant N; Pelosse M; Lachaux A; Lloyd C; Woimant F
Rev Neurol (Paris); 2013 Dec; 169(12):936-43. PubMed ID: 24119853
[TBL] [Abstract][Full Text] [Related]
52. In
Sharma Y; Liu J; Kristian KE; Follenzi A; Gupta S
Gene Expr; 2018 Dec; 19(1):15-24. PubMed ID: 30029699
[TBL] [Abstract][Full Text] [Related]
53. Rare co-occurrence of multiple sclerosis and Wilson's disease - case report.
Despotov K; Klivényi P; Nagy I; Pálvölgyi A; Vécsei L; Rajda C
BMC Neurol; 2022 May; 22(1):178. PubMed ID: 35578211
[TBL] [Abstract][Full Text] [Related]
54. Atypical case of Wilson's disease with psychotic onset, low 24 hour urine copper and the absence of Kayser-Fleischer rings.
Krstić D; Antonijević J; Špirić Ž
Vojnosanit Pregl; 2014 Dec; 71(12):1155-8. PubMed ID: 25639007
[TBL] [Abstract][Full Text] [Related]
55. Extrapyramidal symptoms in Wilson's disease are associated with olfactory dysfunction.
Mueller A; Reuner U; Landis B; Kitzler H; Reichmann H; Hummel T
Mov Disord; 2006 Sep; 21(9):1311-6. PubMed ID: 16763975
[TBL] [Abstract][Full Text] [Related]
56. Neurological Deterioration in Wilson's Disease-Types, Etiology, Course, and Management.
Litwin T; Antos A; Bembenek J; Cz Onkowska A
Discov Med; 2024 Apr; 36(183):646-654. PubMed ID: 38665014
[TBL] [Abstract][Full Text] [Related]
57. 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]
58. A Special Case of Cirrhosis with a Novel ATP7B Mutation and Occult Chronic HBV Infection.
Jiang Y; Chen M; Ruan Y; Ma J; Li N
J Coll Physicians Surg Pak; 2021 Oct; 31(10):1231-1233. PubMed ID: 34601848
[TBL] [Abstract][Full Text] [Related]
59. Characteristics of neurological Wilson's disease without Kayser-Fleischer ring.
Youn J; Kim JS; Kim HT; Lee JY; Lee PH; Ki CS; Cho JW
J Neurol Sci; 2012 Dec; 323(1-2):183-6. PubMed ID: 23043908
[TBL] [Abstract][Full Text] [Related]
60. Generation of ZJUi003-A, an induced pluripotent stem cell line from a Wilson's disease patient carrying a c.180_181del mutation in ATP7B gene.
Wang J; Su J; Gong T; Li T; Shen J; Wang H; Xie H; Zhou L; Zheng S; Liang P
Stem Cell Res; 2020 Jul; 46():101873. PubMed ID: 32534167
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
