Results 101 to 110 of about 239,927 (172)

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

Cureus
Maran N, Chidambaranathan S, Moorthy K.
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

Congenital afibrinogenemia. A case report and therapeutic trials

The Turkish Journal of Pediatrics, 1966
S Ozsoylu, C Altay, B Corbacioğlu
doaj  

Dysfibrinogenemia in Pregnancy: A Case Series Highlighting Diagnostic Challenges and Multidisciplinary Management. [PDF]

Cureus
Mahurkar S, Nnamani E, Lewis S, Parveen S.   +3 more
europepmc   +1 more source

Identification of genetic variants in the FGB gene associated with congenital hypofibrinogenemia with divergent clinical phenotype. [PDF]

Ann Hematol
Belakova KM, Asselta R, Caccia S, Kolkova Z, Loderer D, Drotarova M, Brunclikova M, Agouba SM, Gemelova VV, Stasko J, Mikler J, Simurda T.   +11 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

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

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

Novel variants require established frameworks: emphasizing the role of ISTH diagnostic and classification guidelines in congenital fibrinogen disorders. [PDF]

Hereditas
Bor MV.
europepmc   +1 more source