Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin (Q34283513)

1 August 2017

Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin (English)

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1 August 2017

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S. S. Shapiro

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5355338

6 May 2023

J. Martinez

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5355338

6 May 2023

R. R. Holburn

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5355338

6 May 2023

language of work or name

English

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publication date

1 December 1969

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full work available at URL

1 August 2017

https://europepmc.org/articles/PMC297482

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5355338

https://europepmc.org/articles/PMC297482?pdf=render

6 May 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5355338

Journal of Clinical Investigation

6 May 2023

published in

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1 August 2017

48

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1 August 2017

12

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1 August 2017

2251-2259

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Severe congenital hypoprothrombinemia in a Negro boy.

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Congenital hypofibrinogenemia in five members of a family

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

A study of a case of congenital hypoprothrombinaemia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

A modification for routine laboratory use of Stefanini's method of estimating factor V activity in human oxalated plasma

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Genetic variants of hemophilia B: detection by means of a specific PTC inhibitor

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

The immunologic character of acquired inhibitors of antihemophilic globulin (factor 8) and the kinetics of their interaction with factor 8.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Human prothrombin metabolism in normal man and in hypocoagulable subjects

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Genetics of human blood coagulation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Immunologic studies of antihemophilic factor (AHF, factor VIII): cross-reacting material in a genetic variant of hemophilia A.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

X-linked Recessive Inheritance in the Ehlers-Danlos Syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Congenital dysfibrinogenemia: fibrinogen detroit

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

An investigation of three patients with Christmas disease due to an abnormal type of factor IX.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Human prothrombin activation.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Plasma prothrombin during treatment with Dicumarol. II. Demonstration of an abnormal prothrombin fraction.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Some properties of purified prothrombin and its activation with sodium citrate.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Hemophilia A: polymorphism detectable by a factor 8 antibody

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Immunochemical Determination of Human Prothrombin

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Fibrinogen Detroit--a molecular defect in the N-terminal disulphide knot of human fibrinogen?

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

Inherited fibrinogen abnormality causing thrombophilia

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297482

28 October 2018

Genetic heterogeneity

1 reference

12 December 2020

[Mechanism of thrombin formation in the isolated system.]

1 reference

12 December 2020

Amino Acid Composition of Human Plasma Prothrombin

1 reference

12 December 2020

Chromatographic analysis of the activation of human prothrombin with human thrombokinase

1 reference

12 December 2020

Coagulation studies in four patients with Ehlers-Danlos syndrome

1 reference

12 December 2020

Study of a case of congenital hypoprothrombinemia

1 reference

12 December 2020

Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies

1 reference

12 December 2020

ANTI-FACTOR VIII CIRCULATING ANTICOAGULANTS DURING HEMOPHILIA A. (NATURE AND MECHANISM OF ACTION)

1 reference

12 December 2020

Chromatographic isolation of plasma prothrombin and t trans-alpha-glucosylase

1 reference

12 December 2020

Observations on the analysis for thrombin and the inactivation of fibrin monomer

1 reference

12 December 2020

Investigation of a haemorrhagic disease due to beta-prothromboplastin deficiency complicated by a specific inhibitor of thromboplastin formation

1 reference

12 December 2020

Congenital hypoprothrombinemic states

1 reference

12 December 2020

Enzyme and protein polymorphism in human populations

1 reference

12 December 2020

An inherited qualitative abnormality in plasma fibrinogen: fibrinogen Cleveland

1 reference

12 December 2020

Immunochemical studies on proteins important in blood coagulation

1 reference

12 December 2020

Hereditary hypoprothrombinaemias

1 reference

12 December 2020

A STUDY OF THREE CASES OF FAMILIAL CONGENITAL HYPOPROTHROMBINAEMIA (FACTOR II DEFICIENCY)

1 reference

12 December 2020

Familial Disturbance of Fibrin Monomer Aggregation

1 reference

12 December 2020

[A micro-method of immuno-electrophoresis]

1 reference

12 December 2020

A quick and accurate method for the determination of fibronogen in plasma

1 reference

12 December 2020

Preparation of human plasma prothrombin and some of its sedimentation properties

1 reference

12 December 2020

Antibodies to papain. A selective fractionation according to inhibitory capacity

1 reference

12 December 2020

[Immunologic study of human prothrombin and thrombin]

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI106191

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1 August 2017

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1 August 2017

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