Results 111 to 120 of about 239,927 (172)

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 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  

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

Case Report: Co-Occurrence of Lung Adenocarcinoma and Congenital Dysfibrinogenemia-Diagnostic and Perioperative Management Challenges. [PDF]

Cancer Rep (Hoboken)
Zheng H, Wang Q, Wang M, Luo S, Ma Y, Wan Z.   +5 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

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

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

Factor XIII deficiency: an updated approach to diagnosis and management. [PDF]

Front Med (Lausanne)
Altahan RM.
europepmc   +1 more source