Haghpanah S - Search Results

1

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: haghpanah s. Blood Coagul Fibrinolysis. 2009 Dec;20(8):642-5. doi: 10.1097/MBC.0b013e32832f4371. Blood Coagul Fibrinolysis. 2009. PMID: 19710607

2

Causes of chronic renal failure among Iranian hemodialysis patients.

Malekmakan L, Haghpanah S, Pakfetrat M, Malekmakan A, Khajehdehi P. Malekmakan L, et al. Among authors: haghpanah s. Saudi J Kidney Dis Transpl. 2009 May;20(3):501-4. Saudi J Kidney Dis Transpl. 2009. PMID: 19414964

3

Malignancies in patients with beta-thalassemia major and beta-thalassemia intermedia: a multicenter study in Iran.

Karimi M, Giti R, Haghpanah S, Azarkeivan A, Hoofar H, Eslami M. Karimi M, et al. Among authors: haghpanah s. Pediatr Blood Cancer. 2009 Dec;53(6):1064-7. doi: 10.1002/pbc.22144. Pediatr Blood Cancer. 2009. PMID: 19533641

4

Effect of combination therapy of hydroxyurea with l-carnitine and magnesium chloride on hematologic parameters and cardiac function of patients with beta-thalassemia intermedia.

Karimi M, Mohammadi F, Behmanesh F, Samani SM, Borzouee M, Amoozgar H, Haghpanah S. Karimi M, et al. Among authors: haghpanah s. Eur J Haematol. 2010 Jan 1;84(1):52-8. doi: 10.1111/j.1600-0609.2009.01356.x. Epub 2009 Oct 3. Eur J Haematol. 2010. PMID: 19799627 Clinical Trial.

5

Adverse effects of hydroxyurea in beta-thalassemia intermedia patients: 10 years' experience.

Karimi M, Cohan N, Mousavizadeh K, Falahi MJ, Haghpanah S. Karimi M, et al. Among authors: haghpanah s. Pediatr Hematol Oncol. 2010 Apr;27(3):205-11. doi: 10.3109/08880011003639952. Pediatr Hematol Oncol. 2010. PMID: 20367264

6

Use of Glubran 2 and Glubran tissue skin adhesive in patients with hereditary bleeding disorders undergoing circumcision and dental extraction.

Haghpanah S, Vafafar A, Golzadeh MH, Ardeshiri R, Karimi M. Haghpanah S, et al. Ann Hematol. 2011 Apr;90(4):463-8. doi: 10.1007/s00277-010-1086-y. Epub 2010 Sep 28. Ann Hematol. 2011. PMID: 20878157

7

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: haghpanah s. Blood Coagul Fibrinolysis. 2011 Jun;22(4):325-30. doi: 10.1097/MBC.0b013e3283457e99. Blood Coagul Fibrinolysis. 2011. PMID: 21415708

8

Serum lipid profiles in patients with beta-thalassemia major and intermedia in southern Iran.

Haghpanah S, Davani M, Samadi B, Ashrafi A, Karimi M. Haghpanah S, et al. J Res Med Sci. 2010 May;15(3):150-4. J Res Med Sci. 2010. PMID: 21526074 Free PMC article.

9

Genotype-phenotype relationship of patients with β-thalassemia taking hydroxyurea: a 13-year experience in Iran.

Karimi M, Haghpanah S, Farhadi A, Yavarian M. Karimi M, et al. Among authors: haghpanah s. Int J Hematol. 2012 Jan;95(1):51-6. doi: 10.1007/s12185-011-0985-6. Epub 2011 Dec 20. Int J Hematol. 2012. PMID: 22180324

10

Cerebral thrombosis in patients with β-thalassemia: a systematic review.

Haghpanah S, Karimi M. Haghpanah S, et al. Blood Coagul Fibrinolysis. 2012 Apr;23(3):212-7. doi: 10.1097/MBC.0b013e3283502975. Blood Coagul Fibrinolysis. 2012. PMID: 22322139 Review.

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