Diagnosis of Wilson's disease: an experience over three decades
about
Late onset fulminant Wilson's disease: a case report and review of the literaturePhenotype-genotype correlation in Wilson disease in a large Lebanese family: association of c.2299insC with hepatic and of p. Ala1003Thr with neurologic phenotypeLiver cirrhosis in patients newly diagnosed with neurological phenotype of Wilson's disease.Wilson disease: Canadian perspectives on presentation and outcomes from an adult ambulatory setting.[Wilson's disease: about a family case].1H NMR-based metabolomics investigation of copper-laden rat: a model of Wilson's disease.Dietary copper triggers onset of fulminant hepatitis in the Long-Evans cinnamon rat model.Prospective evaluation of the diagnostic accuracy of hepatic copper content, as determined using the entire core of a liver biopsy sample.Long-term effects of a combination of D-penicillamine and zinc salts in the treatment of Wilson's disease in children.Screening for Wilson disease in acute liver failure: a comparison of currently available diagnostic tests.Diagnosis of Wilson disease in young children: molecular genetic testing and a paradigm shift from the laboratory diagnosis.Galactorrhea with menstrual irregularity: something other than a prolactinoma?Nutritional influences in selected gastrointestinal diseases.Wilson's disease masquerading as nonalcoholic steatohepatitis.Identification of novel mutations and the three most common mutations in the human ATP7B gene of Korean patients with Wilson disease.Rapid detection of mutations in Wilson disease gene ATP7B by DNA strip technology.Uneven distribution of hepatic copper concentration and diagnostic value of double-sample biopsy in Wilson's disease.Usefulness of penicillamine-stimulated urinary copper excretion in the diagnosis of adult Wilson's disease.Reversion of gold nanoparticle aggregates for the detection of Cu2+ and its application in immunoassays.Relative exchangeable copper: A valuable tool for the diagnosis of Wilson disease.The optimal threshold of serum ceruloplasmin in the diagnosis of Wilson's disease: A large hospital-based study.Reduced serum caeruloplasmin levels in non-wilsonian movement disorders.Comprehensive analysis on clinical features of Wilson's disease: an experience over 28 years with 133 cases.Cure of ventriculitis and central nervous system shunt infection by Staphylococcus epidermidis with vancomycin by intraventricular injection in a liver transplant recipient.Wilson disease: a most unusual patient.
P2860
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P2860
Diagnosis of Wilson's disease: an experience over three decades
description
2000 nî lūn-bûn
@nan
2000 թուականի Մարտին հրատարակուած գիտական յօդուած
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2000 թվականի մարտին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
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name
Diagnosis of Wilson's disease: an experience over three decades
@ast
Diagnosis of Wilson's disease: an experience over three decades
@en
type
label
Diagnosis of Wilson's disease: an experience over three decades
@ast
Diagnosis of Wilson's disease: an experience over three decades
@en
prefLabel
Diagnosis of Wilson's disease: an experience over three decades
@ast
Diagnosis of Wilson's disease: an experience over three decades
@en
P2093
P2860
P356
P1433
P1476
Diagnosis of Wilson's disease: an experience over three decades
@en
P2093
P2860
P304
P356
10.1136/GUT.46.3.415
P407
P577
2000-03-01T00:00:00Z