Wilson disease (Q33250166)

24 July 2017

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title

[Wilson disease] (English)

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24 July 2017

Woimant F

1

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24 July 2017

Chaine P

2

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24 July 2017

Favrole P

3

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24 July 2017

Mikol J

4

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24 July 2017

Chappuis P

5

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24 July 2017

publication date

1 June 2006

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24 July 2017

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24 July 2017

volume

162

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24 July 2017

issue

6-7

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24 July 2017

page(s)

773-781

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Cerebral manifestation of Wilson's disease successfully treated with liver transplantation

24 July 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Elastosis perforans serpiginosa associated with pseudo-pseudoxanthoma elasticum during treatment of Wilson's disease with penicillamine.

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

1 reference

7 January 2021

Treatment of Wilson disease with ammonium tetrathiomolybdate. II. Initial therapy in 33 neurologically affected patients and follow-up with zinc therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Treatment of Wilson Disease With Ammonium Tetrathiomolybdate

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

The effects of B.A.L. in hepatolenticular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Improvement of cardiovascular autonomic dysfunction following anti-copper therapy in Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Clinical correlates of cerebral water diffusion in Wilson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Diagnosis and phenotypic classification of Wilson disease

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https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

1 reference

7 January 2021

Wilson disease in 1998: genetic, diagnostic and therapeutic aspects

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https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

The indication for liver transplant to improve neurological symptoms in a patient with Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Mid-brain pathology of Wilson's disease: MRI analysis of three cases

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Management of Wilson's disease with zinc sulphate. Experience in a series of 27 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Oral zinc in Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

A comparison of the mutation spectra of Menkes disease and Wilson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Hepatocellular carcinoma associated with Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Oculogyric crisis as an initial manifestation of Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Functional properties of the human copper-transporting ATPase ATP7B (the Wilson's disease protein) and regulation by metallochaperone Atox1

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Wilson's disease: MRI with clinical correlation

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Extensive cortico-subcortical lesions in Wilson's disease: clinico-pathological study of two cases

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Atypical MRI features of Wilson's disease: high signal in globus pallidus on T1-weighted images

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Haplotype and mutation analysis in Japanese patients with Wilson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Wilson's disease: diagnostic errors and clinical implications

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

A practice guideline on Wilson disease

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https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Initial and follow-up brain MRI findings and correlation with the clinical course in Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Cranial MR findings in Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Wilson disease: genetic basis of copper toxicity and natural history

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Albumin dialysis and Molecular Adsorbents Recirculating System (MARS) for acute Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Effect of liver transplantation on neurological manifestations in Wilson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Outcome of liver transplantation in Wilson's disease: A demonstrative case

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Wilson disease: findings at MR imaging and CT of the brain with clinical correlation

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Misdiagnosis revealed by genetic linkage analysis in a family with Wilson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Penicillamine, a new oral therapy for Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Treatment of Wilson's disease with trientine (triethylene tetramine) dihydrochloride

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Zinc-induced deterioration in Wilson's disease aborted by treatment with penicillamine, dimercaprol, and a novel zero copper diet

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Unusual digestive lesions in a patient with Wilson's disease treated with long-term penicillamine

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Structural basis for copper transfer by the metallochaperone for the Menkes/Wilson disease proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

PROGRESSIVE LENTICULAR DEGENERATION: A FAMILIAL NERVOUS DISEASE ASSOCIATED WITH CIRRHOSIS OF THE LIVER

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0035-3787%2806%2975080-9

7 January 2021

10.1016/S0035-3787(06)75080-9

Identifiers

DOI

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24 July 2017

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