Results 111 to 120 of about 1,227 (170)

Targeted mutation of zebrafish fga models human congenital afibrinogenemia.

Blood, 2014
Fish RJ, Di Sanza C, Neerman-Arbez M.
europepmc   +1 more source

Bioinformatics analysis of the proteome in the pathway of complement and coagulation cascades in COVID-19: discovering potential biomarkers of FGB and SERPINA5. [PDF]

BMC Infect Dis
Liu S, Shi H, Yang Y, Zhu C, Zhou J, Jin W, Song S, Zhang L.   +7 more
europepmc   +1 more source

Kamus Obstetri dan Ginekologi [PDF]

, 1993
Iswati, Ellya, Jacob, Teuku Zulkifli, Rachimhadi, Trijatmo, Saifuddin, Abdul Bari   +3 more
core  

Novel variants require established frameworks: emphasizing the role of ISTH diagnostic and classification guidelines in congenital fibrinogen disorders. [PDF]

Hereditas
Bor MV.
europepmc   +1 more source

A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations. [PDF]

Thromb J
Chen W, Hu J.
europepmc   +1 more source

Congenital afibrinogenemia. A case report and therapeutic trials

The Turkish Journal of Pediatrics, 1966
S Ozsoylu, C Altay, B Corbacioğlu
doaj  

Molecular Aspects of Rare Coagulation Factor Deficiencies. [PDF]

Cureus
Tourbih H, Harrach A, Bencharef H, Dehbi H, Oukkache B.   +4 more
europepmc   +1 more source

Hypofibrinogenemia : a problem in obstetrics [PDF]

, 1957
Haroothunian, Edick
core   +1 more source

Clinical and Genetic Characterization of 51 Patients with Congenital Fibrinogen Disorders from China. [PDF]

Thromb Haemost
Cai Y, Lu H, Lin W, Xia Y, Wu T, Cheng Z, Tang LV, Hu Y.   +7 more
europepmc   +1 more source

Fibrinogen glycosylation and glycation: molecular insights into thrombosis and vascular disease. [PDF]

Front Mol Biosci
Borghi S, Nencini F, Giurranna E, Barbaro I, Taddei N, Fiorillo C, Becatti M.   +6 more
europepmc   +1 more source