Results 141 to 150 of about 2,449 (204)

Diagnosis, treatment, surgical practices and review of the literature in rare coagulation factor deficiencies. [PDF]

Ital J Pediatr
Solgun HA.
europepmc   +1 more source

Afibrinogenemia: Case Series of Rare Inherited Bleeding Disorder

, 2018
Neena Phade, Kriti Hegde, Vaibhav Shah, Prakruthi Kaushik, Arpita Gupta, Nikita Shah, Purvi Kadakia, Sujata Sharma, Radha Ghildiyal   +8 more
openalex   +1 more source

Integrating Next-Generation Sequencing Into Routine Molecular Diagnosis of Inherited Coagulation Factor Deficiencies: Real-World Data From Spanish Patients. [PDF]

Haemophilia
Borràs N, Comes N, Ramírez L, Parra R, Altisent C, Lorenzo-Vizcaya Á, Marzo-Alonso C, López-Fernández MF, Canaro M, Falcón-Rodríguez M, Cortes-Vidal Á, Rios de Paz MA, Rodríguez-García JA, Moreto-Quintana A, Bandini P, Hobeich C, Corrales I, Vidal F.   +17 more
europepmc   +1 more source

Association between factor I fibrinogen (rs6050) and factor XI plasma thromboplastin (rs4253417) genetic polymorphisms and recurrent spontaneous miscarriage in Saudi women. [PDF]

Saudi Med J
Kaabi AM, Alkhuriji AF, Babay ZA, Barakat IA, Kaabi AM, Kaabi RM.   +5 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

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

Better with poorly performing fibrin(ogen).

Blood
Zhang L.
europepmc   +1 more source

Late Intracerebral Hemorrhage After Successful Endovascular Closure of a Carotid-Cavernous Fistula: A Case Report and Updated Review. [PDF]

Reports (MDPI)
Uscamaita K, Pla MG, Terceño M, Arboix A, Silva Y.   +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  

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