A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred-Reference-Cited by-同舟云学术

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

Published:1970-08 Issue:2 Volume:19 Page:179-192
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Girolami A.,Molaro G.,Lazzzarin M.,Scarpa R.,Brunetti A.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1970.tb01615.x/fullpdf

Reference44 articles.

1. A New Inherited Coagulation Disorder Caused by an Abnormal Fibrinogen (‘Fibrinogen Baltimore’)

Cited by 153 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The slow but progressive disappearance of the patients with the Pro343Ser (FX Friuli) mutation;British Journal of Haematology;2020-08-04

2. Factor X Deficiency Due to a Compound Heterozygosis Between a New Mutation (Gla72Asp) in Exon 2 and an Already Known one (Gly154Arg) in Exon 5: Factor X Mar Del Plata1);Cardiovascular & Hematological Disorders-Drug Targets;2019-07-05

3. Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period;Journal of Thrombosis and Thrombolysis;2019-01-29

4. New data on FII, FV, FIX and thrombomodulin defects: blood keeps clotting in normal and in peculiar ways;Hematology;2018-12-15

5. New clotting disorders that cast new light on blood coagulation and may play a role in clinical practice;Journal of Thrombosis and Thrombolysis;2017-03-01

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