Results 71 to 80 of about 900 (164)

A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family

Hereditas
Congenital fibrinogen disorders are a group of coagulation deficiencies caused by fibrinogen defects and are divided into four types, including afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia, and hypodysfibrinogenemia. In this study, we collected
Xiaoying Xie, Juan Du, Shunkang Geng, Baoqin Yi, Qingpu Li, Jiangcheng Zuo   +5 more
doaj   +1 more source

Rapid laboratory identification of fibrinogen Longmont: a case report and literature review

Frontiers in Medicine
This study reports a case of a patient with unstable angina with abnormally low fibrinogen (FIB) levels detected during preoperative screening, yet whose clinical manifestations were markedly inconsistent with the test results.
Cuihua Ma, Xuezhuo Li, Da Yin, Huidong Ma, Wenran Lu, Chunhua Wang   +5 more
doaj   +1 more source

Laboratory investigation of thrombophilia [PDF]

Journal of Medical Biochemistry, 2014
Laboratory investigation of thrombophilia is aimed at detecting the well-established hereditary and acquired causes of venous thromboembolism, including activated protein C resistance/factor V Leiden mutation, prothrombin G20210A mutation, deficiencies ...
Margetić Sandra
doaj  

Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants

Haematologica, 2008
Background Congenital afibrinogenemia is characterized by the absence of fibrinogen, a hexamer composed of two copies of three polypeptides, Aα. Bβ and γ. The disease is caused by mutations in one of the three fibrinogen-encoding genes, FGA, FGB and FGG.
Dung Vu, Corinne Di Sanza, Marguerite Neerman-Arbez   +2 more
doaj   +1 more source

Relationship between the dual platelet‐inhibited ROTEM® Sigma FIBTEM assay and Clauss fibrinogen during postpartum haemorrhage

Anaesthesia, Volume 80, Issue 1, Page 104-106, January 2025.
Sarah F. Bell, Hazel Taylor, Philip Pallmann, Peter Collins, on behalf of the OBS Cymru collaborators (online Supporting Information Appendix S1)   +4 more
wiley   +1 more source

Severe haemorrhagic diathesis due to acquired hypofibrinogenemia in a patient with early T-cell precursor acute lymphoblastic leukaemia/lymphoma: a case report

Frontiers in Cardiovascular Medicine
The most frequent haematological malignancy associated with acquired hypo/dysfibrinogenemia is multiple myeloma. We present an unusual case of severe haemorrhagic diathesis due to acquired hypofibrinogenemia in a patient with early T-cell precursor acute
Luca Spiezia, Marcello Riva, Carmela Gurrieri, Elena Campello, Paolo Simioni   +4 more
doaj   +1 more source

Publication Only

HemaSphere, Volume 9, Issue S1, June 2025.
wiley   +1 more source

Management and outcomes of women with low fibrinogen concentration during pregnancy or immediately postpartum: A UK national population‐based cohort study

Acta Obstetricia et Gynecologica Scandinavica
Introduction Pregnant women with a fibrinogen level
Caroline Diguisto, Elfreda Baker, Simon Stanworth, Peter W. Collins, Rachel E. Collis, Marian Knight   +5 more
doaj   +1 more source

Dysfibrinogenemia [PDF]

, 2020
openaire   +1 more source

A Double Whammy of Mycotic Aneurysms and Acquired Dysfibrinogenemia in a Patient with Septicemia

Balkan Medical Journal, 2021
Chun Yang Sim, Ching Soong Khoo, Ruslinda Mustafar, Jia Ning Chai   +3 more
doaj   +1 more source