Results 111 to 120 of about 1,319 (189)

Clotting Factor Deficiencies as an Underlying Cause of Abnormal Uterine Bleeding in Women of Reproductive Age: A Literature Review. [PDF]

Life (Basel), 2023
Livanou ME, Matsas A, Valsami S, Papadimitriou DT, Kontogiannis A, Christopoulos P.   +5 more
europepmc   +1 more source

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

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

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

Molecular Aspects of Rare Coagulation Factor Deficiencies. [PDF]

Cureus
Tourbih H, Harrach A, Bencharef H, Dehbi H, Oukkache B.   +4 more
europepmc   +1 more source

Afibrinogenemia

SEIBUTSU BUTSURI KAGAKU, 1967
openaire   +2 more sources

Congenital Afibrinogenemia With Facial Haematoma. [PDF]

Cureus
Hassan M, Khan M, Ghulam M, Anthony N, Khan M.   +4 more
europepmc   +1 more source

Spinal anesthesia in a patient with hereditary dysfibrinogenemia who underwent emergency cesarean delivery: a case report. [PDF]

JA Clin Rep
Ono S, Hosokawa Y, Kamiyama M, Ohsugi E, Gotanda M, Yamashita Y, Kato R.   +6 more
europepmc   +1 more source

A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations. [PDF]

Thromb J
Chen W, Hu J.
europepmc   +1 more source

Fibrinogen glycosylation and glycation: molecular insights into thrombosis and vascular disease. [PDF]

Front Mol Biosci
Borghi S, Nencini F, Giurranna E, Barbaro I, Taddei N, Fiorillo C, Becatti M.   +6 more
europepmc   +1 more source