Results 131 to 140 of about 1,250 (185)

Rare inherited coagulation disorders: no longer orphan and neglected. [PDF]

Res Pract Thromb Haemost
Mohsenian S, Mannucci PM, Menegatti M, Peyvandi F.   +3 more
europepmc   +1 more source

Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework. [PDF]

J Thromb Haemost
Ross JE, Mohan S, Zhang J, Sullivan MJ, Bury L, Lee K, Futchi I, Frantz A, McDougal D, Perez Botero J, Cattaneo M, Cooper N, Downes K, Gresele P, Keenan C, Lee AI, Megy K, Morange PE, Morgan NV, Schulze H, Zimowski K, Freson K, Lambert MP.   +22 more
europepmc   +1 more source

Beta 2 adrenergic receptor polymorphisms: association with factor VIII and von Willebrand factor levels and the risk of venous thrombosis [PDF]

, 2005
Dai, L., Eikenboom, J.C.J., Nossent, A.Y., Rosendaal, F.R., Vos, H.L.   +4 more
core   +1 more source

A Review of Desmopressin Use in Bleeding Disorders: An Unsung Hero? [PDF]

Biomolecules
Reardon B, Pasalic L, Favaloro EJ.
europepmc   +1 more source

Laboratory and Clinical Analysis of Rare Coagulation Factor Deficiencies-A Respective Study of a Single Center from Northwest China. [PDF]

Clin Appl Thromb Hemost
Li J, Liu Y, Yuan L.
europepmc   +1 more source

Diagnosis, treatment, surgical practices and review of the literature in rare coagulation factor deficiencies. [PDF]

Ital J Pediatr
Solgun HA.
europepmc   +1 more source

Better with poorly performing fibrin(ogen).

Blood
Zhang L.
europepmc   +1 more source

About Congenital Afibrinogenemia.

Turkish journal of haematology : official journal of Turkish Society of Haematology, 2016
openaire   +1 more source

Some of the next articles are maybe not open access.

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Congenital afibrinogenemia

American Journal of Hematology, 1994
AbstractCongenital afibrinogenemia is a rare disorder with unusual clinical manifestations. The disease is inherited as an autosomal recessive trait and consanguinity is common among affected families. Clinical manifestations range from minimal bleeding to catastrophic hemorrhage.
H, al-Mondhiry, W C, Ehmann
exaly   +3 more sources

A case of congenital afibrinogenemia

Research in Clinic and Laboratory, 1983
A case of congenital afibrinogenemia is described. In the family studied, the defect is transmitted as an autosomal recessive trait. The possible heterogeneity of congenital afibrinogenemia is discussed.
A, Galletti, E, Barone, G, Gastaldi, A, Rasore Quartino   +3 more
exaly   +3 more sources