Results 101 to 110 of about 760 (168)

Rare inherited autosomal bleeding disorders in women: sex-related bleeding, pregnancy and delivery. A narrative review. [PDF]

Blood Transfus
Martini T, Pollio B, Ricca I, Albiani R, Borsellino B.   +4 more
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  

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

Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database. [PDF]

Res Pract Thromb Haemost
Mohsenian S, Palla R, Menegatti M, Cairo A, Siboni SM, Neerman-Arbez M, Karimi M, Pargantou H, Asselta R, Mikovic D, Saracevic M, Laros-van Gorkom B, Jacobs L, Shapiro A, Williamson A, Makris M, Casini A, Peyvandi F.   +17 more
europepmc   +1 more source

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

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

Congenital afibrinogenemia diagnosis by estimating plasma fibrinogen by conventional method with clinical correlation

Indian Journal of Pathology and Microbiology, 2008
Goswami K, Nandakumar Dalavaikodihalli, Soundravally R, Nandeesha H, Das Vanitalal, Kannan R, Nalini P, Koner B   +7 more
doaj  

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