Cerebral thrombosis in patients with β-thalassemia: a systematic reviewHAGHPANAH, Sezaneh; KARIMI, Mehran.Blood coagulation & fibrinolysis. 2012, Vol 23, Num 3, pp 212-217, issn 0957-5235, 6 p.Article

Diagnosis and Management of von Willebrand Disease in IranCOHAN, Nader; KARIMI, Mehran.Seminars in thrombosis and hemostasis. 2011, Vol 37, Num 5, pp 602-606, issn 0094-6176, 5 p.Article

Genotype―phenotype relationship of patients with β-thalassemia taking hydroxyurea: a 13-year experience in IranKARIMI, Mehran; HAGHPANAH, Sezaneh; FARHADI, Ali et al.International journal of hematology. 2012, Vol 95, Num 1, pp 51-56, issn 0925-5710, 6 p.Article

Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease in southern IranSHAMSAKHZARI, Shoeleh; AFRASIABI, Abdolreza; HAGHPANAH, Sezaneh et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 4, pp 325-330, issn 0957-5235, 6 p.Article

Magnetic resonance imaging to determine the incidence of brain ischaemia in patients with β-thalassaemia intermediaKARIMI, Mehran; BAGHERI, Hadi; RASTGU, Fatemeh et al.Thrombosis and haemostasis. 2010, Vol 103, Num 5, pp 989-993, issn 0340-6245, 5 p.Article

Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiencyKARIMI, Mehran; MENEGATTI, Marzia; AFRASIABI, Abdolreza et al.Haematologica (Roma). 2008, Vol 93, Num 6, pp 934-938, issn 0390-6078, 5 p.Article

Clinical response of patients with sickle cell anemia to cromolyn sodium nasal sprayKARIMI, Mehran; ZEKAVAT, Omid R; SHARIFZADEH, Sedigeh et al.American journal of hematology. 2006, Vol 81, Num 11, pp 809-816, issn 0361-8609, 8 p.Article

A rare inherited coagulation disorder: Combined homozygous factor VII and factor X deficiencyMENEGATTI, Marzia; KARIMI, Mehran; GARAGIOLA, Isabella et al.American journal of hematology. 2004, Vol 77, Num 1, pp 90-91, issn 0361-8609, 2 p.Article

Bleeding symptoms in heterozygous carriers of inherited coagulation disorders in southern IranMAHMOODI, Mojtaba; PEYVANDI, Flora; AFRASIABI, Abdolreza et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 5, pp 396-401, issn 0957-5235, 6 p.Article

Factor XIII DeficiencyKARIMI, Mehran; BERECZKY, Zsuzsanna; COHAN, Nader et al.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 426-438, issn 0094-6176, 13 p.Article

Cost-utility analysis of oral deferasirox versus infusional deferoxamine in transfusion-dependent β-thalassemia patientsKESHTKARAN, Ali; JAVANBAKHT, Mehdi; SALAVATI, Sedigheh et al.Transfusion (Philadelphia, PA). 2013, Vol 53, Num 8, pp 1722-1729, issn 0041-1132, 8 p.Article

Topiramate and Propranolol for Prophylaxis of MigraineFALLAH, Razieh; MOHAMMAD SALEH DIVANIZADEH; KARIMI, Mehran et al.Indian journal of pediatrics. 2013, Vol 80, Num 11, pp 920-924, issn 0019-5456, 5 p.Article

Response to hydroxyurea treatment in Iranian transfusion-dependent β-thalassemia patientsYAVARIAN, Majid; KARIMI, Mehran; BAKKER, Egbert et al.Haematologica (Roma). 2004, Vol 89, Num 10, pp 1172-1178, issn 0390-6078, 7 p.Article

Patients with localized and disseminated tumors have reduced but measurable levels of ADAMTS-13 (von Willebrand factor cleaving protease)MANNUCCIO MANNUCCI, Pier; KARIMI, Mehran; MOSALAEI, Ahmad et al.Haematologica (Roma). 2003, Vol 88, Num 4, pp 454-458, issn 0390-6078, 5 p.Article

Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratoryKARIMI, Mehran; HAGHPANAH, Sezaneh; AMIRHAKIMI, Anis et al.Blood coagulation & fibrinolysis. 2009, Vol 20, Num 8, pp 642-645, issn 0957-5235, 4 p.Article

A lump on the headKARIMI, Mehran; COHAN, Nader; MOHAMAD HADI BAGHERI et al.Lancet (British edition). 2008, Vol 372, Num 9647, pp 1436-1436, issn 0140-6736, 1 p.Article

Replacement therapy for bleeding episodes in factor VII deficiency A prospective evaluationMARIANI, Guglielmo; NAPOLITANO, Mariasanta; SCHVED, Jean F et al.Thrombosis and haemostasis. 2013, Vol 109, Num 2, pp 238-247, issn 0340-6245, 10 p.Article

Cytology of leukemic lymphadenopathyKUMAR, Perikala V; KARIMI, Mehran; MONABATI, Ahmad et al.Acta cytologica. 2002, Vol 46, Num 5, pp 801-807, issn 0001-5547Article

Contemporary approaches to treatment of beta-thalassemia intermediaTAHER, Ali T; MUSALLAM, Khaled M; KARIMI, Mehran et al.Blood reviews. 2012, Vol 26, issn 0268-960X, S24-S27, SUP1Article

Age-related complications in treatment-naïve patients with thalassaemia intermediaTAHER, Ali T; MUSALLAM, Khaled M; EL-BESHLAWY, Amal et al.British journal of haematology. 2010, Vol 150, Num 4, pp 486-489, issn 0007-1048, 4 p.Article

Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE studyTAHER, Ali T; MUSALLAM, Khaled M; KARIMI, Mehran et al.Blood. 2010, Vol 115, Num 10, pp 1886-1892, issn 0006-4971, 7 p.Article

The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpuraPALLA, Roberta; LAVORETANO, Silvia; LOMBARDI, Rossana et al.Haematologica (Roma). 2009, Vol 94, Num 2, pp 289-293, issn 0390-6078, 5 p.Article

Mutational screening of six afibrinogenemic patients : Identification and characterization of four novel molecular defectsMONALDINI, Luca; ASSELTA, Rosanna; DUGA, Stefano et al.Thrombosis and haemostasis. 2007, Vol 97, Num 4, pp 546-551, issn 0340-6245, 6 p.Article

Subclassification of localized Leishmania lymphadenitis in fine needle aspiration smearsKUMAR, Perikala V; MOOSAVI, Abdollah; KARIMI, Mehran et al.Acta cytologica. 2001, Vol 45, Num 4, pp 547-554, issn 0001-5547Article