Afrasiabi A - Search Results

1

Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease in southern Iran.

Shamsakhzari S, Afrasiabi A, Haghpanah S, Karimi M. Shamsakhzari S, et al. Among authors: afrasiabi a. Blood Coagul Fibrinolysis. 2011 Jun;22(4):325-30. doi: 10.1097/MBC.0b013e3283457e99. Blood Coagul Fibrinolysis. 2011. PMID: 21415708

2

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. Karimi M, et al. Among authors: afrasiabi a. Blood Coagul Fibrinolysis. 2009 Dec;20(8):642-5. doi: 10.1097/MBC.0b013e32832f4371. Blood Coagul Fibrinolysis. 2009. PMID: 19710607

3

Bleeding symptoms in heterozygous carriers of inherited coagulation disorders in southern Iran.

Mahmoodi M, Peyvandi F, Afrasiabi A, Ghaffarpasand F, Karimi M. Mahmoodi M, et al. Among authors: afrasiabi a. Blood Coagul Fibrinolysis. 2011 Jul;22(5):396-401. doi: 10.1097/MBC.0b013e328345f566. Blood Coagul Fibrinolysis. 2011. PMID: 21451397

4

Genotype-phenotype correlation related to lipid profile in beta-thalassemia major and intermedia in southern Iran.

Bordbar M, Haghpanah S, Afrasiabi A, Dehbozorgian J, Karimi M. Bordbar M, et al. Among authors: afrasiabi a. J Clin Lipidol. 2012 Mar-Apr;6(2):108-13. doi: 10.1016/j.jacl.2011.12.005. Epub 2011 Dec 26. J Clin Lipidol. 2012. PMID: 22385543

5

Comparison of thrombin generation assay with conventional coagulation tests in evaluation of bleeding risk in patients with rare bleeding disorders.

Zekavat OR, Haghpanah S, Dehghani J, Afrasiabi A, Peyvandi F, Karimi M. Zekavat OR, et al. Among authors: afrasiabi a. Clin Appl Thromb Hemost. 2014 Sep;20(6):637-44. doi: 10.1177/1076029613475473. Epub 2013 Feb 6. Clin Appl Thromb Hemost. 2014. PMID: 23393288 Free article. Clinical Trial.

6

Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran.

Karimi M, Cairo A, Safarpour MM, Haghpanah S, Ekramzadeh M, Afrasiabi A, Shahriari M, Menegatti M. Karimi M, et al. Among authors: afrasiabi a. Blood Coagul Fibrinolysis. 2014 Jun;25(4):360-3. doi: 10.1097/MBC.0000000000000046. Blood Coagul Fibrinolysis. 2014. PMID: 24389588

7

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

Karimi M, Vafafar A, Haghpanah S, Payandeh M, Eshghi P, Hoofar H, Afrasiabi A, Gerdabi J, Ardeshiri R, Menegatti M, Peyvandi F. Karimi M, et al. Among authors: afrasiabi a. Haemophilia. 2012 Mar;18(2):211-5. doi: 10.1111/j.1365-2516.2011.02635.x. Epub 2011 Aug 19. Haemophilia. 2012. PMID: 21854511

8

Polymorphisms associated with sickle cell disease in Southern Iran.

Haghpanah S, Nasirabadi S, Kianmehr M, Afrasiabi A, Karimi M. Haghpanah S, et al. Among authors: afrasiabi a. Genetika. 2012 Jul;48(7):890-3. Genetika. 2012. PMID: 22988776

9

Evaluation of Thrombin Generation Assay in Patients With Hemophilia.

Haghpanah S, Bazrafshan A, Silavizadeh S, Dehghani J, Afrasiabi A, Karimi M. Haghpanah S, et al. Among authors: afrasiabi a. Clin Appl Thromb Hemost. 2016 May;22(4):322-6. doi: 10.1177/1076029614555903. Epub 2014 Oct 28. Clin Appl Thromb Hemost. 2016. PMID: 25354749 Free article.

10

Epidemiologic study of patients with thrombotic events referred to a tertiary hospital in Southern Iran.

Akbari A, Haghpanah S, Barzegar H, Shahsavani A, Afrasiabi A, Parand S, Karimi M. Akbari A, et al. Among authors: afrasiabi a. Heliyon. 2021 Aug 8;7(8):e07734. doi: 10.1016/j.heliyon.2021.e07734. eCollection 2021 Aug. Heliyon. 2021. PMID: 34409192 Free PMC article.

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