메뉴 건너뛰기




Volumn 18, Issue 2, 2012, Pages 211-215

Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran

Author keywords

Efficacy; Factor X deficiency; Genotype; Iran; Prophylaxis

Indexed keywords

BLOOD CLOTTING FACTOR; BLOOD CLOTTING FACTOR 10; RECOMBINANT BLOOD CLOTTING FACTOR 10; UNCLASSIFIED DRUG;

EID: 84857113202     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2011.02635.x     Document Type: Article
Times cited : (34)

References (15)
  • 1
    • 33646032774 scopus 로고    scopus 로고
    • Prophylaxis in rare coagulation disorders - factor X deficiency
    • Auerswald G. Prophylaxis in rare coagulation disorders - factor X deficiency. Thromb Res 2006; 118(Suppl 1): S29-31.
    • (2006) Thromb Res , vol.118 , Issue.SUPPL. 1
    • Auerswald, G.1
  • 2
    • 33747168208 scopus 로고    scopus 로고
    • Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene
    • Herrmann FH, Auerswald G, Ruiz-Saez A et al. Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene. Haemophilia 2006; 12: 479-89.
    • (2006) Haemophilia , vol.12 , pp. 479-489
    • Herrmann, F.H.1    Auerswald, G.2    Ruiz-Saez, A.3
  • 3
    • 34248512983 scopus 로고    scopus 로고
    • Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment
    • Ingerslev J, Herlin T, Sorensen B, Clausen N, Chu KC, High KA. Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment. Haemophilia 2007; 13: 334-6.
    • (2007) Haemophilia , vol.13 , pp. 334-336
    • Ingerslev, J.1    Herlin, T.2    Sorensen, B.3    Clausen, N.4    Chu, K.C.5    High, K.A.6
  • 4
    • 18844480017 scopus 로고    scopus 로고
    • Molecular analysis of the genotype-phenotype relationship in factor X deficiency
    • Millar DS, Elliston L, Deex P et al. Molecular analysis of the genotype-phenotype relationship in factor X deficiency. Hum Genet 2000; 106: 249-57.
    • (2000) Hum Genet , vol.106 , pp. 249-257
    • Millar, D.S.1    Elliston, L.2    Deex, P.3
  • 5
    • 0031848372 scopus 로고    scopus 로고
    • Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients
    • Peyvandi F, Mannucci PM, Lak M et al. Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients. Br J Haematol 1998; 102: 626-8.
    • (1998) Br J Haematol , vol.102 , pp. 626-628
    • Peyvandi, F.1    Mannucci, P.M.2    Lak, M.3
  • 6
    • 70449578675 scopus 로고    scopus 로고
    • Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory
    • Karimi M, Haghpanah S, Amirhakimi A, Afrasiabi A, Dehbozorgian J, Nasirabady S. Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory. Blood Coagul Fibrinolysis 2009; 20: 642-5.
    • (2009) Blood Coagul Fibrinolysis , vol.20 , pp. 642-645
    • Karimi, M.1    Haghpanah, S.2    Amirhakimi, A.3    Afrasiabi, A.4    Dehbozorgian, J.5    Nasirabady, S.6
  • 7
    • 32644452195 scopus 로고    scopus 로고
    • Hereditary coagulation factor X deficiency
    • Kumar A, Mishra KL, Mishra D. Hereditary coagulation factor X deficiency. Indian Pediatr 2005; 42: 1240-2.
    • (2005) Indian Pediatr , vol.42 , pp. 1240-1242
    • Kumar, A.1    Mishra, K.L.2    Mishra, D.3
  • 8
    • 44949140390 scopus 로고    scopus 로고
    • Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency
    • Karimi M, Menegatti M, Afrasiabi A, Sarikhani S, Peyvandi F. Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency. Haematologica 2008; 93: 934-8.
    • (2008) Haematologica , vol.93 , pp. 934-938
    • Karimi, M.1    Menegatti, M.2    Afrasiabi, A.3    Sarikhani, S.4    Peyvandi, F.5
  • 9
    • 0022638498 scopus 로고
    • Severe congenital factor X deficiency with intracranial haemorrhage
    • Sumer T, Ahmad M, Sumer NK, Al-Mouzan MI. Severe congenital factor X deficiency with intracranial haemorrhage. Eur J Pediatr 1986; 145: 119-20.
    • (1986) Eur J Pediatr , vol.145 , pp. 119-120
    • Sumer, T.1    Ahmad, M.2    Sumer, N.K.3    Al-Mouzan, M.I.4
  • 10
    • 11844272623 scopus 로고    scopus 로고
    • Homozygous Factor X gene mutations Gly380Arg and Tyr163delAT are associated with perinatal intracranial hemorrhage
    • Herrmann FH, Navarette M, Salazar-Sanchez L, Carillo JM, Auerswald G, Wulff K. Homozygous Factor X gene mutations Gly380Arg and Tyr163delAT are associated with perinatal intracranial hemorrhage. J Pediatr 2005; 146: 128-30.
    • (2005) J Pediatr , vol.146 , pp. 128-130
    • Herrmann, F.H.1    Navarette, M.2    Salazar-Sanchez, L.3    Carillo, J.M.4    Auerswald, G.5    Wulff, K.6
  • 11
    • 0036862292 scopus 로고    scopus 로고
    • Inherited coagulation disorders in southern Iran
    • Karimi M, Yarmohammadi H, Ardeshiri R. Inherited coagulation disorders in southern Iran. Haemophilia 2002; 8: 740-4.
    • (2002) Haemophilia , vol.8 , pp. 740-744
    • Karimi, M.1    Yarmohammadi, H.2    Ardeshiri, R.3
  • 12
    • 0036104076 scopus 로고    scopus 로고
    • Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency
    • Peyvandi F, Menegatti M, Santagostino E et al. Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency. Br J Haematol 2002; 117: 685-92.
    • (2002) Br J Haematol , vol.117 , pp. 685-692
    • Peyvandi, F.1    Menegatti, M.2    Santagostino, E.3
  • 13
    • 0035077839 scopus 로고    scopus 로고
    • Prophylactic treatment of severe factor X deficiency with prothrombin complex concentrate
    • Kouides PA, Kulzer L. Prophylactic treatment of severe factor X deficiency with prothrombin complex concentrate. Haemophilia 2001; 7: 220-3.
    • (2001) Haemophilia , vol.7 , pp. 220-223
    • Kouides, P.A.1    Kulzer, L.2
  • 14
    • 0033918212 scopus 로고    scopus 로고
    • Quantification of D-dimer using a new fully automated assay: its application for the diagnosis of deep vein thrombosis
    • Villa P, Ferrando F, Serra J et al. Quantification of D-dimer using a new fully automated assay: its application for the diagnosis of deep vein thrombosis. Haematologica 2000; 85: 520.
    • (2000) Haematologica , vol.85 , pp. 520
    • Villa, P.1    Ferrando, F.2    Serra, J.3
  • 15
    • 0344131428 scopus 로고    scopus 로고
    • Thrombogenicity of prothrombin complex concentrates
    • Kohler M. Thrombogenicity of prothrombin complex concentrates. Thromb Res 1999; 95: S13-7.
    • (1999) Thromb Res , vol.95
    • Kohler, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.