Results 71 to 80 of about 1,945 (206)

Von Willebrand Disease: be or not to be, that is the question [PDF]

, 2015
Poster presented at the International Society on Thrombosis and Haemostasis 2015 Congress, 20-25 June 2015 ...
Azevedo, Ana, Fidalgo, Teresa, Freire, Isabel, Gago, Teresa   +3 more
core  

DYSFIBRINOGENEMIA IN BURNED CHILDREN [PDF]

Pediatric Research, 1989
Severely burned children often show a dysfunction of microcirculation, due to overproduction of O2 radicals and to the activation of blood coagulation. We studied the effect of H2O2 on fibrinogen collected from burned children. Controls were healthy adult donors. Fibrinogen was purified through precipitation with PEG and saltin-out procedure.
Domenico Del Principe, Adriana Menichelli, Massimo Giordani, Carlo M Colucci, Claudio Colistra, Stefano Di Giulio   +5 more
openaire   +1 more source

The Effect of Hepatitis B Infection on Levels of Fibrinogen, Protein C, and Protein S in Pregnant Women

Journal of Pregnancy, Volume 2026, Issue 1, 2026.
Background Viral hepatitis has been associated with profound alterations in the coagulation system as well as liver biomarkers. Meanwhile, during pregnancy, the coagulation system also undergoes significant changes with an increase in the majority of the clotting factors and a decrease in natural anticoagulants.
Abiba Alhassan Khalifah, Stephen Twumasi, Allwell Adofo Ayirebi, Wina Ivy Ofori Boadu, Francis Agyei Amponsah, Joseph Frimpong, David Amoah Afrifah, Ernest Appiagyei, Albert Ntim Boadu, Daniel Nii Martey Antonio, Enoch Odame Anto, Nidhi Chaudhary   +11 more
wiley   +1 more source

Heterozygous B beta-chain C-terminal 12 amino acid elongation variant, B beta X462W (Kyoto VI), showed dysfibrinogenemia [PDF]

, 2012
A heterozygous patient with dysfibrinogenemia with slight bleeding and no thrombotic complications was diagnosed with fibrinogen Kyoto VI (K-VI). To elucidate the genetic mutation(s) and characterize the variant protein, we performed the following ...
Fujita, Naohisa, Hirota-Kawadobora, Masako, Honda, Takayuki, Inaba, Tohru, Okumura, Nobuo, Saito, Masazumi, Sugano, Mitsutoshi, Takezawa, Yuka, Terasawa, Fumiko   +8 more
core   +1 more source

γD318Y fibrinogen shows no fibrin polymerization due to defective "A-a" and "B-b" interactions, whereas that of γK321E fibrinogen is nearly normal [PDF]

, 2019
ArticleThrombosis research. 182: 150-158.
Higuchi, yumiko, Kamijo, Tomu, Mukai, Saki, Okumura, Nobuo, Taira, Chiaki   +4 more
core   +1 more source

Diagnostic and management practices for inherited fibrinogen disorders: a nationwide survey of Italian Hemophilia Treatment Centers

Bleeding, Thrombosis and Vascular Biology
Background: inherited fibrinogen disorders are characterized by a spectrum of quantitative or qualitative fibrinogen deficiency associated with both a hemorrhagic and thrombotic risk.
Renato Marino, Silvia Linari, Marzia Leotta, Antonio Coppola, Chiara Biasoli, Maria Elisa Mancuso, Flora Peyvandi, Cristina Santoro, Ezio Zanon, Rita Carlotta Santoro   +9 more
doaj   +1 more source

Current Practice Regarding Bleeding Disorders of Unknown Cause in the Netherlands: A National Survey

Haemophilia, Volume 31, Issue 4, Page 752-760, July 2025.
ABSTRACT Introduction About 40%–70% of persons with a clinically relevant bleeding tendency who are referred to haemostasis experts are classified as having a ‘bleeding disorder of unknown cause’ (BDUC) as no biological entity can be found after extensive laboratory testing.
Caroline M. A. Mussert, Amaury L. L. Monard, Tirsa T. van Duijl, Yvonne M. C. Henskens, Maartje van den Biggelaar, Roger E. G. Schutgens, Saskia E. M. Schols, Karin J. Fijnvandraat, Karina Meijer, Paul L. den Exter, Laurens Nieuwenhuizen, Iris van Moort, Marieke J. H. A. Kruip, Marjon H. Cnossen, Floor C. J. I. Heubel‐Moenen, for the BDUC‐iN study group   +15 more
wiley   +1 more source

Современные подходы к имплантации кава-фильтров при угрозе тромбоэмболии легочных артерий [PDF]

, 2016
ТРОМБОЭМБОЛИЯ ЛЕГОЧНЫХ АРТЕРИЙПОСТТРОМБОФЛЕБИТИЧЕСКИЙ СИНДРОМТРОМБОЗ ВЕНОЗНЫЙСОСУДИСТАЯ ХИРУРГИЯКАВА ...
Глущенко, Л. В., Шарафеев, А. З.   +1 more
core  

Integrating Next‐Generation Sequencing Into Routine Molecular Diagnosis of Inherited Coagulation Factor Deficiencies: Real‐World Data From Spanish Patients

Haemophilia, Volume 31, Issue 4, Page 734-742, July 2025.
ABSTRACT Introduction Inherited coagulation factor deficiencies (ICFD) result from plasma protein deficiencies, impacting blood coagulation cascade and leading to haemorrhagic diathesis. Advancements in next‐generation sequencing (NGS) technology have enabled high‐throughput methods for molecular ICFD diagnosis.
Nina Borràs, Natàlia Comes, Lorena Ramírez, Rafael Parra, Carmen Altisent, Álvaro Lorenzo‐Vizcaya, Cristina Marzo‐Alonso, Maria‐Fernanda López‐Fernández, Mariana Canaro, María Falcón‐Rodríguez, Ángela Cortes‐Vidal, Mario A. Rios de Paz, José Antonio Rodríguez‐García, Ana Moreto‐Quintana, Perla Bandini, Carlos Hobeich, Irene Corrales, Francisco Vidal   +17 more
wiley   +1 more source

Congenital structural and functional fibrinogen disorders : a primer for internists [PDF]

, 2019
Congenital qualitative and quantitative fibrinogen disorders represent heterogeneous rare abnormalities caused by mutations in one of the 3 genes encoding individual fibrinogen polypeptide chains, located on chromosome 4q28.

core   +1 more source