Results 121 to 130 of about 1,912 (211)

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

Endovascular Treatment for Lower-extremity Arterial Thrombosis in a Patient with Congenital Afibrinogenemia and a History of Bleeding Complications. [PDF]

Intern Med, 2022
Hiramatsu D, Ogihara Y, Matsumoto T, Sato K, Takasaki A, Kurita T, Okamoto R, Wada H, Dohi K.   +8 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

Extension of the Human Fibrinogen Database with Detailed Clinical Information-The αC-Connector Segment. [PDF]

Int J Mol Sci, 2021
Sovova Z, Pecankova K, Majek P, Suttnar J.   +3 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

Hemorragias por incoagulabilidad en Obstetricia y Cirugía [PDF]

, 1963
Mateu-Aragonés, José Mª, Usandizaga, J. A.   +1 more
core  

Congenital Afibrinogenemia With Facial Haematoma. [PDF]

Cureus
Hassan M, Khan M, Ghulam M, Anthony N, Khan M.   +4 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  

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