(Q42730769)

5 November 2017

Successful treatment of homozygous protein C deficiency by hepatic transplantation (English)

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5 November 2017

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6

T E Starzl

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5 November 2017

J F Casella

1

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5 November 2017

J H Lewis

2

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5 November 2017

F A Bontempo

3

1 reference

5 November 2017

B J Zitelli

4

1 reference

5 November 2017

H Markel

5

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5 November 2017

language of work or name

English

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publication date

1 February 1988

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5 November 2017

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5 November 2017

1

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5 November 2017

8583

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5 November 2017

435-438

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Liver transplantation for advanced liver disease with alpha-1-antitrypsin deficiency

5 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Deficiency of protein C in congenital thrombotic disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Characterization of a cDNA coding for human protein C

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Severe inherited "homozygous" protein C deficiency in a newborn infant

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Congenital protein C deficiency and thrombotic disease in nine French families

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Familial protein S deficiency is associated with recurrent thrombosis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Heart-liver transplantation in a patient with familial hypercholesterolaemia

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Liver transplantation for type I glycogen storage disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Metabolic effects of hepatic replacement in Wilson's disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Liver transplantation in a hemophiliac

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Severe hereditary protein C deficiency in a newborn infant with fulminant purpura--successful treatment with phenprocoumon

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Neonatal purpura fulminans: a genetic disorder related to the absence of protein C in blood.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Indications for liver transplantation in the cyclosporine era.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Homozygous protein C deficiency: observations on the nature of the molecular abnormality and the effectiveness of warfarin therapy.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Liver transplantation in hemophilia A

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Orthotopic liver transplantation for type I Crigler-Najjar syndrome.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

The regulation of hemostasis: the protein C system

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Biosynthesis and secretion of factor VII, protein C, protein S, and the Protein C inhibitor from a human hepatoma cell line

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091362

Deficiencies of protein C, an inhibitor of blood coagulation

27 May 2018

1 reference

12 December 2020

Congenital protein C deficiency and venous thromboembolism. A study of three Dutch families

1 reference

12 December 2020

Protein C and the development of skin necrosis during anticoagulant therapy

1 reference

12 December 2020

Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant

1 reference

12 December 2020

Determination of functional levels of protein C, an antithrombotic protein, using thrombin-thrombomodulin complex

1 reference

12 December 2020

Homozygous protein C deficiency manifested by massive venous thrombosis in the newborn

1 reference

12 December 2020

Protein C deficiency in two Austrian families

1 reference

12 December 2020

The use of a functional and immunologic assay for plasma protein C in the study of the heterogeneity of congenital protein C deficiency

1 reference

12 December 2020

Coumarin necrosis associated with hereditary protein C deficiency

1 reference

12 December 2020

Severe homozygous protein C deficiency

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12 December 2020

Erythropoietic protoporphyria with hepatic cirrhosis

1 reference

12 December 2020

HEREDITARY DYSFUNCTIONAL PROTEIN C (PROTEIN C BERGAMO) AND THROMBOSIS

1 reference

12 December 2020

Hereditary protein C deficiency

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12 December 2020

Protein C in thromboembolic disease

1 reference

12 December 2020

An abnormal plasma distribution of protein S occurs in functional protein S deficiency

1 reference

12 December 2020

Purpura fulminans in a Chinese boy with congenital protein C deficiency

1 reference

12 December 2020

Resolution of the clinical features of tyrosinemia following orthotopic liver transplantation for hepatoma

1 reference

12 December 2020

1 reference

12 December 2020

Successful treatment of primary hyperoxaluria type I by combined hepatic and renal transplantation

1 reference

12 December 2020

1 reference

12 December 2020

10.1016/S0140-6736(88)91231-7

Identifiers

DOI

1 reference

5 November 2017

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5 November 2017

PubMed publication ID

2893866

1 reference