Results 121 to 130 of about 1,246 (182)

The fibrinogen αC region promotes arterial thrombosis in the context of hypofibrinogenemia.

Blood
Lee RH, Ferraresso F, Couzens A, Jameson AT, Hanes HE, Casini A, Neerman-Arbez M, Nieswandt B, Kastrup CJ, Bergmeier W, Flick MJ, Hur WS.   +11 more
europepmc   +1 more source

Trauma-induced dysfibrinogenemia: the von Clauss assay does not accurately measure fibrinogen levels after injury. [PDF]

Blood Vessel Thromb Hemost
DeBot M, Erickson C, Schaid T, LaCroix I, Moore EE, Silliman C, Cohen MJ, D'Alessandro A, Hansen KC.   +8 more
europepmc   +1 more source

Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. [PDF]

Blood Adv
Mohsenian S, Palla R, Menegatti M, Cairo A, Lecchi A, Casini A, Neerman-Arbez M, Asselta R, Scardo S, Siboni SM, Blatny J, Zapletal O, Schved JF, Giansily-Blaizot M, Halimeh S, Daoud MA, Platokouki H, Pergantou H, Schutgens REG, Van Haaften-Spoor M, Brons P, Laros-van Gorkom B, Van Pinxten E, Borhany M, Fatima N, Mikovic D, Saracevic M, Özdemir GN, Ay Y, Makris M, Lockley C, Mumford A, Harvey A, Austin S, Shapiro A, Williamson A, McGuinn C, Goldberg I, De Moerloose P, Peyvandi F.   +39 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

Pregnancy management for patients with bleeding disorders. [PDF]

Hematology Am Soc Hematol Educ Program
Patel N, Bannow BS.
europepmc   +1 more source

Clinical phenotype and laboratory characteristics of 93 patients with congenital fibrinogen disorders from unrelated 36 families. [PDF]

Res Pract Thromb Haemost
Tian D, Liang J, Gao H, Xu X, Nie W, Yin M, Lou J, Shen HQ.   +7 more
europepmc   +1 more source

Bloodless Surgeries in Pediatric Dentistry: A Review. [PDF]

J Pharm Bioallied Sci
Aggarwal N, Rana V, Srivastava N, Kaushik N, Kaur N.   +4 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

Chronic thromboembolic pulmonary hypertension: towards an etiology-oriented conceptual framework. [PDF]

Front Med (Lausanne)
Nishiyama M, Okada T, Teranaka W, Naruko T, Koyama T.   +4 more
europepmc   +1 more source

Sneddon Syndrome revealing dysfibrinogenemia

International Journal of Dermatology, 2003
Sneddon syndrome (SS) is the association of cerebral ischemic events and livedo and is caused by vascular thrombosis. It is often associated with a primitive antiphospholipid syndrome (PAPS). In other cases, several thrombophilic conditions have been implicated. Dysfibrinogenemia is a qualitative defect of fibrinogen.
Khosrotehrani, Kiarash, Leroy-Matheron, Catherine, Mourier, Claude, Revuz, Jean, Bagot, Martine   +4 more
openaire   +6 more sources