Results 141 to 150 of about 1,945 (206)

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

A Novel Fibrinogen Assay Using Recombinant Batroxobin and Carboxymethyl Chitosan: Carboxymethyl Chitosan Stimulates the Enzymatic Activity of Recombinant Batroxobin. [PDF]

Ann Lab Med
Kim JA, Ko E, Woo Y, Sohn YD, Kim JT, Song J, Park R.   +6 more
europepmc   +1 more source

P423: Recurrent pulmonary hemorrhages as a presenting symptom of congenital dysfibrinogenemia in a hospital patient identified from rapid whole genome sequencing

Genetics in Medicine Open
Rachel Hart, Pi Chun (Jennifer) Cheng, Kerry Hege, Brett Graham   +3 more
doaj   +1 more source

Acute obstetric coagulopathy is associated with excess plasmin generation and proteolysis of fibrinogen and factor V. [PDF]

Blood Adv
Collins PW, Whyte CS, de Lloyd L, Narwal A, Bell SF, Gill N, Collis RE, Jenkins PV, Mutch NJ.   +8 more
europepmc   +1 more source

Thrombocytosis and bleeding in myeloproliferative neoplasms: exploring clinical diversity and risk of acquired von Willebrand syndrome-insights from a UK center. [PDF]

Res Pract Thromb Haemost
Simini G, Innes A, Vinayagam S, Mobayen G, Karawitage N, Claudiani S, Odho Z, Laffan M, Arachchillage DJ.   +8 more
europepmc   +1 more source

[Congenital dysfibrinogenemia: current status and challenges in diagnosis and treatment]. [PDF]

Zhonghua Xue Ye Xue Za Zhi
Wang Z, Zhu TN.
europepmc   +1 more source

Factor XIII Deficiency: A Review of Biology, Testing, and Treatment. [PDF]

Clin Hematol Int
Jacobs JW, Booth GS, Costa V, Figueroa Villalba CA, Savani BN, Adkins BD.   +5 more
europepmc   +1 more source

Better with poorly performing fibrin(ogen).

Blood
Zhang L.
europepmc   +1 more source