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Neurological Sciences
Published in: Neurological Sciences 8/2020

01-08-2020 | Dabigatran | Letter to the Editor

Cortical venous thrombosis, multiple cortical infarctions, and vaginal bleeding in a Chinese family with hypofibrinogenemia caused by the FGG mutation c.1019C>T: a case report

Authors: Hongbing Nie, Xiangbin Wu, Bing Bao, Zhongbin Xia, Dandan Tan

Published in: Neurological Sciences | Issue 8/2020

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Excerpt

Dear Editor, …
Literature
1.
Shapiro SE, Phillips E, Manning RA, Morse CV, Murden SL, Laffan MA, Mumford AD (2013) Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia. Br J Haematol 160(2):220–227CrossRef
2.
Côté HC, Lord ST, Pratt KP (1998) Gamma-chain dysfibrinogenemias: molecular structure-function relationships of naturally occuring mutations in the gamma chain of human fibrinogen. Blood 92(7):2195–2212CrossRef
3.
Malli L, Khan S, Qeadan F, Ismail M, Ramaswamy D, Hedna VS (2017) Cerebral venous thrombosis: continental disparities. Neurol Sci 38(11):1963–1968CrossRef
4.
Diamanti S, Longoni M, Agostoni EC (2019) Leading symptoms in cerebrovascular diseases: what about headache? Neurol Sci 40(Suppl 1):147–152CrossRef
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Niwa K, Mimuro J, Miyata M, Sugo T, Ohmori T, Madoiwa S, Tei C, Sakata Y (2008) Dysfibrinogen Kagoshima with the amino acid substitution gamma Thr-314 to Ile: analyses of molecular abnormalities and thrombophilic nature of this abnormal molecule. Thromb Res 121(6):773–780CrossRef
Metadata
Title
Cortical venous thrombosis, multiple cortical infarctions, and vaginal bleeding in a Chinese family with hypofibrinogenemia caused by the FGG mutation c.1019C>T: a case report
Authors
Hongbing Nie
Xiangbin Wu
Bing Bao
Zhongbin Xia
Dandan Tan
Publication date
01-08-2020
Publisher
Springer International Publishing
Published in
Neurological Sciences / Issue 8/2020
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI
https://doi.org/10.1007/s10072-020-04346-0

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