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Wilson Disease: Copper-Mediated Cuproptosis, Iron-Related Ferroptosis, and Clinical Highlights, with Comprehensive and Critical Analysis Update.
Teschke R, Eickhoff A. Teschke R, et al. Int J Mol Sci. 2024 Apr 26;25(9):4753. doi: 10.3390/ijms25094753. Int J Mol Sci. 2024. PMID: 38731973 Free PMC article. Review.
Wilson disease is a genetic disorder of the liver characterized by excess accumulation of copper, which is found ubiquitously on earth and normally enters the human body in small amounts via the food chain. ...In addition, Coombs-negative hemolytic anemia is a key f …
Wilson disease is a genetic disorder of the liver characterized by excess accumulation of copper, which is found ubiquitously …
Effects of tetrathiomolybdate on copper metabolism in healthy volunteers and in patients with Wilson disease.
Kirk FT, Munk DE, Swenson ES, Quicquaro AM, Vendelbo MH, Larsen A, Schilsky ML, Ott P, Sandahl TD. Kirk FT, et al. J Hepatol. 2024 Apr;80(4):586-595. doi: 10.1016/j.jhep.2023.11.023. Epub 2023 Dec 10. J Hepatol. 2024. PMID: 38081365 Free article. Clinical Trial.
BACKGROUND & AIMS: In Wilson disease (WD), copper accumulates in the liver and brain causing disease. Bis-choline tetrathiomolybdate (TTM) is a potent copper chelator that may be associated with a lower risk of inducing paradoxical neurological worsening than co …
BACKGROUND & AIMS: In Wilson disease (WD), copper accumulates in the liver and brain causing disease. Bis-choline tetrathi …
Deadly excess copper.
Sailer J, Nagel J, Akdogan B, Jauch AT, Engler J, Knolle PA, Zischka H. Sailer J, et al. Redox Biol. 2024 Sep;75:103256. doi: 10.1016/j.redox.2024.103256. Epub 2024 Jun 28. Redox Biol. 2024. PMID: 38959622 Free PMC article. Review.
Consequently, malfunction of copper enzymes/transporters, as is the case in hereditary Wilson disease that affects the intracellular copper transporter ATP7B, comes with serious cellular damage. ...
Consequently, malfunction of copper enzymes/transporters, as is the case in hereditary Wilson disease that affects the intrace …
Wilson Disease: Novel Diagnostic and Therapeutic Approaches.
Mariño Z, Schilsky ML. Mariño Z, et al. Semin Liver Dis. 2025 Jun;45(2):221-235. doi: 10.1055/a-2460-8999. Epub 2024 Nov 4. Semin Liver Dis. 2025. PMID: 39496313 Free article. Review.
The Wilson disease (WD) research field is rapidly evolving, and new diagnostic and therapeutical approaches are expected to be change-gamers in the disease for the incoming years, after decades of slow changing options. ...
The Wilson disease (WD) research field is rapidly evolving, and new diagnostic and therapeutical approaches are expected to be …
Pitfalls in the Diagnosis of Wilson Disease.
Roy D, Mukherjee A, Chakravarty A. Roy D, et al. Curr Neurol Neurosci Rep. 2025 Jun 12;25(1):40. doi: 10.1007/s11910-025-01424-8. Curr Neurol Neurosci Rep. 2025. PMID: 40504409 Review.
PURPOSE OF REVIEW: Wilson disease (WD), an uncommon autosomal recessive (AR) hereditary disorder characterized by abnormal accumulation of copper primarily in the liver and secondarily in other organs like the brain, is caused by a deficiency in the ATP7B transporte …
PURPOSE OF REVIEW: Wilson disease (WD), an uncommon autosomal recessive (AR) hereditary disorder characterized by abnormal acc …
Liver transplantation for Wilson disease: Current knowledge and future perspectives.
Ferrarese A, Cazzagon N, Burra P. Ferrarese A, et al. Liver Transpl. 2024 Dec 1;30(12):1289-1303. doi: 10.1097/LVT.0000000000000422. Epub 2024 Jun 19. Liver Transpl. 2024. PMID: 38899966 Review.
