Recurrent ischemic cerebrovascular events in a patient with type I antithrombin deficiency caused by 9788 G>A splice site mutation-Reference-Cited by-同舟云学术

Recurrent ischemic cerebrovascular events in a patient with type I antithrombin deficiency caused by 9788 G>A splice site mutation

Published:2013-03 Issue:2 Volume:24 Page:213-215
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Szymańska Magdalena,Alhenc-Gelas Martine,Undas Anetta

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

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3. Ischemic stroke due to deficiency of coagulation inhibitors. Report of 10 young adults.;Martinez;Stroke,1993

4. Molecular genetics of human antithrombin deficiency.;Perry;Hum Mutat,1996

5. Impact of thrombophilia on risk of arterial ischemic stroke or cerebral sinovenous thrombosis in neonates and children: a systematic review and meta-analysis of observational studies.;Kenet;Circulation,2010

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