Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutation.

about

Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed.

P2860

Q53132506-09BC8ADD-18F1-4B71-8BDB-C8D90A6AF5C3

P2860

Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutation.

Item

http://www.wikidata.org/entity/Q51263915

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

Paradoxical bleeding and throm ...... homozygous Arg382His mutation.

@en

Paradoxical bleeding and throm ...... homozygous Arg382His mutation.

@nl

type

Item

label

Paradoxical bleeding and throm ...... homozygous Arg382His mutation.

@en

Paradoxical bleeding and throm ...... homozygous Arg382His mutation.

@nl

prefLabel

Paradoxical bleeding and throm ...... homozygous Arg382His mutation.

@en

Paradoxical bleeding and throm ...... homozygous Arg382His mutation.

@nl

P1476

Paradoxical bleeding and throm ...... homozygous Arg382His mutation.

@en

P2093

Alireza R Rezaie

http://www.w3.org/2001/XMLSchema#string

Likui Yang

http://www.w3.org/2001/XMLSchema#string

Qiulan Ding

http://www.w3.org/2001/XMLSchema#string

Wenman Wu

http://www.w3.org/2001/XMLSchema#string

Xiaoqing Zhao

http://www.w3.org/2001/XMLSchema#string

Xuefeng Wang

http://www.w3.org/2001/XMLSchema#string

P2860

Protein C Thr315Ala variant results in gain of function but manifests as type II deficiency in diagnostic assays

Platelet polyphosphates are proinflammatory and procoagulant mediators in vivo

The refined 1.9 A crystal structure of human alpha-thrombin: interaction with D-Phe-Pro-Arg chloromethylketone and significance of the Tyr-Pro-Pro-Trp insertion segment

The cytoprotective protein C pathway

TAFI, or plasma procarboxypeptidase B, couples the coagulation and fibrinolytic cascades through the thrombin-thrombomodulin complex

The molecular basis of blood coagulation

The dynamics of thrombin formation

Transglutaminase factor XIII uses proteinase-like catalytic triad to crosslink macromolecules.

Rare coagulation disorders.

Hereditary prothrombin deficiency presenting as intracranial haematoma in infancy.

P304

479-490

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1160/TH16-10-0750

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

117

http://www.w3.org/2001/XMLSchema#string

P577

2016-12-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27975099

http://www.w3.org/2001/XMLSchema#string

P932

5330935

http://www.w3.org/2001/XMLSchema#string

Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutation.

about

P2860

P2860

Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932