(Q37743218)

22 August 2017

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title

Copper and liver disease. (English)

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22 August 2017

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D M Danks

1

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22 August 2017

publication date

1 January 1991

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European Journal of Pediatrics

22 August 2017

published in

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22 August 2017

volume

150

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22 August 2017

issue

3

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22 August 2017

page(s)

142-148

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https://scigraph.springernature.com/pub.10.1007/bf01963553

22 August 2017

exact match

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cites work

Worsening of neurologic syndrome in patients with Wilson's disease with initial penicillamine therapy

1 reference

https://api.crossref.org/works/10.1007%2FBF01963553

Regulation of aortic CuZn-superoxide dismutase with copper. Caeruloplasmin and albumin re-activate and transfer copper to the enzyme in culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01963553

Regulation of aortic CuZn-superoxide dismutase with copper. Effects in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01963553

Copper Storage Disease of the Liver and Chronic Dietary Copper Intoxication in Two Further German Infants Mimicking Indian Childhood Cirrhosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01963553

Idiopathic hepatic copper toxicosis in a child

21 January 2018

1 reference

12 December 2020

Prognosis of babies with neonatal hepatitis

1 reference

12 December 2020

Wilson's disease patients can be decoppered

1 reference

12 December 2020

Liver endothelium mediates the hepatocyte's uptake of ceruloplasmin

1 reference

12 December 2020

Wilson's disease: clinical presentation and use of prognostic index

1 reference

12 December 2020

Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease

1 reference

12 December 2020

Ascorbate enhances copper transport from ceruloplasmin into human K562 cells

1 reference

12 December 2020

Hereditary recurrent cholestasis with lymphoedema--two new families.

1 reference

12 December 2020

Can Wilson's disease patients be decoppered?

1 reference

12 December 2020

Studies of cholecystokinin-stimulated biliary secretions reveal a high molecular weight copper-binding substance in normal subjects that is absent in patients with Wilson's disease

1 reference

12 December 2020

Dangers of non-compliance in Wilson's disease

1 reference

12 December 2020

Wilson's disease in adults with cirrhosis but no neurological abnormalities

1 reference

12 December 2020

Copper-induced dystonia secondary to cholestatic liver disease

1 reference

12 December 2020

Penicillamine may detoxify copper in Wilson's disease

1 reference

12 December 2020

Reversible pancytopenia secondary to treatment with tetrathiomolybdate.

1 reference

12 December 2020

Cholestatic jaundice in infancy. The importance of familial and genetic factors in aetiology and prognosis

1 reference

12 December 2020

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

1 reference

12 December 2020

Secondary copper accumulation with neurological damage in child with chronic liver disease

1 reference

12 December 2020

Hepatic copper overload and features of Indian childhood cirrhosis in an American sibship

1 reference

12 December 2020

Copper transport from ceruloplasmin: characterization of the cellular uptake mechanism

1 reference

12 December 2020

The effects of ammonium tetrathiomolybdate intake on tissue copper and molybdenum in pregnant ewes and lambs

1 reference

12 December 2020

Morphologic and chemical studies on a murine mutation (toxic milk mice) resulting in hepatic copper toxicosis

1 reference

12 December 2020

Wilson's disease or chronic copper poisoning?

1 reference

12 December 2020

Indian childhood cirrhosis.

1 reference

12 December 2020

Intravenous administration of thiomolybdate for the prevention and treatment of chronic copper poisoning in sheep

1 reference

12 December 2020

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

1 reference

12 December 2020

Is Wilson's disease caused by a controller gene mutation resulting in perpetuation of the fetal mode of copper metabolism into childhood?

1 reference

12 December 2020

The effect of D-penicillamine on metallothionein mRNA levels and copper distribution in mouse hepatocytes

1 reference

12 December 2020

Penicillamine in Indian childhood cirrhosis

1 reference

12 December 2020

Studies of the aetiology of neonatal hepatitis and biliary atresia

1 reference

12 December 2020

Early introduction of copper-contaminated animal milk feeds as a possible cause of Indian childhood cirrhosis

1 reference

12 December 2020

Wilson's disease: an update, with emphasis on new approaches to treatment

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01963553

1 reference

22 August 2017

1 reference