Results 111 to 120 of about 760 (168)

[Congenital absolute afibrinogenemia].

Boletin medico del Hospital Infantil de Mexico, 1983
A, Bello-González, S, Dorantes, G, Ruiz-Reyes, J L, Márquez, A, Escanero, L, Loperena   +5 more
openaire   +1 more source

Multidisciplinary team management of congenital dysfibrinogenemia in pregnancy: a case report. [PDF]

BMC Pregnancy Childbirth
He MJ, Wei ZJ, Wang F, Zhang HY.
europepmc   +1 more source

Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. [PDF]

Blood Adv
Mohsenian S, Palla R, Menegatti M, Cairo A, Lecchi A, Casini A, Neerman-Arbez M, Asselta R, Scardo S, Siboni SM, Blatny J, Zapletal O, Schved JF, Giansily-Blaizot M, Halimeh S, Daoud MA, Platokouki H, Pergantou H, Schutgens REG, Van Haaften-Spoor M, Brons P, Laros-van Gorkom B, Van Pinxten E, Borhany M, Fatima N, Mikovic D, Saracevic M, Özdemir GN, Ay Y, Makris M, Lockley C, Mumford A, Harvey A, Austin S, Shapiro A, Williamson A, McGuinn C, Goldberg I, De Moerloose P, Peyvandi F.   +39 more
europepmc   +1 more source

An exploratory plasma-based functional assay for phenotypic characterization of fibrinolysis in dysfibrinogenemia. [PDF]

Res Pract Thromb Haemost
Suzuki A, Okamoto S, Suzuki N, Tamura S, Kanematsu T, Tomita M, Kojima T, Matsushita T.   +7 more
europepmc   +1 more source

A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia. [PDF]

Blood Coagul Fibrinolysis
Drotarova M, Asselta R, Caccia S, Skornova I, Zolkova J, Kolkova Z, Loderer D, Podusel V, Stasko J, Simurda T.   +9 more
europepmc   +1 more source

The fibrinogen αC region promotes arterial thrombosis in the context of hypofibrinogenemia.

Blood
Lee RH, Ferraresso F, Couzens A, Jameson AT, Hanes HE, Casini A, Neerman-Arbez M, Nieswandt B, Kastrup CJ, Bergmeier W, Flick MJ, Hur WS.   +11 more
europepmc   +1 more source

Highly thrombogenic phenotype and impaired wound healing in a patient with congenital dysfibrinogenemia: case report. [PDF]

Res Pract Thromb Haemost
El Beayni N, Szanto T, Neerman-Arbez M, Casini A, Lassila R.   +4 more
europepmc   +1 more source

[Clinical phenotypes and genotypes of congenital fibrinogen disorder: an analysis of 16 children]. [PDF]

Zhongguo Dang Dai Er Ke Za Zhi
Wang M, Chen TP, Jiang AS, Zhao YH, Zhu CL, Wei N, Jin YT, Qu LJ.   +7 more
europepmc   +1 more source

Rare inherited coagulation disorders: no longer orphan and neglected. [PDF]

Res Pract Thromb Haemost
Mohsenian S, Mannucci PM, Menegatti M, Peyvandi F.   +3 more
europepmc   +1 more source