Results 111 to 120 of about 2,449 (204)

Perioperative coagulation management in a patient with afibrinogenemia undergoing liver transplantation [PDF]

, 2007
Ralph Fuchs, Jay M. Levin, Meghan Tadel, William T. Merritt   +3 more
openalex   +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

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

Existence of large Molecular Plasminogen Proactivator in Plasma from a Congenital Afibrinogenemia Patient

, 1971
U Okamoto, Masako Matsumoto
openalex   +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

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  

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

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

Targeted mutation of zebrafish fga models human congenital afibrinogenemia [PDF]

, 2014
Richard J. Fish, Corinne Di Sanza, Marguerite Neerman‐Arbez   +2 more
openalex   +1 more source