(Q50901919)

English

[Homozygous infant in a family with hereditary protein C deficiency].

scientific article published in July 1987

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

[Homozygous infant in a family with hereditary protein C deficiency]. (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

1 reference

based on heuristic

inferred from title

author name string

G Hintz

1

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

J Weil

2

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

S Buchmann

3

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

A Azzam

4

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

K Auberger

5

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

C Beck

6

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

language of work or name

0 references

publication date

1 July 1987

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

Klinische Wochenschrift

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

65

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

12

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

576-580

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new vitamin K-dependent protein. Purification from bovine plasma and preliminary characterization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe homozygous protein C deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein C deficiency in Austria

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of an endothelial cell cofactor for thrombin-catalyzed activation of protein C.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The regulation of hemostasis: the protein C system

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship of "new" vitamin K-dependent Protein C and "old" autoprothrombin II-a

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of protein C in congenital thrombotic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inhibition of blood coagulation by activated protein C through the selective inactivation of activated factor V

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of action of human activated protein C, a thrombin-dependent anticoagulant enzyme

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of purified prothrombin to autoprothrombin I or autoprothrombin II (platelet cofactor II or autoprothrombin II-A).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3626426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01727627

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/3626426

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