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Volumn 6, Issue SUPPL. 2, 2008, Pages

National and international registries of rare bleeding disorders

Author keywords

Database; Rare Bleeding Disorders; RBDs; Registry

Indexed keywords

BLOOD CLOTTING FACTOR; BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 13; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; VITAMIN K GROUP;

EID: 56649091112     PISSN: 17232007     EISSN: None     Source Type: Journal    
DOI: 10.2450/2008.0037-08     Document Type: Conference Paper
Times cited : (41)

References (13)
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  • 3
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  • 4
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  • 5
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    • Acharya SS, Coughlin A, Dimichele DM; North American Rare Bleeding Disorder Study Group. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004; 2: 248-56.
    • Acharya SS, Coughlin A, Dimichele DM; North American Rare Bleeding Disorder Study Group. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004; 2: 248-56.
  • 6
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    • Tahani A, Kudsi M. National registry of congenital bleeding disorders in Syria. World Federation of Haemophilia, Istanbul, 2-5 June 2008-06-12.
    • Tahani A, Kudsi M. National registry of congenital bleeding disorders in Syria. World Federation of Haemophilia, Istanbul, 2-5 June 2008-06-12.
  • 7
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    • Ivaskevicius V, Seitz R, Kohler HP, et al. Establishment of an international registry of patients with inherited FXIII deficiency. World Federation of Haemophiha, Istanbul, 2-5 June 2008-06-12.
    • Ivaskevicius V, Seitz R, Kohler HP, et al. Establishment of an international registry of patients with inherited FXIII deficiency. World Federation of Haemophiha, Istanbul, 2-5 June 2008-06-12.
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    • The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation
    • Bolton-Maggs PH, Perry DJ, Chalmers EA, et al. The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia 2004; 10: 593-628.
    • (2004) Haemophilia , vol.10 , pp. 593-628
    • Bolton-Maggs, P.H.1    Perry, D.J.2    Chalmers, E.A.3
  • 10
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    • Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII
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  • 11
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    • Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex
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  • 12
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  • 13
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    • Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
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    • Rost, S.1    Fregin, A.2    Ivaskevicius, V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.