| Quality of life among Iranian patients with beta-thalassemia major using the SF-36 questionnaire S Haghpanah, S Nasirabadi, F Ghaffarpasand, R Karami, M Mahmoodi, ... Sao Paulo medical journal 131, 166-172, 2013 | 81 | 2013 |
| Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory M Karimi, S Haghpanah, A Amirhakimi, AR Afrasiabi, J Dehbozorgian, ... Blood coagulation & fibrinolysis 20 (8), 642-645, 2009 | 36 | 2009 |
| Bruck syndrome—a rare syndrome of bone fragility and joint contracture and novel homozygous FKBP10 mutation H Moravej, H Karamifar, Z Karamizadeh, G Amirhakimi, S Atashi, ... Endokrynologia Polska 66 (2), 170-174, 2015 | 31 | 2015 |
| Juvenile Paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation F Saki, Z Karamizadeh, S Nasirabadi, S Mumm, WH McAlister, MP Whyte Journal of Bone and Mineral Research 28 (6), 1501-1508, 2013 | 29 | 2013 |
| Sociocultural challenges of beta-thalassaemia major birth in carriers of beta-thalassaemia in Iran S Haghpanah, S Nasirabadi, N Rahimi, H Faramarzi, M Karimi Journal of medical screening 19 (3), 109-111, 2012 | 22 | 2012 |
| The impact of renin–angiotensin system, angiotensin І converting enzyme (insertion/deletion), and angiotensin ІІ type 1 receptor (A1166C) polymorphisms on breast cancer … S Namazi, A Daneshian, M Mohammadianpanah, P Jafari, ... Gene 532 (1), 108-114, 2013 | 13 | 2013 |
| Coagulation disorders in women with idiopathic menorrhagia M Karimi, A Afrasiabi, S Amoei, J Zolghadri, S Nasirabadi, M Bordbar, ... Asia Pacific J Oncol Hematol 2, 111-4, 2010 | 5 | 2010 |
| Polymorphisms associated with sickle cell disease in Southern Iran S Haghpanah, S Nasirabadi, M Kianmehr, A Afrasiabi, M Karimi Russian Journal of Genetics 48, 755-757, 2012 | 3 | 2012 |
| Combined α-thalassemia and Hemoglobin J-Iran (β77 His→ Asp). A Family Study in southern Iran SJ Dehghani, AA Dashtarzhen, S Nasirabadi, J Dehbozorgian, ... Iranian Red Crescent Medical Journal 13 (8), 586, 2011 | 2 | 2011 |
| A Classic Case of Maple Syrup Urine Disease and a Novel Mutation in the BCKDHA Gene A Mirzaee, N Pishva, Z Karamizadeh, J Kohlhase, S Purarian, F Hemmati, ... Iranian Journal of Neonatology 8 (3), 72-74, 2017 | 1 | 2017 |
| Relationship of the Interaction Between Two Quantitative Trait Loci with γ-Globin Expression in β-Thalassemia Intermedia Patients S NickAria, S Haghpanah, M Ramzi, M Karimi Hemoglobin 42 (2), 108-112, 2018 | | 2018 |
| Phenotypic Bleeding Penetrance in Female Carriers of Rare Inherited Coagulation Deficiency M Karimi, S Nasirabadi, M Mahmoodi, R Ardeshiri HAEMOPHILIA 18, 205-205, 2012 | | 2012 |
| Survey of coagulation disorders in women with idiopathic menorhagia M Karimi, A Afrasiabi, S Amoei, S Nasirabadi, J Zolghadri HAEMOPHILIA 14, 156-156, 2008 | | 2008 |
| Carrier detection and prenatal diagnosis in high risk families M Karimi, A Afrasiabi, F Peyvandi, M Margalione, I Garagiola, ... HAEMOPHILIA 14, 6-6, 2008 | | 2008 |
