Hosseini S - Search Results

1

Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency.

Dorgalaleh A, Zaker F, Tabibian S, Alizadeh S, Dorgalele S, Hosseini S, Shamsizadeh M. Dorgalaleh A, et al. Among authors: hosseini s. Blood Coagul Fibrinolysis. 2016 Apr;27(3):324-7. doi: 10.1097/MBC.0000000000000435. Blood Coagul Fibrinolysis. 2016. PMID: 26891460 Review.

2

Detection and biological characteristic of FLT3 gene mutations in children with acute leukemia.

Nasiri N, Shaikhy M, Zaker F, Hosseini S, Moosavi SA, Marjani AJ. Nasiri N, et al. Among authors: hosseini s. Arch Iran Med. 2014 Apr;17(4):258-61. Arch Iran Med. 2014. PMID: 24724602

3

Congenital combined deficiency of coagulation factors: a study of seven patients.

Naderi M, Tabibian S, Hosseini MS, Alizadeh S, Hosseini S, Shamsizadeh M, Dorgalaleh A. Naderi M, et al. Among authors: hosseini s, hosseini ms. Blood Coagul Fibrinolysis. 2015 Jan;26(1):59-62. doi: 10.1097/MBC.0000000000000180. Blood Coagul Fibrinolysis. 2015. PMID: 25215615

4

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

Naderi M, Dorgalaleh A, Alizadeh S, Tabibian S, Hosseini S, Shamsizadeh M, Bamedi T. Naderi M, et al. Among authors: hosseini s. Int J Hematol. 2014 Nov;100(5):443-9. doi: 10.1007/s12185-014-1664-1. Epub 2014 Sep 18. Int J Hematol. 2014. PMID: 25230816

5

Congenital factor V deficiency: comparison of the severity of clinical presentations among patients with rare bleeding disorders.

Naderi M, Tabibian S, Alizadeh S, Hosseini S, Zaker F, Bamedi T, Shamsizadeh M, Dorgalaleh A. Naderi M, et al. Among authors: hosseini s. Acta Haematol. 2015;133(2):148-54. doi: 10.1159/000363598. Epub 2014 Sep 26. Acta Haematol. 2015. PMID: 25277779 Clinical Trial.

6

Factor XIII deficiency in Iran: a comprehensive review of the literature.

Dorgalaleh A, Naderi M, Hosseini MS, Alizadeh S, Hosseini S, Tabibian S, Eshghi P. Dorgalaleh A, et al. Among authors: hosseini s, hosseini ms. Semin Thromb Hemost. 2015 Apr;41(3):323-9. doi: 10.1055/s-0034-1395350. Epub 2015 Jan 23. Semin Thromb Hemost. 2015. PMID: 25615432 Review.

7

Inhibition of factor XIIa, a new approach in management of thrombosis.

Dorgalaleh A, Hosseini MS, Mobaraki RN, Alizadeh S, Hosseini S, Tabibian S, Shamsizadeh M, Moghaddam ES, Khosravi S, Rahimizadeh A. Dorgalaleh A, et al. Among authors: hosseini s, hosseini ms. Ann Transl Med. 2015 May;3(Suppl 1):S20. doi: 10.3978/j.issn.2305-5839.2015.02.14. Ann Transl Med. 2015. PMID: 26046066 Free PMC article. No abstract available.

8

Challenges in implementation of ISTH diagnostic algorithm for diagnosis and classification of factor XIII deficiency in Iran.

Dorgalaleh A, Farshi Y, Alizadeh SH, Naderi M, Tabibian SH, Kazemi A, Hosseini S. Dorgalaleh A, et al. Among authors: hosseini s. J Thromb Haemost. 2015 Sep;13(9):1735-6. doi: 10.1111/jth.13037. Epub 2015 Jul 15. J Thromb Haemost. 2015. PMID: 26099358 Free article. No abstract available.

9

Effect of Social Factors on the Highest Global Incidence of Congenital Factor XIII Deficiency in Southeast of Iran.

Naderi M, Alizadeh S, Tabibian S, Hosseini S, Varmaghani B, Shamsizadeh M, Dorgalaleh A. Naderi M, et al. Among authors: hosseini s. Arch Iran Med. 2015 May;18(5):331. Arch Iran Med. 2015. PMID: 26155604 No abstract available.

10

First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran.

Hosseini S, Dorgalaleh A, Bamedi T, Tavakol K, Tabibian S, Naderi M, Alizadeh S, Varmaghani B, Shamsizadeh M, Rahimizadeh A, Ebrahimi S. Hosseini S, et al. Blood Coagul Fibrinolysis. 2015 Dec;26(8):908-11. doi: 10.1097/MBC.0000000000000358. Blood Coagul Fibrinolysis. 2015. PMID: 26226252

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