| Factor XIII deficiency M Karimi, Z Bereczky, N Cohan, L Muszbek Seminars in thrombosis and hemostasis 35 (04), 426-438, 2009 | 258 | 2009 |
| Changes in platelet count and mean platelet volume during infectious and inflammatory disease and their correlation with ESR and CRP S Zareifar, MR Farahmand Far, F Golfeshan, N Cohan Journal of clinical laboratory analysis 28 (3), 245-248, 2014 | 126 | 2014 |
| Guidelines for diagnosis and management of Beta-thalassemia intermedia M Karimi, N Cohan, V De Sanctis, NS Mallat, A Taher Pediatric hematology and oncology 31 (7), 583-596, 2014 | 107 | 2014 |
| Cancer-associated thrombosis M Karimi, N Cohan The open cardiovascular medicine journal 4, 78, 2010 | 101 | 2010 |
| Anemia and iron deficiency in adolescent school girls in kavar urban area, southern iran M Ramzi, S Haghpanah, L Malekmakan, N Cohan, A Baseri, A Alamdari, ... Iranian Red Crescent Medical Journal 13 (2), 128, 2011 | 97 | 2011 |
| Association between iron status and febrile seizures in children S Zareifar, HR Hosseinzadeh, N Cohan Seizure 21 (8), 603-605, 2012 | 67 | 2012 |
| Echocardiographic finding in beta‐thalassemia intermedia and major: absence of pulmonary hypertension following hydroxyurea treatment in beta‐thalassemia intermedia M Karimi, M Borzouee, A Mehrabani, N Cohan European journal of haematology 82 (3), 213-218, 2009 | 54 | 2009 |
| Adverse effects of hydroxyurea in β-thalassemia intermedia patients: 10 years’ experience M Karimi, N Cohan, K Moosavizadeh, M Javad Falahi, S Haghpanah Pediatric hematology and oncology 27 (3), 205-211, 2010 | 46 | 2010 |
| Prevalence and prognostic impact of Wilms' tumor 1 (WT1) gene, including SNP rs16754 in cytogenetically normal acute myeloblastic leukemia (CN-AML): An Iranian experience G Toogeh, M Ramzi, M Faranoush, N Amirizadeh, S Haghpanah, ... Clinical Lymphoma Myeloma and Leukemia 16 (3), e21-e26, 2016 | 39 | 2016 |
| Hydroxyurea as a first-line treatment of extramedullary hematopoiesis in patients with beta thalassemia: Four case reports M Karimi, N Cohan, P Pishdad Hematology 20 (1), 53-57, 2015 | 34 | 2015 |
| Successful delivery in patients with FXIII deficiency receiving prophylaxis: report of 17 cases in Iran M Naderi, P Eshghi, N Cohan, E Miri‐Moghaddam, M Yaghmaee, ... Haemophilia 18 (5), 773-776, 2012 | 30 | 2012 |
| The efficacy of a neonatal screening programme in decreasing the hospitalization rate of patients with G6PD deficiency in southern Iran N Cohan, M Karimi, AH Khalili, MH Falahzadeh, B Samadi, RM Mahdavi Journal of medical screening 17 (2), 66-67, 2010 | 28 | 2010 |
| Evaluation of health related quality of life in 6–18 years old patients with acute leukemia during chemotherapy S Zareifar, MR Farahmandfar, N Cohan, F Modarresnia, S Haghpanah The Indian Journal of Pediatrics 79, 177-182, 2012 | 25 | 2012 |
| Attitude toward prenatal diagnosis for β-thalassemia major and medical abortion in Southern Iran M Karimi, S Johari, N Cohan Hemoglobin 34 (1), 49-54, 2010 | 24 | 2010 |
| Reduction of thrombus size in murine models of thrombosis following administration of recombinant α1-proteinase inhibitor mutant proteins WP Sheffield, LJ Eltringham-Smith, V Bhakta, S Gataiance Thrombosis and haemostasis 107 (05), 972-984, 2012 | 21 | 2012 |
| Factor XIII deficiency: a review of literature P Eshghi, N Cohan, M Naderi, M Karimi IJBC 4 (2), 85-91, 2012 | 21 | 2012 |
| Efficacy of combined desferrioxamine and deferiprone versus single desferrioxamine therapy in patients with major thalassemia S ZAREEIFAR, AAH JABARI, N KOHAN, S Haghpanah ARCHIVES OF IRANIAN MEDICINE 12 (5), 488-491, 2009 | 21 | 2009 |
| Comparison of the umbilical artery blood gas, nucleated red blood cell, C-reactive protein, and white blood cell differential counts between neonates of diabetic and … BN Jahromi, N Ahmadi, N Cohan, MRN Jahromi Taiwanese Journal of Obstetrics and Gynecology 50 (3), 301-305, 2011 | 20 | 2011 |
| Initial presentation of acute lymphoblastic leukemia with osteoporosis and multiple spontaneous bone fractures N Cohan, S Sarikhani, S Moslemi, M Karimi Iranian Red Crescent Medical Journal 13 (1), 52, 2011 | 19 | 2011 |
| Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran P Eshghi, N Cohan, M Lak, M Naderi, F Peyvandi, M Menegatti, M Karimi Clinical and Applied Thrombosis/Hemostasis 18 (1), 100-103, 2012 | 18 | 2012 |
sezaneh haghpanahProfessor of Community Medicine, Hematology Research Center, Shiraz University of Medical SciencesVerified email at sums.ac.ir
