Results 61 to 70 of about 12,790 (151)

D-Penicillamine-Induced Stevens–Johnson Syndrome in a Patient with Gold Cyanide Intoxication: A Case Report

open access: yesClinical, Cosmetic and Investigational Dermatology
Tanaporn Anuntrangsee, Kumutnart Chanprapaph, Wimolsiri Iamsumang Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, ThailandCorrespondence: Wimolsiri Iamsumang, Division of Dermatology,
Anuntrangsee T   +2 more
doaj  

Crystal structure of S,N-dibenzyl-d-penicillamine monohydrate

open access: yesActa Crystallographica Section E, 2014
In the asymmetric unit of the title compound, C19H23NO2S·H2O, there are two independent organic molecules and two water molecules. Both organic molecules exist as the zwitterionic form.
Nobuto Yoshinari, Takumi Konno
doaj   +1 more source

Comparative analysis of clinical outcomes and safety profile of trientine and d-penicillamine in the management of Wilson’s disease: A systematic review and meta-analysis

open access: yesRare
Introduction: Wilson disease (WD) is a rare metabolic disorder of copper metabolism, requiring life-long therapy, usually with D-penicillamine or trientine. This review compares their clinical effectiveness and safety.
Hafiz Muhammad Ehsan Arshad   +5 more
doaj   +1 more source

The effect of surface charge on nonspecific uptake and cytotoxicity of CdSe/ZnS core/shell quantum dots

open access: yesBeilstein Journal of Nanotechnology, 2015
In this work, cytotoxicity and cellular impedance response was compared for CdSe/ZnS core/shell quantum dots (QDs) with positively charged cysteamine–QDs, negatively charged dihydrolipoic acid–QDs and zwitterionic D-penicillamine–QDs exposed to canine ...
Vladimir V. Breus   +4 more
doaj   +1 more source

WILSON'S DISEASE IN CHILDREN, REPORT OF 25 CASES [PDF]

open access: yesActa Medica Iranica, 1984
We conducted a retrospective study of 25 cases (15 boys and 12 girls) of Wilson's disease(Hepatolenticular degeneration)spanning a period of 8 years. Age at the time of diagnosis ranged between 3-17 years. The f ollowing clinical forms were observed:
Y. AGHIGHI, R. AFTENDELIANS
doaj  

Nephrotic syndrome after treatment with d-penicillamine in a pediatric patient with Wilson’s disease

open access: yesLa Pediatria Medica e Chirurgica, 2012
We describe a case of nephrotic syndrome (NS) after a 7 months treatment with D-penicillamine in a 14 years old girl with Wilson’s disease , with a prompt regression at the discontinuation of the drug.
M. Farallo   +4 more
doaj   +1 more source

Evolução para remissão clínica completa em esclerose sistêmica Progression into clinical remission in systemic sclerosis

open access: yesRevista Brasileira de Reumatologia, 2004
OBJETIVO: mostrar a evolução de quatro pacientes para remissão clínica completa da esclerose sistêmica (ES), sem necessidade de tratamento medicamentoso atual, após uso de D-penicilamina como medicação principal.
Leandro Antônio Cichoski   +3 more
doaj   +1 more source

Non-ceruloplasmin copper and urinary copper in clinically stable Wilson disease: Alignment with recommended targets

open access: yesJHEP Reports
Background & Aims: Wilson disease (WD) is caused by accumulation of copper primarily in the liver and brain. During maintenance therapy of WD with D-penicillamine, current guidelines recommend on-treatment ranges of urinary copper excretion (UCE) of ...
Peter Ott   +16 more
doaj   +1 more source

Evaluation of vitamin B6 supplementation in Wilson's disease patients treated with D-penicillamine. [PDF]

open access: yesBMJ Open Gastroenterol, 2023
Mbala J   +4 more
europepmc   +1 more source

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