DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE. - Wikidata - awgldk - TriplyDB

DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

http://www.wikidata.org/entity/Q34010551

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ABSORPTION OF COPPER IN MALABSORPTION SYNDROMES.THE INCORPORATION OF COPPER INTO CERULOPLASMIN IN VIVO: STUDIES WITH COPPER AND COPPER Ceruloplasmin in Wilson's disease A genetic study of Wilson's disease: evidence for heterogeneity.Reduced oxidase activity in the caeruloplasmin of two families with Wilson's disease Copper deficiency myelopathy.Studies on the oxidase properties of ceruloplasmin: factors in normal and Wilson's-disease serum affecting oxidase activity.Caeruloplasmin: physiological and pathological perspectives.Orthotopic liver transplantation for Wilson's disease Oral zinc sulphate for Wilson's disease.An assessment of efficiency in potential screening for Wilson's disease.

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P2860

DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

http://www.wikidata.org/entity/Q34010551

description

1961 nî lūn-bûn

@nan

1961 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

1961 թվականի ապրիլին հրատարակված գիտական հոդված

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1961年の論文

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1961年論文

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1961年論文

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1961年論文

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1961年論文

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1961年論文

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1961年论文

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name

DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

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DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

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DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

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DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

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DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

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DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

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DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

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DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

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Journal of Clinical Investigation

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DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

@en

P2093

Bauer CD

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Combes B

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De Bobes-Sternberg S

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Morell AG

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Schein-Berg IH

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Sternlier I

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P2860

Studies on copper metabolism. XIII. Hepatolenticular degeneration

Exchange of ceruloplasmin copper with ionic Cu64 with reference to Wilson's disease.

Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).

Genetic basis of the thalassaemia diseases.

Metabolic studies in Wilson's disease using Cu64.

Studies on copper metabolism. XIV. Radioactive copper studies in normal subjects and in patients with hepatolenticular degeneration.

Observations on ceruloplasmin in Wilson's disease.

Copper metabolism in normal adults and in clinically normal relatives of patients with Wilson's disease.

Sickle cell anemia, a molecular disease

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707-715

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scholarly article

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10.1172/JCI104304

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4

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40

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1961-04-01T00:00:00Z

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16695860

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290777

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