Results 21 to 30 of about 10,553 (137)
Development of copper electrochemical sensor using D-penicillamine functionalized graphene oxide modified electrode [PDF]
شیمی کاربردی روز, 2023 In this research, graphene oxide (GO) was functionalized with D-penicillamine (DPA) and used to develop an electrochemical sensor for Cu(II) cation. For the successful synthesis of D-penicillamine-functionalized graphene oxide (DPA-GO), Fourier Transfer ...
Maryam Khordadpour Siahkal Mahalleh +2 more
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Synthesis and Characterization of Gold Chiral Nanoparticles Functionalized by a Chiral Drug
Nanomaterials, 2023 Inorganic chiral nanoparticles are attracting more and more attention due to their peculiar optical properties and potential biological applications, such as bioimaging, therapeutics, and diagnostics.
Simona Bettini +8 more
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Nephrotic syndrome after treatment with D-penicillamine in a patient with Wilson’s disease
Romanian Journal of Laboratory Medicine, 2014 Wilson’s disease is an inherited autosomal recessive disorder of copper balance leading to accumulation of copper mainly in liver and brain result from absent or reduced function of copper-transporting P-type ATPase.
Kostadinova Anna D. +3 more
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Arquivos de Neuro-Psiquiatria, 1969 The metabolic balances of sulfur in two cases of hepatolenticular degeneration were studied. A positive balance was found in both cases; in one patient submitted to mixed diet, the average was significantly higher than the normal mean. The administration
Horacio M. Canelas +2 more
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Validity of D-penicillamine in experimental cerebral vasospasm therapy
Interdisciplinary NeurosurgeryBackground: Cerebral vasospasm is a reversible vessel constriction following subarachnoid hemorrhage. Immunoreactive and inflammatory mechanisms induce long-term vasoconstriction and vessel dilatation inhibition.
Ersin Haciyakupoglu +6 more
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Manic episode induced by discontinuance of D-penicillamine treatment in Wilson’s disease
Psychiatry and Clinical Psychopharmacology, 2021 Wilson’s disease (WD) is a rarely seen autosomal recessive inherited genetic disease of copper metabolism, which leads to various hepatic, orbital and neuropsychiatric disorders.
Ayse Nur Inci Kenar, Husnu Menteseoglu
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Response to different therapeutic approaches in Wilson disease. A long-term follow up study
Annals of Hepatology, 2012 Background and aims. There are certain areas of uncertainty regarding the best therapeutic approach in patients diagnosed with Wilson Disease (WD). Our aim was to assess treatment response to different therapies in a cohort of WD patients followed in a ...
Beatriz Rodríguez +2 more
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Wilson's disease update: An Indian perspective
Annals of Indian Academy of Neurology, 2022 Wilson's disease (WD) is an autosomal recessive disorder due to ATP7B gene mutation, resulting in defective copper metabolism, with liver and brain being primarily affected.
Kalyan Bhattacharya, Bindu Thankappan
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مجله دانشگاه علوم پزشکی گرگان, 2016 Background and Objective: Wilson’s disease (WD) is caused by mutation to the cooer-transporting gene ATP7B. Chelation therapy is the main protochol of treatment for patients with Wilson’s disease.
Fani N +4 more
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Autopsy and Case Reports, 2021 Long term use of D-penicillamine for Wilson’s disease can be associated with many adverse reactions and systemic side effects. We report the case of a 28-year-old male patient diagnosed with Wilson’s disease presenting with a serpiginous raised ...
Swagatika Samal, Mukund Sable
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