Results 141 to 150 of about 1,246 (182)

Congenital dysfibrinogenemia : Fibrinogen lille

Thrombosis Research, 1978
A dysfibrinogenemia (fibrinogen Lille) was detected in a 6 year old girl with no history of unusual bleeding. Thrombin and batroxobin (“reptilase”) times were markedly prolonged. The plasma fibrinogen level was unmeasurable by a kinetic method (Clauss), whereas normal values were obtained by immunochemical (Laurell) and gravimetric (Ingram) assays ...
M H, Denninger, J S, Finlayson, L A, Reamer, A, Parquet-Gernez, M, Goudemand, D, Menache   +5 more
openaire   +2 more sources

Management of pregnancy in dysfibrinogenemia cases

Blood Coagulation & Fibrinolysis, 2017
Dysfibrinogenemia is a very challenging disorder, and there are no firm guidelines on treatment for pregnant patients with dysfibrinogenemia. A 37-year-old patient with a history of six unexplained recurrent miscarriages was referred for thrombophilia testing.
Rucha, Patil, Alfiya, Mukaddam, Kanjaksha, Ghosh, Shrimati, Shetty   +3 more
openaire   +2 more sources

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

The dilemma of inherited dysfibrinogenemia during pregnancy

Blood Coagulation & Fibrinolysis, 2012
Inherited dysfibrinogenemia is a rare disorder caused by mutations in the fibrinogen gene, described in approximately 400 families to date. We present the case of a 20-year-old woman at 7 weeks of pregnancy with a history of two first-trimester spontaneous abortions and a family history of thrombotic events.
Javier, Munoz, Jessica, Schering, Angela, Lambing, Salena, Neal, Gregory, Goyert, Pooja M, Green, Amr, Hanbali, Sundara, Raman, Philip, Kuriakose   +8 more
openaire   +2 more sources

Congenital Dysfibrinogenemias

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

Dysfibrinogenemia and placental abruption

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

[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

Congenital (hypo-)dysfibrinogenemia and bleeding: A systematic literature review

Thrombosis Research, 2022
Qiulan Ding
exaly  

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

Clinica Chimica Acta, 2022
Faquan Lin, Liqun Xiang, Meiling Luo
exaly  

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