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Volumn 54, Issue 4, 2008, Pages 765-768

Evaluation of a prolonged prothrombin time

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 7;

EID: 42449142326     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1373/clinchem.2007.100818     Document Type: Article
Times cited : (26)

References (9)
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    • How to interpret and pursue an abnormal prothrombin time, activated partial thromboplastin time, and bleeding time in adults
    • Kamal AH, Tefferi A, Pruthi RK. How to interpret and pursue an abnormal prothrombin time, activated partial thromboplastin time, and bleeding time in adults. Mayo Clin Proc 2007;82:864-73.
    • (2007) Mayo Clin Proc , vol.82 , pp. 864-873
    • Kamal, A.H.1    Tefferi, A.2    Pruthi, R.K.3
  • 2
    • 2942585598 scopus 로고    scopus 로고
    • Acquired isolated factor VII deficiency associated with severe bleeding and successful treatment with recombinant FVIIa (NovoSeven)
    • Mullighan CG, Rischbieth A, Duncan EM, Lloyd JV. Acquired isolated factor VII deficiency associated with severe bleeding and successful treatment with recombinant FVIIa (NovoSeven). Blood Coag Fibrinol 2004;15:347-51.
    • (2004) Blood Coag Fibrinol , vol.15 , pp. 347-351
    • Mullighan, C.G.1    Rischbieth, A.2    Duncan, E.M.3    Lloyd, J.V.4
  • 3
    • 27844481104 scopus 로고    scopus 로고
    • Potential predictors of bleeding risk in inherited factor VII deficiency: Clinical, biological and molecular criteria
    • Giansily-Blaizot M, Schved J-F. Potential predictors of bleeding risk in inherited factor VII deficiency: clinical, biological and molecular criteria. Thromb Haemostasis 2005;94:901-6.
    • (2005) Thromb Haemostasis , vol.94 , pp. 901-906
    • Giansily-Blaizot, M.1    Schved, J.-F.2
  • 5
    • 0018192517 scopus 로고
    • Factor VII Padua: A congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern
    • Girolami A, Fabris F, Dal Bo Zanon R, Ghiotto G, Burul A. Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern. J Lab Clin Med 1978;91:387-95.
    • (1978) J Lab Clin Med , vol.91 , pp. 387-395
    • Girolami, A.1    Fabris, F.2    Dal3    Bo Zanon, R.4    Ghiotto, G.5    Burul, A.6
  • 6
    • 0025871447 scopus 로고
    • Purification and characterization of factor VII 304-Gln: A variant molecule with reduced activity isolated from a clinically unaffected male
    • O'Brien DP, Gale KM, Anderson JS, McVey JH, Miller GJ, Meade TW, Tuddenham EGD. Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected male. Blood 1991;78(1):132-40.
    • (1991) Blood , vol.78 , Issue.1 , pp. 132-140
    • O'Brien, D.P.1    Gale, K.M.2    Anderson, J.S.3    McVey, J.H.4    Miller, G.J.5    Meade, T.W.6    Tuddenham, E.G.D.7
  • 7
    • 33646013915 scopus 로고    scopus 로고
    • Congenital factor VII deficiency: Therapy with recombinant activated factor VII-a critical appraisal
    • Mariani G, Konkle BA, Ingerslev J. Congenital factor VII deficiency: therapy with recombinant activated factor VII-a critical appraisal. Haemophilia 2006; 12:19-27.
    • (2006) Haemophilia , vol.12 , pp. 19-27
    • Mariani, G.1    Konkle, B.A.2    Ingerslev, J.3
  • 8
    • 33846839272 scopus 로고    scopus 로고
    • Use of recombinant factor VIIa for hip surgery in a patient with factor-VII deficiency: A case report
    • Gopalan PK, Clohisy JC, Cashen AF, Eby CS. Use of recombinant factor VIIa for hip surgery in a patient with factor-VII deficiency: a case report. J Bone Joint Surg Am 2007;89A(2):389-91.
    • (2007) J Bone Joint Surg Am , vol.89 A , Issue.2 , pp. 389-391
    • Gopalan, P.K.1    Clohisy, J.C.2    Cashen, A.F.3    Eby, C.S.4
  • 9
    • 4844229372 scopus 로고    scopus 로고
    • The rare coagulation disorders-review with guidelines for management from the United Kingdom Haemophila Center Doctors' Organization
    • Bolton-Maggs PHB, Perry DJ, Chalmers EA, Parapia LA, Wilde JT, Williams MD, et al. The rare coagulation disorders-review with guidelines for management from the United Kingdom Haemophila Center Doctors' Organization. Haemophilia 2004;10:593-628.
    • (2004) Haemophilia , vol.10 , pp. 593-628
    • Bolton-Maggs, P.H.B.1    Perry, D.J.2    Chalmers, E.A.3    Parapia, L.A.4    Wilde, J.T.5    Williams, M.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.