(Q30448556)

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Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency

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1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency (English)

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

factor VII deficiency

1 reference

based on heuristic

inferred from title

author name string

HOUGIE C

1

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

BARROW EM

2

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

GRAHAM JB

3

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

language of work or name

0 references

publication date

1 March 1957

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

36

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

3

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

485-496

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Congenital SPCA deficiency: a hitherto unrecognized coagulation defect with hemorrhage rectified by serum and serum fractions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

20 June 2018

A familial hemorrhagic trait associated with a deficiency of a clot-promoting fraction of plasma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

20 June 2018

Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

20 June 2018

The thromboplastic activity of Russell's viper venom and its relationship to factor VII.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

20 June 2018

Haemorrhagic diathesis due to deficiency of factor VII

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

20 June 2018

Effect of antihemophilic factor on one-stage clotting tests; a presumptive test for hemophilia and a simple one-stage antihemophilic factor assy procedure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

20 June 2018

The thromboplastin generation test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

20 June 2018

Plasma thromboplastin component (PTC), a hitherto unrecognized blood coagulation factor; case report of PTC deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

20 June 2018

Plasma Thromboplastin Component (PTC) Deficiency Produced by Prolonged Administration of Prothrombopenic Anticoagulants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

26 November 2018

Congenital hemorrhagic diathesis of the prothrombin complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

26 November 2018

Newer approaches to the study of hemophilia and hemophilioid states

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

26 November 2018

Mild hemophilia; allelic form of the disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072666

26 November 2018

The purification of bovine antihaemophilic globulin

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital hypoproconvertinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemorrhagic diathesis due to a deficiency of factor VII (hypoproconvertinaemia)

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Constitutionally low blood levels of proconvertin]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Congenital hemorrhagic syndrome due to lack of the coagulation factor recently isolated under the name of factor 7, convertin, S.P.C.A. (congenital hemorrhagiparous hypoconvertinemia)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A case of congenital deficiency of factor VII (serum prothrombin conversion accelerator deficiency, congenital hypoproconvertinanemia)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mode of action of coumarin drugs

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoprothrombinemia; studies of a case of the idiopathic type and the effect of serum administration

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two cases of congenital hypoconvertinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Observations in congenital deficiency of factor VII (hypoconvertinemia)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new coagulation defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A case of congenital hypoconvertinemia]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple, specific one-stage prothrombin assay using Russell's viper venom in cephalin suspension

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Hemorrhagic diathesis due to deficiency of prothrombin conversion accelerator]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clotting factor X; physiologic and physico-chemical properties

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital hypoprothrombinemic states

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The coagulation defect caused by tromexan therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prothrombin and accessory factors; clinical significance

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intermediate stages in the formation of blood thromboplastin

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital familial deficiency of the stable prothrombin conversion factor; restudy of case originally reported as idiopathic hypoprothrombinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mild familial hypoproconvertinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that platelet accelerator (platelet factor 1) is adsorbed plasma proaccelerin

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Congenital factor VII (SPCA) deficiency as the cause of hemophilic-type hemorrhagic diathesis]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The initial stages of blood coagulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/13406063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI103446

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

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