Results 41 to 50 of about 10,553 (137)

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

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

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

Comparative management practices of Wilson disease in Californian and Italian providers

open access: yesJournal of Health, Population and Nutrition
Background There is a scarcity of randomized and high-quality studies to aid clinicians in management and treatment of Wilson disease (WD). Even amongst society practice guidelines in North America and Europe, diagnosis and management of WD varies.
Sandy Vien   +4 more
doaj   +1 more source

A rare case of DIC in a patient with Wilson's disease: D-penicillamine. [PDF]

open access: yesHepatol Forum, 2022
Emre Parlar Y   +4 more
europepmc   +1 more source

Metabolic balances of sulfur in patients with hepatolenticular degeneration and effect of the use of D-penicillamine Balanços metabólicos do enxôfre em pacientes com degeneração hepatolenticular e efeito da administração de D-penicilamina

open access: yesArquivos 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
doaj  

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