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)
Apolipoprotein E serum levels in children with Guillain-Barre Syndrome in northwest of Iran
Apolipoprotein E serum levels in children with Guillain-Barre Syndrome in northwest of Iran

Lida Saboktakin; Mohammad Barzegar; Ahad Ghazavi

Volume 10, Issue 9 , September 2022, , Pages 16673-16682

https://doi.org/10.22038/ijp.2022.65207.4923

Abstract
  Background: Guillain-Barre syndrome (GBS) is an acute immune-mediated disease that affects both adults and children. Many infectious and non-infectious conditions may trigger this disease. ...  Read More
Epidemiology and Outcomes of Arterial Ischemic Stroke in Children Admitted to Tabriz Children’s Hospital, Tabriz, Iran during (2014-2019)
Epidemiology and Outcomes of Arterial Ischemic Stroke in Children Admitted to Tabriz Children’s Hospital, Tabriz, Iran during (2014-2019)

Shadi Shiva; Mohammad Barzegar; Monireh Rashidzadeh

Volume 9, Issue 7 , July 2021, , Pages 13887-13894

https://doi.org/10.22038/ijp.2021.56747.4458

Abstract
  BackgroundArterial ischemic stroke (AIS) is an important cause of neurological disabilities, such as hemiparesis, epilepsy, and cognitive dysfunction in children. This study aimed to ...  Read More
A Patient with Tuberous Sclerosis Complex and Spinal Muscular Atrophy; A Case Report
A Patient with Tuberous Sclerosis Complex and Spinal Muscular Atrophy; A Case Report

Sina Raeisi; Hassan Bakhtiary; Mohammad Barzegar

Volume 8, Issue 8 , August 2020, , Pages 11855-11860

https://doi.org/10.22038/ijp.2020.49604.3967

Abstract
  Background Tuberous Sclerosis Complex (TSC), and Spinal Muscular Atrophy (SMA) are two inherited disorders while they are genetically independent. TSC is characterized by the formation ...  Read More
Tay-Sachs Disease in Two Iranian Identical Male Twins; A Case Report
Tay-Sachs Disease in Two Iranian Identical Male Twins; A Case Report

Bita Poorshiri; Mohammad Barzegar; Sina Raeisi; Mohammadreza Afghan

Volume 8, Issue 5 , May 2020, , Pages 11355-11359

https://doi.org/10.22038/ijp.2020.45083.3710

Abstract
  Background Tay-Sachs disease is an autosomal-recessive lysosomal storage metabolic disorder. The typical symptoms of the disease include ataxia, muscle weakness, and mental disorders. ...  Read More