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Volumn 86, Issue 9, 2008, Pages 842-843

Primary adenocarcinoma of the duodenal bulb;Déficit combiné en facteur V et VIII de la coagulation

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 8; FIBRINOGEN; PROTHROMBIN;

EID: 67549093508     PISSN: 00414131     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (2)

References (12)
  • 1
    • 19444368098 scopus 로고
    • Congenital factor V deficiency (parahemophilia) with true hemophilia in two brothers
    • Oeri J, Matter M, Isenschmid H, Hauser F, Koller F. Congenital factor V deficiency (parahemophilia) with true hemophilia in two brothers, Bibl Paediatr 1954;58:575-88.
    • (1954) Bibl Paediatr , vol.58 , pp. 575-588
    • Oeri, J.1    Matter, M.2    Isenschmid, H.3    Hauser, F.4    Koller, F.5
  • 2
    • 0031881892 scopus 로고    scopus 로고
    • Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII
    • Peyvandi F, Tuddenham EGD, Akhtari AM, Lak M, Mannucci PM. Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII, Br J Haematol 1998;100:773-6.
    • (1998) Br J Haematol , vol.100 , pp. 773-776
    • Peyvandi, F.1    Tuddenham, E.G.D.2    Akhtari, A.M.3    Lak, M.4    Mannucci, P.M.5
  • 3
    • 0034981641 scopus 로고    scopus 로고
    • Molecular characterization of the ERGIC-53 gene in two Japanese patients with combined factor V - factor VIII deficiency
    • Dansako H, Ishimaru F, Takai Y, Tomoda J, Nakase K, Fujii K, et al. Molecular characterization of the ERGIC-53 gene in two Japanese patients with combined factor V - factor VIII deficiency, Ann Hematol 2001; 80:292-4.
    • (2001) Ann Hematol , vol.80 , pp. 292-294
    • Dansako, H.1    Ishimaru, F.2    Takai, Y.3    Tomoda, J.4    Nakase, K.5    Fujii, K.6
  • 5
    • 1642369785 scopus 로고    scopus 로고
    • Review of clinical, biochemical and genetic aspects of combined factor V and factor VIII deficiency, and report of a new affected family
    • Elena M. Faionia, Gessica Fontanaa, Giovanni Carpanib, Enza D'Auriac, Giuseppe Banderalic, Gianalessandro Moronib, Marco Cattaneoa. Review of clinical, biochemical and genetic aspects of combined factor V and factor VIII deficiency, and report of a new affected family, Thrombosis research 2005;112: 269-271.
    • (2005) Thrombosis Research , vol.112 , pp. 269-271
    • Faionia, E.M.1    Fontanaa, G.2    Carpanib, G.3    D'Auriac, E.4    Banderalic, G.5    Moronib, G.6    Cattaneoa, M.7
  • 7
    • 0033120795 scopus 로고    scopus 로고
    • ERGIC-53 gene structure and mutation analysis in 19 combined factors Vand VIII deficiency families
    • Nichols WC, Terry VH, Wheatley MA, Yang A, Zivelin A, Ciavarella N et al. ERGIC-53 gene structure and mutation analysis in 19 combined factors Vand VIII deficiency families, Blood 1999;93:2261-6.
    • (1999) Blood , vol.93 , pp. 2261-2266
    • Nichols, W.C.1    Terry, V.H.2    Wheatley, M.A.3    Yang, A.4    Zivelin, A.5    Ciavarella, N.6
  • 8
    • 33847651714 scopus 로고    scopus 로고
    • Combined deficiency of factors V and VIII: When the genetic approach explains combined deficiency in coagulation C
    • Vinciguerraa,b, B. Durandb, L. Rugeria. Combined deficiency of factors V and VIII: when the genetic approach explains combined deficiency in coagulation C, Immuno-analyse et biologie spécialisée 2007;22: 41-42
    • (2007) Immuno-analyse et Biologie Spécialisée , vol.22 , pp. 41-42
    • Vinciguerraa, B.1    Durandb, B.2    Rugeria, L.3
  • 9
    • 0020322169 scopus 로고
    • Combined factor V and factor VIII deficiency among non-Ashkenazi Jews
    • Seligsohn U, Zivelin A, Zwang E. Combined factor V and factor VIII deficiency among non-Ashkenazi Jews, N Engl J Med 1982; 307:11915.
    • (1982) N Engl J Med , vol.307 , pp. 11915
    • Seligsohn, U.1    Zivelin, A.2    Zwang, E.3
  • 11
    • 33847654079 scopus 로고    scopus 로고
    • A mutation in LMAN1 (ERGIC-53) causing combined factors V and VIII deficiency is prevalent in Jews originating from the island of Djerba in Tunisia
    • Segal A, Zivelin A, Rosenberg N, Ginsburg D, Shpilberg O,Seligsohn U. A mutation in LMAN1 (ERGIC-53) causing combined factors V and VIII deficiency is prevalent in Jews originating from the island of Djerba in Tunisia, Blood Coagul Fibrinolysis 2004;15:99102.
    • (2004) Blood Coagul Fibrinolysis , vol.15 , pp. 99102
    • Segal, A.1    Zivelin, A.2    Rosenberg, N.3    Ginsburg, D.4    Shpilberg, O.5    Seligsohn, U.6
  • 12
    • 0031881892 scopus 로고    scopus 로고
    • Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII
    • Peyvandi F, Tuddenham EG, Akhtari AM, Lak M, Mannucci PM. Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII, Br J Haematol 1998;100:7736.
    • (1998) Br J Haematol , vol.100 , pp. 7736
    • Peyvandi, F.1    Tuddenham, E.G.2    Akhtari, A.M.3    Lak, M.4    Mannucci, P.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.