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Mohammad Mostafa Safarpour
Mohammad Mostafa Safarpour
Verified email at sums.ac.ir
Title
Cited by
Cited by
Year
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
202014
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
152020
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
52021
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
52018
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
52017
Candida albicans endophthalmitis following penetrating keratoplasty: A case report
S Bamdad, A Meshksar, MM Safarpour
Electronic Physician 10 (1), 6215, 2018
42018
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
22021
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
12023
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
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