Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fibrinogens, Abnormal/genetics"'
Autor:
Christine Biron-Andréani, Lionel Reyftmann, Richard J. Fish, Philippe de Moerloose, Chandrasekaran Nagaswami, Pierre Boulot, John W. Weisel, Silja Vorjohann, Marguerite Neerman-Arbez
Publikováno v:
Thrombosis and Haemostasis, Vol. 104, No 5 (2010) pp. 990-997
SummaryInherited disorders of fibrinogen are rare and affect either the quantity (hypofibrinogenaemia and afibrinogenaemia) or the quality of the circulating fibrinogen (dysfibrinogenaemia) or both (hypodysfibrinogenaemia). Extensive allelic heteroge
Autor:
Philippe de Moerloose, Joanna Basa, Marguerite Neerman-Arbez, Joanna Zdziarska, Anetta Undas, Aleksander B. Skotnicki, Teresa Iwaniec
Publikováno v:
Blood Coagulation and Fibrinolysis, Vol. 20, No 5 (2009) pp. 374-6
We report a case of hypofibrinogenemia caused by heterozygosity for gamma Ala82Gly in a 69-year-old Polish woman with severe bleeding tendency and a history of six miscarriages. She suffered from frequent mucocutaneous bleedings, epistaxes requiring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c95cca5d079fcf6e1c2f9f2983664a9e
https://archive-ouverte.unige.ch/unige:5480
https://archive-ouverte.unige.ch/unige:5480
Autor:
Marguerite Neerman-Arbez, Helia Robert-Ebadi, Agnès Le Querrec, Sylvie Gandon-Laloum, Annie Borel Derlon, Philippe de Moerloose
Publikováno v:
Blood Coagulation and Fibrinolysis, Vol. 19, No 7 (2008) pp. 697-9
A 5-year-old boy was hospitalized for acute appendicitis. Routine preoperative hemostasis screening resulted in a diagnosis of dysfibrinogenemia. Fifteen days after the operation the patient was re-hospitalized for deep vein thrombosis. Genetic analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d37f98cc0f4cb97e4417d47f6b7220c
https://archive-ouverte.unige.ch/unige:1432
https://archive-ouverte.unige.ch/unige:1432