(Q45888747)

English

Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients

scientific article published in July 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

0 references

coagulation factor x human

1 reference

based on heuristic

factor X deficiency

1 reference

based on heuristic

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

Pier Mannuccio Mannucci

2

object named as

Mannucci PM

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

author name string

Lak M

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

Abdoullahi M

4

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

Zeinali S

5

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

Sharifian R

6

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

Perry D

7

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

language of work or name

0 references

publication date

1 July 1998

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

British Journal of Haematology

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

102

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

626-628

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00806.X

21 January 2018

Factor X and its deficiency states

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00806.X

21 January 2018

Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00806.X

21 January 2018

Identifiers

10.1046/J.1365-2141.1998.00806.X

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

release_v4ld3brtbrhrlhq2kxqpy2tjsi

1 reference

https://api.fatcat.wiki/v0/release/v4ld3brtbrhrlhq2kxqpy2tjsi

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/9695984

ResearchGate publication ID

0 references

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