Results 161 to 170 of about 1,945 (206)

[Dysfibrinogenemia. A new case: dysfibrinogenemia Giessen III (author's transl)].

Klinische Wochenschrift, 1977
A new case of dysfibrinogenemia is reported which shows no signs of a haermorrhagic diathesis (dysfibrinogenemia Giessen III). The abnormal fibrinogen was detected by only slight but characteristic alterations of some parameter of the coagulation analysis (prolonged clotting times after addition of thrombin, Reptilase and thrombin coagulase; low ...
F R, Matthias, W H, Krause, S, Ganssert, K, Mueller, H G, Lasch   +4 more
openaire   +1 more source

Dysfibrinogenemia and thrombosis.

Nouvelle revue francaise d'hematologie, 1992
A thrombotic tendency (venous or arterial) has been reported in some cases of dysfibrinogenemia. We report here the mechanism by which these thrombosis may occur. It may be related either to a defective clot lysis due to a poor reactivity toward fibrinolytic enzymes or to a defective thrombin binding capacity of the abnormal clot.
J, Soria, C, Soria, J P, Collet, M, Mirishahi, H, Lu, J P, Caen   +5 more
openaire   +1 more source

Congenital Dysfibrinogenemias

Annals of Internal Medicine, 1972
H R, Gralnick, J S, Finlayson
openaire   +2 more sources

Thrombotic Dysfibrinogenemia

Thrombosis Research, 2000
Rita Marchi, Shah Soltan Mirshahi, Claudine Soria, Manouchehr Mirshahi, Mishal Zohar, Jean Philippe Collet, Norma B. de Bosch, Carmen Luisa Arocha-Piñango, Jeannette Soria   +8 more
openaire   +1 more source

Dysfibrinogenemia and placental abruption

Obstetrics & Gynecology, 2000
R Z, Edwards, A, Rijhsinghani
openaire   +2 more sources

Acute obstetric coagulopathy during postpartum hemorrhage is caused by hyperfibrinolysis and dysfibrinogenemia: an observational cohort study

Journal of Thrombosis and Haemostasis, 2023
Lucy de Lloyd, Nicola J Mutch
exaly  

[Obstetrical management in dysfibrinogenemia].

Geburtshilfe und Frauenheilkunde, 1990
Dysfibrinogenaemia is an inherited disorder, characterised by a plasmafibrinogen in normal concentration, but of abnormal quality due to impaired release of fibrinopeptides and/or impaired aggregation of fibrinomonomers. The typical abnormalities of the laboratory findings will be demonstrated by presenting the case reports of 4 patients with 5 ...
H, Heidegger, M, Spannagel, W, Schramm
openaire   +1 more source

Fibrinogen and dysfibrinogenemia.

Annals of clinical and laboratory science, 1981
The fibrinogen molecule is becoming increasingly understood. Amino acid sequencing has been undertaken and studies of abnormal fibrinogens are leading to a more functional concept of its structure. Acquired dysfibrinogenemia appears to be a more common problem than previously thought, and may be found in patients with liver disease, cancer ...
openaire   +1 more source

Congenital dysfibrinogenemia in major surgery: A description of four cases and review of the literature

Clinica Chimica Acta, 2022
Fa-Quan Lin
exaly  

Dysfibrinogenemia as Thrombophilic Factor

1992
The prevalence of congenital disfibrinogenemia in venous thrombosis is approximately 0.5% as deduced from 5 studies on familial thrombophilia including a total of 1871 patients [1-5]. This is low in comparison with the prevalence of deficiencies of anticoagulation factors such as antithrombin III protein S and protein C, which together account for one ...
openaire   +1 more source