Results 31 to 40 of about 1,630 (179)

Management of children and adolescents with Wilson Disease and neurological worsening following D–Penicillamine therapy: A single centre experience

open access: yesAnnals of Indian Academy of Neurology, 2022
Background: Most centers in developing countries prefer chelation therapy with D-penicillamine for the management of Wilson's disease (WD) because of its easy availability and affordability. Neurological worsening following treatment with D-penicillamine
Madhan Kumar   +5 more
doaj   +1 more source

Catatonia: A rare presentation of Wilson's disease

open access: yesIndustrial Psychiatry Journal, 2021
Wilson's disease (WD) or hepatolenticular degeneration is a rare inherited disorder of copper metabolism affecting both the liver and the central nervous system.
Supriya Davis   +4 more
doaj   +1 more source

A case of trientine overdose

open access: yesToxicology International, 2015
Wilson disease is a rare genetic hepatic and neurological disorder of copper accumulation. Trientine is usually used as a second line in the management of patients with this condition. We present a case of a large overdose of Trientine (60 g) resulting in self-limiting dizziness and vomiting with no further clinical sequelae or significant biochemical ...
Hashim, Ahmed, Parnell, Nick
openaire   +3 more sources

Developing an analytical method for quantification of trientine based on modified silver nanoparticles

open access: yesBMC Chemistry, 2023
Trientine or (N,N´-bis(2-aminoethyl)-1,2-ethanediamine (TETA) is a copper chelator and used in Wilson’s disease, is aliphatic amine that does not have UV absorbing groups.
Mahsa Khodadadi, Ali Shayanfar
doaj   +1 more source

Sensitive and Rapid determination of Trientine and N1-Acetyl Trientine in Human Plasma by LC-MS/MS for bioequivalence study [PDF]

open access: yes, 2019
A simple and robust method for simultaneous determination of Trientine and N1-Acetyl Trientine in human plasma by liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed and validated. The analyte and internal standard were extracted from
Parmar, Dharmesh   +4 more
core   +1 more source

Wilson’s disease [PDF]

open access: yesRomanian Journal of Neurology, 2011
A disturbance of copper metabolism causes hepatolenticular degeneration (Wilson’s disease), an autosomal recessive disorder whose genetic locus lies on the long arm of chromosome 13.
A. Hancu   +5 more
doaj   +1 more source

A Dose Escalation Study of Trientine Plus Carboplatin and Pegylated Liposomal Doxorubicin in Women With a First Relapse of Epithelial Ovarian, Tubal, and Peritoneal Cancer Within 12 Months After Platinum-Based Chemotherapy

open access: yesFrontiers in Oncology, 2019
Background: Epithelial ovarian cancer (EOC) is the leading cause of gynecological cancer-related deaths worldwide. Preclinical studies found that copper-lowering agents could re-sensitize platinum-resistant cancer cells by enhancing the human copper ...
Yu-Fang Huang   +5 more
doaj   +1 more source

Switching Pharmacological Treatment in Wilson Disease: Case Report and Recommendations

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2020
Background . Available treatments for Wilson disease (WD) prevent longterm complications of copper accumulation. Current anti-copper agents include zinc salts, penicillamine, and trientine.
Marcia Leung MD   +2 more
doaj   +1 more source

Targeting the Copper Transport System to Improve Treatment Efficacies of Platinum-Containing Drugs in Cancer Chemotherapy

open access: yesPharmaceuticals, 2021
The platinum (Pt)-containing antitumor drugs including cisplatin (cis-diamminedichloroplatinum II, cDDP), carboplatin, and oxaliplatin, have been the mainstay of cancer chemotherapy. These drugs are effective in treating many human malignancies.
Macus Tien Kuo   +3 more
doaj   +1 more source

Wilson disease in Northern Portugal: a long-term follow-up study

open access: yesOrphanet Journal of Rare Diseases, 2022
Introduction Wilson disease is an autosomal recessive disease of liver copper metabolism with predominant hepatic and neurological manifestations. Long-term data on the clinical follow-up and treatment efficacy are limited due to the low frequency of the
Isabel Garrido   +5 more
doaj   +1 more source

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