Results 91 to 100 of about 1,246 (182)
Detection of the dysfibrinogenemia with molecular genetic analysis in Korean population
, 2004 의학과/박사[한글] 유전성 이상섬유소원혈증은 4번 염색체의 장완(q23-q32)에 위치한 섬유소원 유전자의 결함으로 인해 발생한다. 지금까지 분자유전적 결함이 보고된 부위는 α-사슬 유전자의 엑손 2, 4, 5 번, β-사슬 유전자의 엑손 2, 4 번, γ-사슬 유전자의 엑손 7, 8, 9 번 등이다.
박노진
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Fibrinogen Sevilla, a congenital dysfibrinogenemia characterized by an abnormal monomer aggregation and a defective plasmin lysis [PDF]
, 1989 A dysfibrinogenemia (fibrinogen Sevilla) was detected in a 64-yr-old woman with no previous history of hemorrhagic diathesis or thrombosis. Thrombin and reptilase times were prolonged.
Noguerol, P. (P.) +5 more
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, 2013 BACKGROUND: Dysfibrinogenemia is a rare group of qualitative fibrinogen disorders caused by structural abnormalities in the fibrinogen molecule. The laboratory diagnosis of dysfibrinogenemia is controversial.
Ramanathan, Ramshanker +5 more
core +1 more source
“Dysfibrinogenemia Jujuy”, associated to bleeding Disorders
, 2020 El objetivo del presente trabajo fue estudiar a una joven paciente con manifestaciones hemorrágicas, caracterizar su fibrina plasmática e identificar la posible alteración molecular del fibrinógeno de la paciente y sus familiares directos. Se diagnosticó
Lauricella, Ana María +3 more
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, 1991 Headache, papilledema and visual disturbances accompanied by increased intracranial pressure in the absence of an identifiable mass lesion define the diagnosis of pseudotumor cerebri.
Robert F. Lindberg; David I. Kaufman; Houria Hassounia; Philip Lee Shettle
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Stroke in two young siblings with congenital dysfibrinogenemia.
, 1983 Roncaglioni MC +6 more
core +1 more source
A Double Whammy of Mycotic Aneurysms and Acquired Dysfibrinogenemia in a Patient with Septicemia
Balkan Medical Journal, 2021 Chun Yang Sim +3 more
doaj +1 more source