Results 121 to 130 of about 1,227 (170)

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

[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 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  

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

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

A familial study of a de novo FGG gene mutation causing congenital hypofibrinogenaemia and intervention during pregnancy and childbirth. [PDF]

Sci Rep
Xie Z, Li H, Guo Y, Mao B, Wang J, Gao M, Ma X.   +6 more
europepmc   +1 more source

Beta 2 adrenergic receptor polymorphisms: association with factor VIII and von Willebrand factor levels and the risk of venous thrombosis [PDF]

, 2005
Dai, L., Eikenboom, J.C.J., Nossent, A.Y., Rosendaal, F.R., Vos, H.L.   +4 more
core   +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