about
Penicinillamine for Wilson's diseaseWilson's disease with severe hepatic insufficiency: beneficial effects of early administration of D-penicillamineGenotype-phenotype correlations in a mountain population community with high prevalence of Wilson's disease: genetic and clinical homogeneityPhenotypic and genetic characterization of a cohort of pediatric Wilson disease patients.Bipolar disorders and Wilson's disease.Wilson's disease in Scotland.Clinical presentation and mutations in Danish patients with Wilson disease.Diagnosis of Wilson's disease: an experience over three decadesImmunohistochemical features of the portal tract mononuclear cell infiltrate in chronic aggressive hepatitisWilson's disease: an analysis of 28 Brazilian children.Wilson's disease: clinical, genetic and pharmacological findings.Quality of Life and Psychiatric Symptoms in Wilson's Disease: the Relevance of Bipolar DisordersPresentation, diagnosis and outcome of predominantly hepatic Wilson's disease in adult Saudi patients: a single centre experience.Prospective evaluation of the diagnostic accuracy of hepatic copper content, as determined using the entire core of a liver biopsy sample.Mutational analysis of ATP7B in Chinese Wilson disease patientsGeographic distribution of ATP7B mutations in Wilson disease.Evaluation of Kayser-Fleischer ring in Wilson disease by anterior segment optical coherence tomography.Metallothionein in physiological and physiopathological processes.A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient.Expression of the Wilson disease gene is deficient in the Long-Evans Cinnamon rat.Genes of the copper pathway.Recurrent limb weakness in a 17-year-old boy.Isolated persistent elevation of alanine transaminase for early diagnosis of pre-symptomatic Wilson's disease in Chinese children.Usefulness of penicillamine-stimulated urinary copper excretion in the diagnosis of adult Wilson's disease.Relative exchangeable copper: A valuable tool for the diagnosis of Wilson disease.Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B.Compliant treatment with anti-copper agents prevents clinically overt Wilson's disease in pre-symptomatic patients.[Diagnostics of Wilson's disease].Copper toxicosis in the Bedlington terrier: a diagnostic dilemma.Potential of the international scoring system for the diagnosis of Wilson disease to differentiate Japanese patients who need anti-copper treatment.Copper-associated liver disease in North Ronaldsay sheep: a possible animal model for non-Wilsonian hepatic copper toxicosis of infancy and childhood
P2860
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P2860
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年学术文章
@wuu
1990年学术文章
@zh-cn
1990年学术文章
@zh-hans
1990年学术文章
@zh-my
1990年学术文章
@zh-sg
1990年學術文章
@yue
1990年學術文章
@zh
1990年學術文章
@zh-hant
name
Perspectives on Wilson's disease.
@en
Perspectives on Wilson's disease.
@nl
type
label
Perspectives on Wilson's disease.
@en
Perspectives on Wilson's disease.
@nl
prefLabel
Perspectives on Wilson's disease.
@en
Perspectives on Wilson's disease.
@nl
P356
P1433
P1476
Perspectives on Wilson's disease.
@en
P2093
Sternlieb I
P2860
P304
P356
10.1002/HEP.1840120526
P407
P577
1990-11-01T00:00:00Z