메뉴 건너뛰기




Volumn 100, Issue 5, 2014, Pages 443-449

Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency

Author keywords

Clinical manifestation; Factor XIII deficiency; Hemorrhagic disorder

Indexed keywords

ARGININE; BLOOD CLOTTING FACTOR 13 CONCENTRATE; BLOOD CLOTTING FACTOR 13A; TRYPSIN; BLOOD CLOTTING FACTOR 13;

EID: 84919916817     PISSN: 09255710     EISSN: 18653774     Source Type: Journal    
DOI: 10.1007/s12185-014-1664-1     Document Type: Article
Times cited : (73)

References (17)
  • 3
    • 55949088269 scopus 로고    scopus 로고
    • Factor XIII deficiency
    • COI: 1:CAS:528:DC%2BD1MXkt1alsg%3D%3D, PID: 19141159
    • Hsieh L, Nugent D. Factor XIII deficiency. Haemophilia. 2008;14(6):1190–200.
    • (2008) Haemophilia , vol.14 , Issue.6 , pp. 1190-1200
    • Hsieh, L.1    Nugent, D.2
  • 4
    • 0036682920 scopus 로고    scopus 로고
    • Role of factor XIII in fibrin clot formation and effects of genetic polymorphisms
    • PID: 12130481
    • Ariëns RA, Lai T-S, Weisel JW, Greenberg CS, Grant PJ. Role of factor XIII in fibrin clot formation and effects of genetic polymorphisms. Blood. 2002;100(3):743–54.
    • (2002) Blood , vol.100 , Issue.3 , pp. 743-754
    • Ariëns, R.A.1    Lai, T.-S.2    Weisel, J.W.3    Greenberg, C.S.4    Grant, P.J.5
  • 7
    • 17144445992 scopus 로고    scopus 로고
    • Delayed umbilical bleeding—a presenting feature for factor XIII deficiency: Clinical features, genetics, and management
    • PID: 11826242
    • Anwar R, Minford A, Gallivan L, Trinh CH, Markham AF. Delayed umbilical bleeding—a presenting feature for factor XIII deficiency: clinical features, genetics, and management. Pediatrics. 2002;109(2):e32.
    • (2002) Pediatrics , vol.109 , Issue.2 , pp. e32
    • Anwar, R.1    Minford, A.2    Gallivan, L.3    Trinh, C.H.4    Markham, A.F.5
  • 8
    • 2142649140 scopus 로고    scopus 로고
    • Ali Sharifian A, Karimi K, Mannucci P. Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency
    • COI: 1:STN:280:DC%2BD3sznslKltg%3D%3D, PID: 12911609
    • Lak M, Peyvandi F. Ali Sharifian A, Karimi K, Mannucci P. Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency. J Thromb Haemost. 2003;1(8):1852–3.
    • (2003) J Thromb Haemost , vol.1 , Issue.8 , pp. 1852-1853
    • Lak, M.1    Peyvandi, F.2
  • 10
    • 80051671241 scopus 로고    scopus 로고
    • An update of the mutation profile of factor 13 A and B genes
    • COI: 1:CAS:528:DC%2BC3MXhtVGmsrbO, PID: 21640452
    • Biswas A, Ivaskevicius V, Seitz R, Thomas A, Oldenburg J. An update of the mutation profile of factor 13 A and B genes. Blood Rev. 2011;25(5):193–204.
    • (2011) Blood Rev , vol.25 , Issue.5 , pp. 193-204
    • Biswas, A.1    Ivaskevicius, V.2    Seitz, R.3    Thomas, A.4    Oldenburg, J.5
  • 11
    • 84857609229 scopus 로고    scopus 로고
    • Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran
    • COI: 1:CAS:528:DC%2BC38Xks1eiuro%3D, PID: 22156982
    • Eshghi P, Cohan N, Lak M, Naderi M, Peyvandi F, Menegatti M, et al. Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran. Clin Appl Thromb Hemost. 2012;18(1):100–3.
    • (2012) Clin Appl Thromb Hemost , vol.18 , Issue.1 , pp. 100-103
    • Eshghi, P.1    Cohan, N.2    Lak, M.3    Naderi, M.4    Peyvandi, F.5    Menegatti, M.6
  • 12
    • 39049106677 scopus 로고    scopus 로고
    • Molecular analysis of sixteen unrelated factor XIIIA deficient families from south-east of Iran
    • COI: 1:CAS:528:DC%2BD1cXkt1ersb8%3D, PID: 18275437
    • Trinh CH, Sh ElSayed W, Eshghi P, Miri-Moghaddam E, Zadeh-Vakili A, Markham AF, et al. Molecular analysis of sixteen unrelated factor XIIIA deficient families from south-east of Iran. Br J Haematol. 2008;140(5):581–4.
    • (2008) Br J Haematol , vol.140 , Issue.5 , pp. 581-584
    • Trinh, C.H.1    Sh ElSayed, W.2    Eshghi, P.3    Miri-Moghaddam, E.4    Zadeh-Vakili, A.5    Markham, A.F.6
  • 14
    • 84890860410 scopus 로고    scopus 로고
    • Molecular basis of inherited factor XIII-A deficiency among patients from Sistan–Baluchestan
    • Tamaddon GH, Kazemi A, Rastegar G, Alla F, Hejazi S. Molecular basis of inherited factor XIII-A deficiency among patients from Sistan–Baluchestan. Zahedan J Res Med Sci. 2010;11(4):19–24.
    • (2010) Zahedan J Res Med Sci , vol.11 , Issue.4 , pp. 19-24
    • Tamaddon, G.H.1    Kazemi, A.2    Rastegar, G.3    Alla, F.4    Hejazi, S.5
  • 15
    • 0036736431 scopus 로고    scopus 로고
    • Unusual presentation of factor XIII deficiency
    • COI: 1:STN:280:DC%2BD38vkt1KmsQ%3D%3D, PID: 12199683
    • Almeida A, Khair K, et al. Unusual presentation of factor XIII deficiency. Haemophilia. 2002;8(5):703–5.
    • (2002) Haemophilia , vol.8 , Issue.5 , pp. 703-705
    • Almeida, A.1    Khair, K.2
  • 16
    • 84890860409 scopus 로고    scopus 로고
    • Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency
    • COI: 1:CAS:528:DC%2BC3sXitVWjsr%2FI, PID: 24354489
    • Naderi M, Dorgalaleh A, Alizadeh S, Kashani Khatib Z, Tabibian S, Kazemi A, et al. Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency. Haemophilia. 2014;20(1):e89–92.
    • (2014) Haemophilia , vol.20 , Issue.1 , pp. e89-e92
    • Naderi, M.1    Dorgalaleh, A.2    Alizadeh, S.3    Kashani Khatib, Z.4    Tabibian, S.5    Kazemi, A.6
  • 17
    • 84896399898 scopus 로고    scopus 로고
    • Intracranial hemorrhage pattern in the patients with factor XIII deficiency
    • COI: 1:CAS:528:DC%2BC3sXhs1KjurjN, PID: 24149912
    • Naderi M, Zarei T, Haghpanah S, Eshghi P, Miri-Moghaddam E, Karimi M. Intracranial hemorrhage pattern in the patients with factor XIII deficiency. Ann Hematol. 2014;93(4):693–7.
    • (2014) Ann Hematol , vol.93 , Issue.4 , pp. 693-697
    • Naderi, M.1    Zarei, T.2    Haghpanah, S.3    Eshghi, P.4    Miri-Moghaddam, E.5    Karimi, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.