Publications by authors named "Nader Cohan"

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Acute graft-vs-host disease, pathophysiology, prevention, and treatment: Something old and something new.
Nader Cohan, Mani Ramzi, Aren Dermarderosian, Mojtaba Akhtari

J Investig Med· January 2026

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Coagulation Factor VII Deficiency: A Review of the Clinical Implications and Approaches to Replacement Therapy and Prophylaxis.
Nader Cohan, Elham Abedi, Mehran Karimi

Pediatr Blood Cancer· September 2025

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Cytokine Levels in Patients with β-Thalassemia Major and Healthy Individuals: a Systematic Review and Meta-Analysis.
Sezaneh Haghpanah, Mahnaz Hosseini-Bensenjan, Mehrab Sayadi, Farnoosh Nozari, Mani Ramzi, Nader Cohan

Clin Lab· November 2022

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Postpartum Hemorrhage in Heterozygote Factor XIII Deficient Women Compared With Healthy Women. A Cross-Sectional Experience From Iran.
Majid Naderi, Ilia Mirzaei, Saeedeh Yaghoubi, Ida Milani, Nader Cohan

Clin Appl Thromb Hemost· February 2022

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The effect of T helper (Th)/T cytotoxic (Tc) ratio on disease severity in type A hemophilia patients.
Hossein Ali Khazaei, Majid Naderi, Ghasem Miri Aliabad, Seyed Mohammad Nasiraldin Tabatabaei, Ali Alidadi, Nader Cohan

Hum Antibodies· September 2021

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Effects of three months of treatment with vitamin E and N-acetyl cysteine on the oxidative balance in patients with transfusion-dependent β-thalassemia.
Sezaneh Haghpanah, Nader Cohan, Mohammadreza Bordbar, Asghar Bazrafshan, Mehran Karimi

Ann Hematol· March 2021

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Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia.
Omid Reza Zekavat, Mahshid Zareian Jahromi, Sezaneh Haghpanah, Zahra Kargar Jahromi, Nader Cohan

J Pediatr Hematol Oncol· January 2021

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Hb S (: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients.
Azita Azarkeivan, Nader Cohan, Hamid Reza Niazkar, Arsalan Azizi, Fariba Rad

Hemoglobin· March 2020

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Inhibitors against rFVIIa in patients with severe congenital FVII deficiency: A case series.
Peyman Eshghi, S Zahra Tara, Mohammad Reza Baghaipour, Mohammed Reza Bordbar, Alireza Jenabzade, Nader Cohan

Haemophilia· September 2019

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Correlation of bleeding score with frequency and severity of bleeding symptoms in FXIII deficiency assessing by the ISTH Bleeding Assessment Tool.
Majid Naderi, Nader Cohan, Sezaneh Haghpanah, Ghasem Miri-Aliabad, Iraj Shahramian

Transfus Apher Sci· August 2019

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A retrospective study on clinical manifestations of neonates with FXIII-A deficiency.
Majid Naderi, Nader Cohan, Iraj Shahramian, Ghasem Miri-Aliabad, Sezaneh Haghpanah

Blood Cells Mol Dis· July 2019

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Wilms Tumor-1 (WT1) rs16754 Polymorphism and Clinical Outcome in Acute Myeloid Leukemia.
Mani Ramzi, Mohamad Moghadam, Nader Cohan

Turk J Haematol· February 2019

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The Zinc and Copper Levels in Thalassemia Major Patients, Receiving Iron Chelation Therapy.
Omid R Zekavat, Ayda Bahmanjahromi, Sezaneh Haghpanah, Sara Ebrahimi, Nader Cohan

J Pediatr Hematol Oncol· April 2018

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Efficacy and safety of factor eight inhibitor bypassing activity prophylaxis evaluation in young patients with hemophilia and high titer inhibitor.
Mehran Karimi, Hakimeh Tavoosi, Sezaneh Haghpanah, Resvan Ardeshiri, Zohreh Zahedi, Nader Cohan

Blood Coagul Fibrinolysis· March 2016

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Prevalence and Prognostic Impact of Wilms' Tumor 1 (WT1) Gene, Including SNP rs16754 in Cytogenetically Normal Acute Myeloblastic Leukemia (CN-AML): An Iranian Experience.
Gholamreza Toogeh, Mani Ramzi, Mohammad Faranoush, Naser Amirizadeh, Sezaneh Haghpanah, Nader Cohan

Clin Lymphoma Myeloma Leuk· March 2016

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Hydroxyurea as a first-line treatment of extramedullary hematopoiesis in patients with beta thalassemia: Four case reports.
Mehran Karimi, Nader Cohan, Parisa Pishdad

Hematology· January 2015

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Guidelines for diagnosis and management of Beta-thalassemia intermedia.
Mehran Karimi, Nader Cohan, Vincenzo De Sanctis, Naji S Mallat, Ali Taher

Pediatr Hematol Oncol· October 2014

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Changes in platelet count and mean platelet volume during infectious and inflammatory disease and their correlation with ESR and CRP.
Soheila Zareifar, Mohammad Reza Farahmand Far, Fatemeh Golfeshan, Nader Cohan

J Clin Lab Anal· May 2014

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Prevalence of G6PD Deficiency in Neonatal Sepsis in Iran.
Soheila Zareifar, Narjes Pishva, Mohamadreza Farahmandfar, Shahab Benaei, Nader Cohan

Iran J Pediatr· February 2014

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Management of Bleeding in Post-liver Disease, Surgery and Biopsy in Patients With High Uncorrected International Normalized Ratio With Prothrombin Complex Concentrate: An Iranian Experience.
Alireza Parand, Naser Honar, Khashayar Aflaki, Mohammad Hadi Imanieh, Mahmood Haghighat, Nader Cohan

Iran Red Crescent Med J· December 2013

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The association of glutathione S-transferase gene mutations (including GSTT1 and GSTM1) with the prognostic factors and relapse in acute lymphoblastic leukemia.
Soheila Zareifar, Ahmad Monabati, Amir Saeed, Farzaneh Fakhraee, Nader Cohan

Pediatr Hematol Oncol· September 2013

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The evaluation of cisplatin effect on tubular function in children on chemotherapy.
Soheila Zareifar, Hamed Jafari, Bita Geramizadeh, Mitra Basiratnia, Habibollah Golafshan, Nader Cohan

Pediatr Hematol Oncol· February 2013

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Iranian experience of deferasirox (Exjade(®)) in transfusion-dependent patients with iron overload: what is the most effective dose based on serum ferritin levels?
Mehran Karimi, Azita Azarkeivan, Soheila Zareifar, Nader Cohan, Mohammad Reza Bordbar

Hematology· November 2012

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Association between iron status and febrile seizures in children.
Soheila Zareifar, Hamid Reza Hosseinzadeh, Nader Cohan

Seizure· October 2012

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Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran.
Peyman Eshghi, Nader Cohan, Manigeh Lak, Majid Naderi, Flora Peyvandi

Clin Appl Thromb Hemost· June 2012

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