Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran M Karimi, A Cairo, MM Safarpour, S Haghpanah, M Ekramzadeh, ... Blood coagulation & fibrinolysis 25 (4), 360-363, 2014 | 20 | 2014 |
Evaluation of the effect of topical interferon α2b as a complementary treatment of macular edema of patients with diabetic retinopathy: a double-blind placebo-controlled … M Afarid, A Meshksar, A Salehi, MM Safarpour Retina 40 (5), 936-942, 2020 | 15 | 2020 |
Prognostic role of lymphovascular invasion in patients with early breast cancer M Akrami, A Meshksar, JM Ghoddusi, MM Safarpour, S Tahmasebi, ... Indian Journal of Surgical Oncology 12 (4), 671-677, 2021 | 5 | 2021 |
Modified primary prophylaxis in previously untreated patients with severe hemophilia A in Iran M Karimi, P Eshghi, MM Safarpour, S Haghpanah, A Meshksar, Z Zahedi, ... Journal of Pediatric Hematology/Oncology 40 (3), 188-191, 2018 | 5 | 2018 |
Phenotype report on patients with congenital Factor V deficiency in Southern Iran: recent ten years’ experience MM Safarpour, S Haghpanah, A Meshksar, M Karimi Turkish Journal of Hematology 34 (3), 250, 2017 | 5 | 2017 |
Candida albicans endophthalmitis following penetrating keratoplasty: A case report S Bamdad, A Meshksar, MM Safarpour Electronic Physician 10 (1), 6215, 2018 | 4 | 2018 |
Liver transplant for metastatic neuroendocrine tumors: a single-center report of 15 cases AM Moradi, M Entezari, MM Safarpour, A Meshksar, S Muhammad, ... Exp Clin Transplant 19 (6), 588-591, 2021 | 2 | 2021 |
Primary hydatid cyst of the thyroid glands: two case reports and a review of the literature MM Safarpour, S Aminnia, A Dehghanian, R Borazjani, HR Abbassi, ... Journal of Medical Case Reports 17 (1), 417, 2023 | 1 | 2023 |
Modified primary prophylaxis in previously untreated patients with severe hemophilia A in Iran M Karimi, P Eshghi, A Meshksar, MM Safarpour, S Haghpanah, Z Zahedi, ... HAEMOPHILIA 22, 73-73, 2016 | | 2016 |
Phenotype Report on Patients with Congenital Factor V Deficiency in Southern Iran M Karimi, MM Safarpour, S Haghpanah, A Meshksar HAEMOPHILIA 22, 124-124, 2016 | | 2016 |
Genotype and phenotype report on patients with congenital fibrinogen deficiency in south of Iran M Karimi, MM Safarpour, S Haghpanah, A Meshksar, A Afrasiabi, ... JOURNAL OF THROMBOSIS AND HAEMOSTASIS 13, 438-439, 2015 | | 2015 |
Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran M Karimi, M Safarpour, M Ekramzadeh, A Afrasiabi, S Haghpanah, ... HAEMOPHILIA 18, 185-186, 2012 | | 2012 |
Güney İran’daki Konjenital Faktör V Eksikliği Olan Hastaların Fenotip Özelliklerinin Bildirimi: Son On Yıllık Deneyim MM Safarpour, S Haghpanah, A Meshksar, M Karimi | | |