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)
Transcobalamin Deficiency with the Mutation of Tcn2 in Children with the Primary Diagnosis of Methylmalonic Academia
Transcobalamin Deficiency with the Mutation of Tcn2 in Children with the Primary Diagnosis of Methylmalonic Academia

Sara Nikpour; Peyman Eshraghi; Ehsan Ghayoor; Nosrat Ghaemi; Sepideh Bagheri; Samaneh Norouziasl; Mojtaba Lotfi

Volume 11, Issue 7 , July 2023, , Pages 18099-18103

https://doi.org/10.22038/ijp.2023.72488.5275

Abstract
  Transcobalamin deficiency as a rare autosomal recessive disorder and methylmalonic acidemia is an autosomal recessive disorder of amino acid metabolism. Based on the common presentation ...  Read More
The Effectiveness of Parenteral Hydroxylcobalamin on Urine Mma in Children with Methylmalonic Acidemia
The Effectiveness of Parenteral Hydroxylcobalamin on Urine Mma in Children with Methylmalonic Acidemia

Afsane Nazari; Sepideh Bagheri; Zahra Abbasi Shaye; sara shirdelzade; Nafiseh Pourbadakhshan; peyman eshraghi

Volume 11, Issue 3 , March 2023, , Pages 17470-17476

https://doi.org/10.22038/ijp.2023.70401.5182

Abstract
  Background: Methylmalonic acidemia is a rare autosomal recessive disease in which there is a deficiency of intracellular cobalamin. This study aimed to assess the effectiveness of parenteral ...  Read More
The Effects of Enzyme Replacement Therapy in Patients with Mucopolysaccharidosis Type 1: A Case Series Study
The Effects of Enzyme Replacement Therapy in Patients with Mucopolysaccharidosis Type 1: A Case Series Study

Peyman Eshraghi; Majid Sezavar; Gholamreza Khademi; Anoush Azarfar; Shahabaldin Sorouri; Maryam Naseri

Volume 10, Issue 4 , April 2022, , Pages 15853-15864

https://doi.org/10.22038/ijp.2022.57113.4478

Abstract
  Background: Mucopolysaccharidosis type I (MPS1) is caused by mutations in the gene which encodes the enzyme alpha-L-iduronidase. Deficiency of this enzyme causes a range of clinical ...  Read More
Type 1 Tyrosinemia with Hypophosphatemic Rickets; a Case Report
Type 1 Tyrosinemia with Hypophosphatemic Rickets; a Case Report

Peyman Eshraghi; Foad Faroughi; Mohammad Karim Alizadeh

Volume 2, Issue 3.3 , September 2014, , Pages 63-66

https://doi.org/10.22038/ijp.2014.2999

Abstract
  Background: Tyrosinemia type 1 is an autosomal recessive metabolic disorder, which typically affects liver and kidneys. It is caused by a defect in fumarylacetoacetate hydrolase or ...  Read More
A Methylmalonic Acidemia Case Presenting with Acrodermatitis Enteropathica
A Methylmalonic Acidemia Case Presenting with Acrodermatitis Enteropathica

hesaneh izadyar; Peyman Eshraghi

Volume 2, Issue 3.2 , August 2014, , Pages 73-76

https://doi.org/10.22038/ijp.2014.2776

Abstract
  We encountered a patient with methylmalonic aciduria associated with skin lesions resembling acrodermatitis enteropathica. This child was being fed with a low-protein diet when the ...  Read More
Effectiveness of Group Cognitive-Behavioral Therapy on Anxiety, Depression and Glycemic Control in Children with Type 1 Diabetes
Effectiveness of Group Cognitive-Behavioral Therapy on Anxiety, Depression and Glycemic Control in Children with Type 1 Diabetes

Somaye Ahmadi; Zahra Tabibi; Ali Mashhadi; Peyman Eshraghi; Foad Faroughi; Parisa Ahmadi

Volume 2, Issue 3.1 , July 2014, , Pages 165-171

https://doi.org/10.22038/ijp.2014.2555

Abstract
  Introduction: The present study aimed to investigate the effectiveness of group cognitive behavioral therapy in reducing anxiety and depression and glycemic control in children with ...  Read More