Literature DB >> 21725578

Two different fibrinogen gene mutations associated with bleeding in the same family (A αGly13Glu and γGly16Ser) and their impact on fibrin clot properties: fibrinogen Krakow II and Krakow III.

Danuta Pietrys, Walentyna Balwierz, Teresa Iwaniec, Silja Vorjohann, Marguerite Neerman-Arbez, Anetta Undas.   

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Year:  2011        PMID： 21725578     DOI： 10.1160/TH11-02-0102

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN： 0340-6245            Impact factor:   5.249


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  3 in total

1.  Combined use of Clauss and prothrombin time-derived methods for determining fibrinogen concentrations: Screening for congenital dysfibrinogenemia.

Authors:  Liqun Xiang; Meiling Luo; Jie Yan; Lin Liao; Weijie Zhou; Xuelian Deng; Donghong Deng; Peng Cheng; Faquan Lin
Journal:  J Clin Lab Anal       Date:  2017-09-18       Impact factor: 2.352

2.  Case Report: Unmasked Inherited Dysfibrinogenemia After Everolimus Therapy.

Authors:  Alona A Merkulova; Steven C Mitchell; Sergei Merkulov; Alisa S Wolberg; Marguerite Neerman-Arbez; Alvin H Schmaier
Journal:  Front Med (Lausanne)       Date:  2020-11-27

Review 3.  Extension of the Human Fibrinogen Database with Detailed Clinical Information-The αC-Connector Segment.

Authors:  Zofie Sovova; Klara Pecankova; Pavel Majek; Jiri Suttnar
Journal:  Int J Mol Sci       Date:  2021-12-23       Impact factor: 5.923
  3 in total

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