Results 101 to 110 of about 1,319 (189)

Platelet fibrinogen: subcellular localization by means of immunofluorescent studies in normals and in congenital afibrinogenemia.

, 1979
We have studied the site of fibrinogen localization in normal platelets and in the platelets of a patient with congenital afibrinogenemia (CA). The methods employed were: direct immunofluorescence technique (DIT) and indirect immunofluorescence technique
CASONATO, SANDRA, FABRIS, FABRIZIO, GIROLAMI, ANTONIO, BETTERLE, CORRADO   +3 more
core  

Rare Indications of Splenectomy: A Case Series and Literature Review. [PDF]

Cureus
Maran N, Chidambaranathan S, Moorthy K.
europepmc   +1 more source

Transfusion of fibrinogen concentrate before dental extractions in patients with afibrinogenemia: a narrative review supported by a case report with a proposed treatment protocol. [PDF]

Blood Transfus, 2023
Czajkowska S, Rupa-Matysek J, Brzezińska J, Surdacka A, Gil L.   +4 more
europepmc   +1 more source

Management of Hereditary Hypofibrinogenemia During Pregnancy: A Scoping Review Towards Personalized Obstetric Care. [PDF]

J Clin Med
Karampas G, Karkalemis K, Bagiasta A, Metallinou D, Tsarna E, Lefaki M, Staikou C, Eleftheriades M, Christopoulos P, Politou M.   +9 more
europepmc   +1 more source

Hypofibrinogenemia caused by a heterozygous variant in the FGA gene: a case report. [PDF]

Thromb J
Wei H, Yang X.
europepmc   +1 more source

Rare inherited autosomal bleeding disorders in women: sex-related bleeding, pregnancy and delivery. A narrative review. [PDF]

Blood Transfus
Martini T, Pollio B, Ricca I, Albiani R, Borsellino B.   +4 more
europepmc   +1 more source

Pharmacokinetics, Hemostatic Efficacy, and Safety of a New Human Fibrinogen Concentrate in Adult and Pediatric Patients with Congenital Fibrinogen Deficiency. [PDF]

Thromb Haemost
Djambas Khayat C, El-Beshlawy A, Meddeb B, Khelif A, Miesbach W, Adolf S, Boehm H, Aigner S, Abraha S, Bohlaender F, Schuettrumpf J.   +10 more
europepmc   +1 more source

Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database. [PDF]

Res Pract Thromb Haemost
Mohsenian S, Palla R, Menegatti M, Cairo A, Siboni SM, Neerman-Arbez M, Karimi M, Pargantou H, Asselta R, Mikovic D, Saracevic M, Laros-van Gorkom B, Jacobs L, Shapiro A, Williamson A, Makris M, Casini A, Peyvandi F.   +17 more
europepmc   +1 more source

P130 | LIVER TRANSPLANT IN CONGENITAL AFIBRINOGENEMIA: A CASE REPORT

Haematologica
Background: Fibrinogen (FBG) is involved in the final steps of coagulation as a precursor of fibrin monomers. Inherited FBG disorders are generally classified as quantitative or qualitative. Quantitative disorders include afibrinogenemia (aFBG), which is
G. Murante, S. Bergonzi, C. Sella, F. Valeri, C. Dainese, A. Valpreda, R. Pastorino, R. Romagnoli, D. Patrono, D. Cussa, S. Martini, B. Bruno, and A. Borchiellini   +12 more
doaj  

Bioinformatics analysis of the proteome in the pathway of complement and coagulation cascades in COVID-19: discovering potential biomarkers of FGB and SERPINA5. [PDF]

BMC Infect Dis
Liu S, Shi H, Yang Y, Zhu C, Zhou J, Jin W, Song S, Zhang L.   +7 more
europepmc   +1 more source