Liver transplantation currently represents a therapeutic option for patients with Wilson disease presenting with end-stage liver disease or acute liver failure. Indeed, it has been associated with excellent postoperative survival curves in view of young age at trans …
Liver transplantation currently represents a therapeutic option for patients with Wilson disease presenting with end-stage liv …
Prion protein promotes copper toxicity in Wilson disease.
Petruzzelli R, Catalano F, Crispino R, Polishchuk EV, Elia M, Masone A, Lavigna G, Grasso A, Battipaglia M, Sepe LV, Akdogan B, Reinold Q, Del Prete E, Carrella D, Torella A, Nigro V, Caruso E, Innocenti N, Biasini E, Puchkova LV, Indrieri A, Ilyechova EY, Piccolo P, Zischka H, Chiesa R, Polishchuk RS. Petruzzelli R, et al. Nat Commun. 2025 Feb 8;16(1):1468. doi: 10.1038/s41467-025-56740-x. Nat Commun. 2025. PMID: 39922819 Free PMC article.
Dysfunction in key components of this network leads to the disruption of Cu homeostasis, resulting in fatal disorders such as Wilson disease, which is caused by mutations in the hepatic Cu efflux transporter ATP7B. ...Suppression of PrP significantly reduces Cu toxi …
Dysfunction in key components of this network leads to the disruption of Cu homeostasis, resulting in fatal disorders such as Wilson …
Amantadine-induced psychosis in Wilson disease.
Suhas S, Singh GK, Sreeraj VS, Venkatasubramanian G. Suhas S, et al. Natl Med J India. 2024 May-Jun;37(3):141-142. doi: 10.25259/NMJI_643_21. Natl Med J India. 2024. PMID: 39399997
Wilson disease is a rare genetic disorder of copper metabolism causing hepatic dysfunction and neuro-psychiatric manifestations. While psychosis in Wilson disease is uncommon, it can occur, especially with certain medications. We describe a 40-year-old …
Wilson disease is a rare genetic disorder of copper metabolism causing hepatic dysfunction and neuro-psychiatric manifestation …
Nano-Mediated Molecular Targeting in Diagnosis and Mitigation of Wilson Disease.
Chaturvedi A, Sharma S, Shukla R. Chaturvedi A, et al. Mol Neurobiol. 2024 Jul;61(7):4240-4258. doi: 10.1007/s12035-023-03816-8. Epub 2023 Dec 8. Mol Neurobiol. 2024. PMID: 38066399 Review.
Wilson disease, a rare genetic disorder resulting from mutations in the ATP7B gene disrupts copper metabolism, leading to its harmful accumulation in hepatocytes, the brain, and other organs. ...Nanotechnology-driven formulations are showing promise for both treatme …
Wilson disease, a rare genetic disorder resulting from mutations in the ATP7B gene disrupts copper metabolism, leading to its …
Copper impairs the intestinal barrier integrity in Wilson disease.
Fontes A, Pierson H, Bierła JB, Eberhagen C, Kinschel J, Akdogan B, Rieder T, Sailer J, Reinold Q, Cielecka-Kuszyk J, Szymańska S, Neff F, Steiger K, Seelbach O, Zibert A, Schmidt HH, Hauck SM, von Toerne C, Michalke B, Semrau JD, DiSpirito AM, Ramalho-Santos J, Kroemer G, Polishchuk R, Azul AM, DiSpirito A, Socha P, Lutsenko S, Zischka H. Fontes A, et al. Metabolism. 2024 Sep;158:155973. doi: 10.1016/j.metabol.2024.155973. Epub 2024 Jul 8. Metabolism. 2024. PMID: 38986805 Free article.
In Wilson disease (WD), liver copper (Cu) excess, caused by mutations in the ATPase Cu transporting beta (ATP7B), has been extensively studied. ...
In Wilson disease (WD), liver copper (Cu) excess, caused by mutations in the ATPase Cu transporting beta (ATP7B), has been ext …
105 results