original article
An Investigation of Basic Needs and Related Factors in Parents of Children with Down syndrome
An Investigation of Basic Needs and Related Factors in Parents of Children with Down syndrome

Mohsen Mohammadi; Parichehr Shahroudi; Yasaman Yaghobi; Parinaz Shahroudi; Saman Maroufizadeh; Zahra Golamalipour

Volume 11, Issue 7 , July 2023, Pages 18018-18026

https://doi.org/10.22038/ijp.2023.73176.5303

Abstract
  Background: Down syndrome is one of the most common causes of intellectual disabilities in children. The birth of a baby requires a positive adaptation of the family to new changes, ...  Read More
original article
Risk of Neonatal Outcomes Associated with COVID-19 Infection during Pregnancy: A Retrospective Cohort Study
Risk of Neonatal Outcomes Associated with COVID-19 Infection during Pregnancy: A Retrospective Cohort Study

Maliheh Mahmoudinia; Tahereh Sadeghi; Nadia Sheikhi; Mahdi Niknazar; Faezeh Zakerinasab

Volume 11, Issue 7 , July 2023, Pages 18027-18036

https://doi.org/10.22038/ijp.2023.72990.5295

Abstract
  Background: Since its announcement as a pandemic, COVID-19 has been shown to be associated with more severe outcomes among pregnant women. Infected mothers may develop Intrauterine ...  Read More
original article
Abnormal EEG in Autistic Patients without Any History of Clinical Seizures
Abnormal EEG in Autistic Patients without Any History of Clinical Seizures

Hasan Golmakani; Farhad Heydarian; Majid Khademian; Somayyeh Mahdavikia

Volume 11, Issue 7 , July 2023, Pages 18037-18043

https://doi.org/10.22038/ijp.2023.71097.5219

Abstract
  Background: There is insufficient information regarding whether epileptic manifestations, in the absence of seizures, contribute to the development of autism symptoms. Electroencephalography ...  Read More
original article
Synbiotic supplementation in type one diabetes mellitus: A Randomized Controlled Clinical Trial
Synbiotic supplementation in type one diabetes mellitus: A Randomized Controlled Clinical Trial

Setila Dalili; Ghazaleh Sadat Aldaghi; Shahin Koohmanaee; Maryam Shahrokhi; Mohammad Ali Esfandiari; Seyed Amirreza Nemati; Jafar Aldaghi; Afagh Hassanzadeh Rad; Houman Hashemian

Volume 11, Issue 7 , July 2023, Pages 18044-18054

https://doi.org/10.22038/ijp.2023.72204.5262

Abstract
  Background: limited studies have been conducted on the effect of synbiotics supplementation on Type 1 Diabetes Mellitus (T1DM). The current study aimed to evaluate the impacts of synbiotic ...  Read More
original article
An Evaluation of Predictive Factors for Pulmonary Valve Replacement after Total Correction in Children with tetralogy of Fallot
An Evaluation of Predictive Factors for Pulmonary Valve Replacement after Total Correction in Children with tetralogy of Fallot

Akbar Molaei; Maedeh Geybei; Shamsi Ghaffari; Shahram Sadeghvand; MirHadi Mousavi; Ahmad Jamei Khosroshahi

Volume 11, Issue 7 , July 2023, Pages 18055-18067

https://doi.org/10.22038/ijp.2023.69660.5141

Abstract
  Background: Congenital heart defects, with a prevalence of 4-8 cases per 1000 births, are one of the most common congenital defects. Tetralogy of Fallot (ToF) is the most common congenital ...  Read More
original article
Investigating the Severity of Lung Disease Using Lung CT Scan and Pulmonary Function Tests in Children with Cystic Fibrosis
Investigating the Severity of Lung Disease Using Lung CT Scan and Pulmonary Function Tests in Children with Cystic Fibrosis

babak Kabir; Dayan Amanian; Narges Lashkarbolouk; Mahdi Mazandarani; Lobat Shahkar

Volume 11, Issue 7 , July 2023, Pages 18068-18076

https://doi.org/10.22038/ijp.2023.72804.5286

Abstract
  Background: Cystic Fibrosis (CF) is an autosomal recessive disease that has a negative impact on the quality of life in patients. Various methods for assessing lung function and airway ...  Read More
letter to the editor
Oral Health Change in Iran: Part V; It Is the Time to Focus on MIH by an Electronic Approach - Letter to the Editor
Oral Health Change in Iran: Part V; It Is the Time to Focus on MIH by an Electronic Approach - Letter to the Editor

Somayeh Hekmatfar; Hossein Hessari; Karim Jafari Kaffash; Fatemeh Darabi; Shadi Kaffashchian; Masoud Shabani

Volume 11, Issue 7 , July 2023, Pages 18077-18079

https://doi.org/10.22038/ijp.2023.72807.5287

Abstract
  Periodic data for determining the DMFT index in 12-year-old children showed that the index had a significant improvement in different periods of its measurement during 25 years after ...  Read More
systematic review
Prevalence of Diabetic Nephropathy in Patients with Type 1 Diabetes in Iran: A Systematic Review and Meta-Analysis
Prevalence of Diabetic Nephropathy in Patients with Type 1 Diabetes in Iran: A Systematic Review and Meta-Analysis

Behzad Darabi; Maryam Alemzadeh; Saba Sardari

Volume 11, Issue 7 , July 2023, Pages 18080-18088

https://doi.org/10.22038/ijp.2023.70827.5206

Abstract
  Background: Diabetic nephropathy (DN) is one of the complications of diabetes. The present study was conducted with the aim of determining the prevalence of DN in patients with D1T ...  Read More
review article
Nutritional Aspects in Immunocompromised Patients
Nutritional Aspects in Immunocompromised Patients

Nasrin Moazzen; Asma Afshari; Saeedeh Talebi

Volume 11, Issue 7 , July 2023, Pages 18089-18098

https://doi.org/10.22038/ijp.2023.73627.5323

Abstract
  With the rise in life expectancy, there has been an increase in the population with immune deficiency. This necessitates the need to find ways to improve the quality of life and survival ...  Read More
case report
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