(Q30448554)

5 November 2017

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

1 reference

5 November 2017

GRAHAM JB

1

1 reference

5 November 2017

BARROW EM

series ordinal

2

1 reference

5 November 2017

HOUGIE C

series ordinal

3

1 reference

5 November 2017

language of work or name

English

0 references

publication date

1 March 1957

1 reference

Journal of Clinical Investigation

5 November 2017

1 reference

5 November 2017

36

1 reference

5 November 2017

3

1 reference

5 November 2017

497-503

1 reference

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

5 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

Biochemical genetics of blood coagulation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

Haemorrhagic diathesis due to deficiency of factor VII

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

The thromboplastin generation test

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

A familial disorder of blood coagulation due to deficiency of the labile factor.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

Assay of plasma antihemophilic activity in normal heterozygous (hemophilia) and prothrombinopenic dogs

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

Variable manifestations of plasma thromboplastin component deficiency

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

Congenital hemorrhagic diathesis of the prothrombin complex

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

Mild hemophilia; allelic form of the disease.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1072667

Congenital hypoproconvertinemia

26 November 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

Two cases of congenital hypoconvertinemia

1 reference

12 December 2020

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

1 reference

12 December 2020

A new coagulation defect

1 reference

12 December 2020

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

1 reference

12 December 2020

Congenital hypoprothrombinemic states

1 reference

12 December 2020

Familial factor V deficiency: the pattern of heredity

1 reference

12 December 2020

A coagulation disorder due to a factor VII-like defect

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI103447

1 reference

5 November 2017

1 reference

5 November 2017

PubMed publication ID

13406064

1 reference