Results 101 to 110 of about 5,300 (203)

Urticaria, Fever, and Hypofibrinogenemia [PDF]

Arthritis & Rheumatology, 2014
Verena, Mohr, Ansgar, Schulz, Peter, Lohse, Christian, Schumann, Klaus-Michael, Debatin, Catharina, Schuetz   +5 more
openaire   +2 more sources

Congenital hypofibrinogenemia.

Indian pediatrics, 2004
Congenital afibrinogenemia/hypofibrinogenemia is an extremely rare coagulation disorder. We describe a case of congenital hypofibrinogenemia in a 6-year female child, who presented with recurrent ecchymotic spots with no frank bleeding.
Neeraj, Awasthy, K C, Aggarwal, H, Gupta, S, Saluja   +3 more
openaire   +1 more source

Tigecycline-associated hypofibrinogenemia: A single center, retrospective, controlled study

Background: Tigecycline-associated hypofibrinogenemia has been reported as an important adverse effect in recent years, but controlled studies minimizing confounding factors are needed.
İNKAYA, AHMET ÇAĞKAN, FIRAT, OĞUZHAN, KARA, EMRE, Demirkan, Kutay, MALKAN, ÜMİT YAVUZ   +4 more
core   +1 more source

Congenital hypofibrinogenemia : characterization of two missense mutations affecting fibrinogen assembly and secretion

, 2008
Congenital hypofibrinogenemia is a rare bleeding disorder characterized by abnormally low levels of fibrinogen in plasma, generally due to heterozygous mutations in one of the three fibrinogen genes (FGA, FGB, and FGG, coding for Aalpha, Bbeta, and gamma
M.L. Tenchini, S. Spena, S. Duga, M. Spreafico, M. Platè, S. Fagoonee, R. Asselta, F. Peyvandi   +7 more
core   +1 more source

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

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

A Case Report of Crotalidae Immune F(ab’)2-associated Coagulopathy Recurrence in a Preschool-age Child

Clinical Practice and Cases in Emergency Medicine
Introduction: Pit viper envenomation may cause coagulopathy. The coagulopathy has been treated with crotalidae polyvalent immune fragment antigen-binding (Fab) ovine antivenom for the last few decades in the United States and usually corrects the acute ...
Jean C.Y. Lo, E. Lea Walters, Brian Wolk
doaj   +1 more source

Clinical Significance of Rotational Thromboelastometry (ROTEM) for Detection of Early Coagulopathy in Trauma Patients: A Retrospective Study

Diagnostics
Background: We aimed to evaluate the clinical significance of abnormal rotational thromboelastometry (ROTEM) findings in trauma patients and investigate the relationships between FIBTEM-maximum clot firmness (MCF), fibrinogen concentration and patient ...
Mohammad Asim, Ayman El-Menyar, Ruben Peralta, Suresh Arumugam, Bianca Wahlen, Khalid Ahmed, Naushad Ahmad Khan, Amani N. Alansari, Monira Mollazehi, Muhamed Ibnas, Ammar Al-Hassani, Ashok Parchani, Talat Chughtai, Sagar Galwankar, Hassan Al-Thani, Sandro Rizoli   +15 more
doaj   +1 more source

Congenital hypofibrinogenemia with bone cyst: a case report with review of literature

Congenital hypofibrinogenemia is a rare autosomal recessive condition leading to low plasma fibrinogen levels, affecting approximately one in a million.
Yelugoti, V, Mamadapur, M
core