(Q45856466)

English

Congenital combined factor V and factor VIII deficiency in a male born from a brother-sister incest

scientific article published in January 1974

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

Congenital combined factor V and factor VIII deficiency in a male born from a brother-sister incest (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

author name string

A Girolami

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

A Brunetti

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

L De Marco

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

publication date

1 January 1974

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

28

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

33-42

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

MEASUREMENT OF PLATELET ADHESIVENESS. A SIMPLE IN VITRO TECHNIQUE DEMONSTRATING AN ABNORMALITY IN VON WILLEBRAND'S DISEASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Congenital factor V deficiency (parahemophilia) with true hemophilia in two brothers]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Observations on hemophilia, parahemophilia, and coexistent hemophilia and parahemophilia; alterations in the platelets and the thromboplastin generation test.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant agains

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A report of a case of congenital afibrinogenemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined Deficiency of Factor V and Factor VIII (Antihaemophilic Globulin): A REPORT OF THREE CASES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parahemophilia. A case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A method for the study of antihaemophilic globulin inhibitors with reference to six cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined Factor-V and Factor- VIII Deficiency: Report of Four Cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of human blood coagulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital hypoprothrombinemia. Case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital familial deficiency of factor V (parahaemophilia) combined with deficiency of antihaemophilic globulin

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital combined deficiency of factor 8 (antihaemophilic globulin) and factor V (proaccelerin) in two siblings. Clinical study and genetic speculations

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of exercise on the level of antihaemophilic globulin in human blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/4810902

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01630657

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/4810902

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