| Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency M Naderi, A Dorgalaleh, S Alizadeh, S Tabibian, S Hosseini, ... International journal of hematology 100, 443-449, 2014 | 89 | 2014 |
| Factor XIII deficiency in Iran: a comprehensive review of the literature A Dorgalaleh, M Naderi, MS Hosseini, S Alizadeh, S Hosseini, S Tabibian, ... Seminars in thrombosis and hemostasis 41 (03), 323-329, 2015 | 88 | 2015 |
| Guidelines for laboratory diagnosis of factor XIII deficiency A Dorgalaleh, S Tabibian, S Hosseini, M Shamsizadeh Blood coagulation & fibrinolysis 27 (4), 361-364, 2016 | 54 | 2016 |
| Congenital factor V deficiency: comparison of the severity of clinical presentations among patients with rare bleeding disorders M Naderi, S Tabibian, S Alizadeh, S Hosseini, F Zaker, T Bamedi, ... Acta haematologica 133 (2), 148-154, 2015 | 38 | 2015 |
| No correlation between interleukin-10 gene promoter polymorphisms and hepatitis B virus infection outcome M Sofian, E Kalantar, A Aghakhani, S Hosseini, M Banifazl, A Eslamifar, ... Hepatitis monthly 13 (5), 2013 | 36 | 2013 |
| Genetic risk factors in patients with deep venous thrombosis, a retrospective case control study on Iranian population S Hosseini, E Kalantar, MS Hosseini, S Tabibian, M Shamsizadeh, ... Thrombosis journal 13, 1-6, 2015 | 34 | 2015 |
| Challenges in implementation of ISTH diagnostic algorithm for diagnosis and classification of factor XIII deficiency in Iran AK A. Dorgalaleh,S.Hosseini journal of thrombosis and hemostasis 13 (9), 1735-1736, 2015 | 25* | 2015 |
| Rare bleeding disorders: a narrative review of epidemiology, molecular and clinical presentations, diagnosis and treatment M Naderi, S Tabibian, MS Hosseini, S Alizadeh, S Hosseini, H Karami, ... Journal of Pediatrics Review 2 (2), 31-46, 2014 | 17 | 2014 |
| Congenital combined deficiency of coagulation factors: a study of seven patients M Naderi, S Tabibian, MS Hosseini, S Alizadeh, S Hosseini, ... Blood Coagulation & Fibrinolysis 26 (1), 59-62, 2015 | 16 | 2015 |
| EFFECT OF SOCIAL FACTORS ON THE HIGHEST GLOBAL INCIDENCE OF CONGENITAL FACTOR XIII DEFICIENCY IN SOUTHEAST OF IRAN M Naderi, S Alizadeh, S Tabibian, S Hosseini, B VARMAGHANI, ... ARCHIVES OF IRANIAN MEDICINE 18 (5), 331-331, 2015 | 15 | 2015 |
| Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency A Dorgalaleh, F Zaker, S Tabibian, S Alizadeh, S Dorgalele, S Hosseini, ... Blood coagulation & fibrinolysis 27 (3), 324-327, 2016 | 13 | 2016 |
| A Fetal Hemolytic Anemia in a Child with Cytomegalovirus Infection S Hosseini, E Kalantar iranian Journal of Pediatric Hematology Oncology 4 (2), 78-83, 2014 | 10 | 2014 |
| Lack of association between interleukin-10 gene promoter polymorphisms with HIV susceptibility and progression to AIDS A Ramezani, E Kalantar, A Aghakhani, M Banifazl, M Foroughi, ... Iranian journal of pathology 10 (2), 141, 2015 | 9 | 2015 |
| Evaluation of complement regulatory components in patients with atypical hemolytic uremic syndrome H Soudabeh, K Ebrahim, H Nakisa, D Akbar, HS Rozita, T Bamedi Central European Journal of Immunology 39 (1), 67-70, 2014 | 8 | 2014 |
| First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran S Hosseini, A Dorgalaleh, T Bamedi, K Tavakol, S Tabibian, M Naderi, ... Blood Coagulation & Fibrinolysis 26 (8), 908-911, 2015 | 7 | 2015 |
| A Novel Homozygous MYO7A Mutation: Case Report EK Mahsa Ahmadi , Ali Dehghanifard , Soudabeh Hosseini Acta Medica Iranica, , No. 5 (2018) 56 (5), 348-350, 2018 | 5* | 2018 |
| The Prevalence and Incidence of Atypical Hemolytic Uremic Syndrome in Iran; A Systematic Review and Meta-Analysis Protocol Study N Hooman, M Sadeghian, F Jahangiri, S Hosseini Journal of Comprehensive Pediatrics, 2017 | 5 | 2017 |
| Bilateral maxillary, sphenoid sinuses and lumbosacral spinal cord extramedullary relapse of CML following allogeneic stem cell transplant S Hosseini, S Ansari, P Vosough, G Bahoush, AA Hamidieh, ... International Journal of Hematology-Oncology and Stem Cell Research 10 (2), 106, 2016 | 5 | 2016 |
| A Long Term Screening of Iranian Populations with Thalassemia and Hemoglobinopathies S Hosseini, E Kalantar, A Dorgalaleh British biomedical bulletin, 2014 | 5 | 2014 |
| Detection and biological characteristic of FLT3 gene mutations in children with acute leukemia HS Nasiri Nahid,Zaker farhad Archives of Iranian medicine 17 (4), 258, 2014 | 4 | 2014 |
shaban alizadehHematology department, Allied medical school, Tehran University of Medical Sciences, Tehran,IranVerified email at sina.tums.ac.ir
