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Volumn 8, Issue 7, 1997, Pages 441-444

Fibrinogen poissy I: A new case of the Aα Arg 16His fibrinogen variant

Author keywords

Disseminated intravascular coagulation; Dysfibrinogen; Fibrinogen; Mutation

Indexed keywords

ARGININE; BATROXOBIN; DNA; FIBRIN; FIBRIN DEGRADATION PRODUCT; FIBRINOGEN; FIBRINOPEPTIDE; HISTIDINE; MUTANT PROTEIN; THROMBIN;

EID: 0030657589     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001721-199710000-00010     Document Type: Article
Times cited : (5)

References (12)
  • 1
    • 0028877613 scopus 로고
    • Familial dysfibrinogenemia and thrombophilia. Report on a study of the SCC subcomittee on fibrinogen
    • Haverkate F, Samama M. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SCC subcomittee on fibrinogen. Thromb Haemost 1995; 73: 151-161.
    • (1995) Thromb Haemost , vol.73 , pp. 151-161
    • Haverkate, F.1    Samama, M.2
  • 3
    • 0002146137 scopus 로고
    • Dysfibrinogenemia and other disorders of fibrinogen structure and function
    • Colman RW, Hirsh J, Marder VJ Salzman EW, eds. Philadelphia: Lippincott Company
    • McDonagh J, Carrell N, Lee MH. Dysfibrinogenemia and other disorders of fibrinogen structure and function. In: Colman RW, Hirsh J, Marder VJ Salzman EW, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. Philadelphia: Lippincott Company, 1994; 314-334.
    • (1994) Hemostasis and Thrombosis: Basic Principles and Clinical Practice , pp. 314-334
    • McDonagh, J.1    Carrell, N.2    Lee, M.H.3
  • 5
    • 0015122124 scopus 로고
    • Fibrinogen Bethesda: A congenital dysfibrinogenemia with delayed fibrinopeptide release
    • Gralnick HR, Givelber HM, Shainoff JR, Finlayson JS. Fibrinogen Bethesda: a congenital dysfibrinogenemia with delayed fibrinopeptide release. J Clin Invest 1971; 50: 1819-1830.
    • (1971) J Clin Invest , vol.50 , pp. 1819-1830
    • Gralnick, H.R.1    Givelber, H.M.2    Shainoff, J.R.3    Finlayson, J.S.4
  • 7
    • 0028314865 scopus 로고
    • Mutation in blood coagulation factor V associated with resistance to activated protein C
    • Bertina RM, Koeleman PC, Koster T, Rosendaal FR, Dirven RJ, Ronde H, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369: 64-67.
    • (1994) Nature , vol.369 , pp. 64-67
    • Bertina, R.M.1    Koeleman, P.C.2    Koster, T.3    Rosendaal, F.R.4    Dirven, R.J.5    Ronde, H.6
  • 8
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
    • Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-3703.
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 9
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylene-tetrahydrofolate reductase
    • Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylene-tetrahydrofolate reductase. Nature Genet 1995; 10: 111-113.
    • (1995) Nature Genet , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3    Goyette, P.4    Sheppard, C.A.5    Matthews, R.G.6
  • 10
    • 0023941028 scopus 로고
    • Fibrinogen Birmingham: A heterozygous dysfibrinogenemia (AαArg His) containing heterodimeric molecules
    • Siebenlist KR, Prchal JT, Mosesson MW. Fibrinogen Birmingham: a heterozygous dysfibrinogenemia (AαArg His) containing heterodimeric molecules. Blood 1988; 71: 613-618.
    • (1988) Blood , vol.71 , pp. 613-618
    • Siebenlist, K.R.1    Prchal, J.T.2    Mosesson, M.W.3
  • 11
    • 0027724649 scopus 로고
    • Inherited dysfibrinogenemia: Emerging abnormal structure associations with pathologic and nonpathologic dysfunctions
    • Galanakis DK. Inherited dysfibrinogenemia: emerging abnormal structure associations with pathologic and nonpathologic dysfunctions. Sem Thromb Hemost 1993; 19: 386-395.
    • (1993) Sem Thromb Hemost , vol.19 , pp. 386-395
    • Galanakis, D.K.1
  • 12
    • 0008411076 scopus 로고    scopus 로고
    • Hereditary dysfibrinogenemia, afibrinogenemia, hypofibrinogenemia and thrombosis
    • Seghatchian MJ, Samama MM, Hecker SP, eds. Boca Raton, New York, London, Tokyo: CRC Press
    • Samama MM, Haverkate F. Hereditary dysfibrinogenemia, afibrinogenemia, hypofibrinogenemia and thrombosis. In: Seghatchian MJ, Samama MM, Hecker SP, eds. Hypercoagulable states. Fundamental Aspects, Acquired Disorders, and Congenital Thrombophilia. Boca Raton, New York, London, Tokyo: CRC Press, 1996; 379-384.
    • (1996) Hypercoagulable States. Fundamental Aspects, Acquired Disorders, and Congenital Thrombophilia , pp. 379-384
    • Samama, M.M.1    Haverkate, F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.