Volume 12 (2024)
Volume 11 (2023)
Volume 10 (2022)
Volume 9 (2021)
Volume 8 (2020)
Volume 7 (2019)
Volume 6 (2018)
Volume 5 (2017)
Volume 4 (2016)
Volume 3 (2015)
Volume 2 (2014)
Volume 1 (2013)
Immunomodulation of TLR2 and TLR4 by G2013 (alfa-L-Guluronic acid) in CVID Patients
Immunomodulation of TLR2 and TLR4 by G2013 (alfa-L-Guluronic acid) in CVID Patients

Laleh Sharifi; Asghar Aghamohammadi; Monireh Mohsenzadegan; Nima Rezaei; Farzaneh Towfighi Zavareh; Mona Moshiri; Saied Bokaie; Anis Barati; Seyed Javad Sayedi; Gholamreza Azizi; Abbas Mirshafiey

Volume 5, Issue 7 , July 2017, , Pages 5327-5337

https://doi.org/10.22038/ijp.2017.23562.1985

Abstract
  Background: Common variable immunodeficiency (CVID) is a primary immune disorder associated with hypogammaglobulinemia, recurrent infections and autoimmune diseases. CVID patients are ...  Read More
Academic Performance, Sleep Disorders and Their Association in Middle School Students in Iran
Academic Performance, Sleep Disorders and Their Association in Middle School Students in Iran

Mohsen Reisi; Rozita Jalilian; Gholamreza Azizi; Afsane Rashti; Jamal Faghihi nia; Mojtaba Akbari; Nazanin Babaei; Seyed Javad Sayedi; Nima Rezaei; Mohammad Reza Modaresi

Volume 5, Issue 3 , March 2017, , Pages 4541-4549

https://doi.org/10.22038/ijp.2017.21374.1794

Abstract
  Background: Although sleep disorders are common problems among families and they affect the learning, memory processes and academic performance of children, there is no evaluation of ...  Read More
Phospho-SMC1 in-Cell ELISA based Detection of Ataxia Telangiectasia
Phospho-SMC1 in-Cell ELISA based Detection of Ataxia Telangiectasia

Majid Zaki dizaji; Nima Rezaei; Marjan Yaghmaie; Mehdi Yaseri; Seyed Javad Sayedi; Gholamreza Azizi; Asghar Aghamohammadi; Seyed Mohammad Akrami

Volume 4, Issue 12 , December 2016, , Pages 3957-3967

https://doi.org/10.22038/ijp.2016.7751

Abstract
  BackgroundAtaxia telangiectasia (A-T) is a common genetically inherited cause of early childhood-onset ataxia. The infrequency of this disease, vast phenotype variation, disorders with ...  Read More