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Factor XIII deficiency
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editors
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Karimi M, Bereczky Z, Cohan N, Muszbek L editors. Factor XIII deficiency. Seminars in thrombosis and hemostasis. 2009; 35(4):426–38.
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Seminars in Thrombosis and Hemostasis
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Karimi, M.1
Bereczky, Z.2
Cohan, N.3
Muszbek, L.4
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2
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84919949905
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Current understanding in diagnosis and management of factor XIII deficiency
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Naderi M, Dorgalaleh A, Tabibian Sh, Alizadeh Sh, Eshghi P, Solaimani G. Current understanding in diagnosis and management of factor XIII deficiency. Iran J Pediatr Hematol Oncol. 2013;3(4):164–72
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(2013)
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Naderi, M.1
Dorgalaleh, A.2
Tabibian, S.3
Alizadeh, S.4
Eshghi, P.5
Solaimani, G.6
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3
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84919903019
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Factor XIII deficiency in Sistan and Baluchistan province
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Naderi M, Imani M, Eshghi P, Dorgalaleh A, Tabibian S, Alizadeh S. Factor XIII deficiency in Sistan and Baluchistan province. Sci J Blood Transfus Organ. 2013;10(3):282–8.
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Sci J Blood Transfus Organ
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Naderi, M.1
Imani, M.2
Eshghi, P.3
Dorgalaleh, A.4
Tabibian, S.5
Alizadeh, S.6
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4
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84874109899
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Safety of human blood products in rare bleeding disorders in southeast of Iran
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Naderi M, Eshghi P, Saneei Moghaddam E, Alizadeh Sh, Dorgalaleh A. Safety of human blood products in rare bleeding disorders in southeast of Iran. Haemophilia 2013;19:e90–2.
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Haemophilia
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Naderi, M.1
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Dorgalaleh, A.5
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Factor XIII deficiency
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Haemophilia
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Hsieh, L.1
Nugent, D.2
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7
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Central nervous system bleeding in patients with rare bleeding disorders
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Siboni S, Zanon E, Sottilotta G, Consonni D, Castaman G, Mikovic D, et al. Central nervous system bleeding in patients with rare bleeding disorders. Haemophilia 2012;18(1):34–8.
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Long-term prophylaxis in patients with factor XIII deficiency complicated by intracranial haemorrhage in Iran
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Eshghi P, Mahjour S, Naderi M, Dehbozorgian J, Karimi M. Long-term prophylaxis in patients with factor XIII deficiency complicated by intracranial haemorrhage in Iran. Haemophilia 2010;16(2):383–5.
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Haemophilia
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Evaluation of low PAI-1 activity as a risk factor for hemorrhagic diathesis
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Ågren A, Wiman B, Stiller V, Lindmarker P, Sten-Linder M, Carlsson A, et al. Evaluation of low PAI-1 activity as a risk factor for hemorrhagic diathesis. J Thromb Haemost. 2006;4(1):201–8.
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Ågren, A.1
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Plasminogen activator inhibitor type 1 deficiency
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Mehta, R.1
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Polymorphisms of coagulation factor XIII subunit A and risk of nonfatal hemorrhagic stroke in young white women
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Reiner AP, Schwartz SM, Frank MB, Longstreth W, Hindorff LA, Teramura G, et al. Polymorphisms of coagulation factor XIII subunit A and risk of nonfatal hemorrhagic stroke in young white women. Stroke 2001;32(11):2580–7.
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Reiner, A.P.1
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Teramura, G.6
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Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency
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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.
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(2014)
Haemophilia
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Naderi, M.1
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Kazemi, A.6
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Molecular analysis of sixteen unrelated factor XIIIA deficient families from south-east of Iran
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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.
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Molecular basis of inherited factor XIII-A deficiency among patients from Sistan-Baluchestan
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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.
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Eshghi P, Abolghasemi H, Sanei-Moghaddam E, Anwar R, Jazebi M, Amid A, et al. Factor XIII deficiency in south-east Iran. Haemophilia 2004;10(5):470–2.
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Corifact/Fibrogammin(R) P in the prophylactic treatment of hereditary factor XIII deficiency: Results of a prospective, multicenter, open-label study
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Epub 2013/03/06
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Nugent D. Corifact/Fibrogammin(R) P in the prophylactic treatment of hereditary factor XIII deficiency: results of a prospective, multicenter, open-label study. Thromb Res. 2012; 130(Suppl 2):S12–4. Epub 2013/03/06.
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Nugent, D.1
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Intracranial hemorrhage pattern in the patients with factor XIII deficiency
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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. 2013:1–5.
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18
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The 4G/4G genotype at nucleotide position -675 in the promoter region of the plasminogen activator inhibitor 1 (PAI-1) gene is less frequent in young patients with minor stroke than controls
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Endler G, Lalouschek W, Exner M, Mitterbauer G, Haring D, Mannhalter C. The 4G/4G genotype at nucleotide position -675 in the promoter region of the plasminogen activator inhibitor 1 (PAI-1) gene is less frequent in young patients with minor stroke than controls. Br J Haematol. 2000;110: 469–71.
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Plasminogen activator inhibitor 4G polymorphism is associated with decreased risk of cerebrovascular mortality in older women
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Roest M, van der Schouw YT, Banga JD, Tempelman MJ, de Groot PG, Sixma JJ, et al. Plasminogen activator inhibitor 4G polymorphism is associated with decreased risk of cerebrovascular mortality in older women. Circulation 2000;101:67–70.
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