(Q42850401)

8 November 2017

title

Re-evaluation of the diagnostic criteria for Wilson disease in children with mild liver disease (English)

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8 November 2017

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Emanuele Nicastro

1

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Raffaele Iorio

object named as

Raffaele Iorio

5

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Pietro Vajro

object named as

Pietro Vajro

3

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author name string

Giusy Ranucci

2

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8 November 2017

Angela Vegnente

4

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8 November 2017

language of work or name

English

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publication date

21 October 2010

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8 November 2017

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8 November 2017

volume

52

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8 November 2017

issue

6

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8 November 2017

page(s)

1948-1956

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8 November 2017

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7 January 2021

Diagnosis and treatment of Wilson disease: an update

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Wilson's disease in children: 37-year experience and revised King's score for liver transplantation

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Serum transaminases in children with Wilson's disease

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A high index of suspicion: the key to an early diagnosis of Wilson's disease in childhood

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Neurological manifestations in Wilson's disease: Report of 119 cases.

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7 January 2021

Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study

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7 January 2021

Long-term outcome in Serbian patients with Wilson disease

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Re-evaluation of the penicillamine challenge test in the diagnosis of Wilson’s disease in children

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7 January 2021

Wilson disease: diagnostic dilemmas?

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7 January 2021

Diagnosis and phenotypic classification of Wilson disease

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7 January 2021

Value of urinary copper excretion after penicillamine challenge in the diagnosis of Wilson's disease

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7 January 2021

Microwave energy for acid decomposition at elevated temperatures and pressures using biological and botanical samples

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7 January 2021

Chronic hepatitis. An update on terminology and reporting.

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Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin

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Diagnostic accuracy of serum ceruloplasmin in Wilson disease: determination of sensitivity and specificity by ROC curve analysis among ATP7B-genotyped subjects

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7 January 2021

Diagnostic value of quantitative hepatic copper determination in patients with Wilson's Disease

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7 January 2021

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7 January 2021

Cryptogenic liver disease in four children: a novel congenital disorder of glycosylation

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7 January 2021

Genotype-phenotype correlation in Italian children with Wilson's disease

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7 January 2021

Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease.

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7 January 2021

Diagnosis of Wilson's disease: an experience over three decades

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7 January 2021

Wilson's disease in patients presenting with liver disease: a diagnostic challenge.

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7 January 2021

Wilson disease in children: analysis of 57 cases

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7 January 2021

Copper transport and metabolism are normal in aceruloplasminemic mice

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7 January 2021

Association of copper to metallothionein in hepatic lysosomes of Long-Evans cinnamon (LEC) rats during the development of hepatitis [se e comments]

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7 January 2021

Chronological changes in tissue copper, zinc and iron in the toxic milk mouse and effects of copper loading.

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7 January 2021

Mitochondrial structure and function in the untreated Jackson toxic milk (tx-j) mouse, a model for Wilson disease

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7 January 2021

Identifiers

DOI

10.1002/HEP.23910

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release_birkx7sjszfhzjrd2izfkp2odm

8 November 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/birkx7sjszfhzjrd2izfkp2odm

24 November 2022

mapped directly with Wikidata item

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