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)
Wiedemann-Steiner Syndrome with a 2-Year Follow-Up
Wiedemann-Steiner Syndrome with a 2-Year Follow-Up

Mohamad Hosein Mohamadi; Moein Mobini; Saba Vakili; Rahim Vakili

Volume 10, Issue 10 , October 2022, , Pages 16908-16913

https://doi.org/10.22038/ijp.2022.59825.4654

Abstract
  Wiedemann-Steiner syndrome (WDSTS) is an exceptionally rare genetic syndrome characterized by postnatal growth retardation, facial dysmorphism, hairy elbow, and short stature. It is ...  Read More
A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report
A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report

Amirsaeed Sabeti Aghabozorgi; Najmeh Ahangari; Moein Mobini; Rahim Vakili; Mohammad Doosti; Saba Vakili; Ehsan Ghayoor Karimiani

Volume 10, Issue 9 , September 2022, , Pages 16729-16737

https://doi.org/10.22038/ijp.2022.63946.4859

Abstract
  Background: Short stature is estimated to account for half of the new visits to pediatric endocrine practices. Therefore, evaluating its underlying causes seems essential in order to ...  Read More
Prevalence of Testicular Adrenal Rest Tumor and Factors Associated with its Development in 6 Months to 18 Years-old Patients with Congenital Adrenal Hyperplasia
Prevalence of Testicular Adrenal Rest Tumor and Factors Associated with its Development in 6 Months to 18 Years-old Patients with Congenital Adrenal Hyperplasia

Samaneh Norooziasl; zhila afshar; Nosrat Ghaemi; Rahim Vakili; Seyed Ali Alamdaran; Zahra Abbasi Shaye; Peyman Eshraqhi; Nasrin Moazzen

Volume 9, Issue 12 , December 2021, , Pages 15022-15028

https://doi.org/10.22038/ijp.2021.57453.4511

Abstract
  Background: Congenital adrenal hyperplasia (CAH) is a potentially life-threatening form of primary adrenal insufficiency characterized by cortisol, aldosterone, and epinephrine deficiencies, ...  Read More
Tyrosinemia Type III: A Case Report with a Seven Years Follow-up
Tyrosinemia Type III: A Case Report with a Seven Years Follow-up

Saba Vakili; Mohammadreza Emami; Moein Mobini; Rahim Vakili

Volume 9, Issue 6 , June 2021, , Pages 13853-13857

https://doi.org/10.22038/ijp.2021.56791.4451

Abstract
  Hereditary tyrosinemia type III (OMIM 276710) is a rare inborn error of tyrosine metabolism caused by the deficiency of 4-hydroxyphenylpyruvate dioxygenase (HPD). This ...  Read More
Thyroid Disorders in Pediatric Patients with Turner Syndrome; A 16 Years' Experience
Thyroid Disorders in Pediatric Patients with Turner Syndrome; A 16 Years' Experience

Moein Mobini; reza Jafarzadeh Esfehani; Saba Vakili; Ahmadreza Zarifian; Rahim Vakili

Volume 9, Issue 5 , May 2021, , Pages 13503-13513

https://doi.org/10.22038/ijp.2021.56094.4411

Abstract
  Background Turner syndrome patients are more likely to develop autoimmune diseases in contrast to the general population. Many research have had controversial results suggest a possible ...  Read More
The Relation between Karyotype Findings and Gonadotropin Levels in Pediatric Turner’s syndrome Patients
The Relation between Karyotype Findings and Gonadotropin Levels in Pediatric Turner’s syndrome Patients

Fatemeh Zarei; Moein Mobini; reza Jafarzadeh Esfehani; Maryam Khalesi; Rahim Vakili

Volume 9, Issue 2 , February 2021, , Pages 13005-13011

https://doi.org/10.22038/ijp.2020.54327.4296

Abstract
  Background Abnormal pubertal development and fertility are among the frequent complications in Turner’s syndrome. Although elevated level of gonadotropins in Turner’s syndrome ...  Read More
Gyrate Atrophy of the Choroid and Retina: A Case Report
Gyrate Atrophy of the Choroid and Retina: A Case Report

Somayyeh Hashemian; Rahim Vakili; Azadeh Zare Feizabadi

Volume 7, Issue 9 , September 2019, , Pages 10119-10123

https://doi.org/10.22038/ijp.2019.36478.3179

Abstract
  Introduction Gyrate atrophy of the choroid and retina is a metabolic disorder, which is inherited in an autosomal recessive pattern. Although gyrate atrophy is rare, it is concerning ...  Read More
Mccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review
Mccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review

Rahim Vakili; Somayyeh Hashemian; Reza Jafarzadeh Esfehani; Azadeh Zare Feizabadi

Volume 7, Issue 5 , May 2019, , Pages 9453-9459

https://doi.org/10.22038/ijp.2019.36513.3181

Abstract
  McCune-Albright Syndrome (MAS) is a rare sporadic disease characterized by bone fibrous dysplasia, Café au lait spots and a variable association of hyperfunction endocrine ...  Read More
Papillary Carcinoma Thyroid in a Nine-year-old Child: A Case Report
Papillary Carcinoma Thyroid in a Nine-year-old Child: A Case Report

Ali Alamdaran; Rahim Vakili; Somayyeh Hashemian; Asma Javid

Volume 6, Issue 8 , August 2018, , Pages 8015-8019

https://doi.org/10.22038/ijp.2018.29043.2541

Abstract
        Thyroid enlargement and nodules are very rare in children, but when they occur, the chance of malignancy among these nodules is very high. Thyroid carcinoma ...  Read More
4-Hydroxybutyric Aciduria as a Rare Presentation of Global Developmental Delay in Children: Case Report of Two Different Patients
4-Hydroxybutyric Aciduria as a Rare Presentation of Global Developmental Delay in Children: Case Report of Two Different Patients

Rahim Vakili; Mehran Beiraghi Toosi; Asma Javid; Nahid Donyadideh; Farnoosh Ebrahimzadeh; Narges Hashemi; Somayeh Hashemian

Volume 6, Issue 7 , July 2018, , Pages 7861-7865

https://doi.org/10.22038/ijp.2018.27462.2367

Abstract
  Succinic semialdehyde dehydrogenase (SSADH) deficiency or 4-Hydroxybutyric Aciduria is an autosomal recessive inherited disorder of amma-aminobutyric acid (GABA) degradation. It ...  Read More
Lingual Thyroid: A Case Report and Literature Review
Lingual Thyroid: A Case Report and Literature Review

Somayeh Hashemian; Peyman Eshraqhi; Rahim Vakili; Mahdi Behnam

Volume 5, Issue 11 , November 2017, , Pages 6049-6055

https://doi.org/10.22038/ijp.2017.24949.2109

Abstract
  Thyroid ectopia is a dysgenesis of thyroid gland and Lingual position represents the most frequent ectopic location accounting up to 90% of ectopic cases. Hypothyroidism is commonly ...  Read More
Black Urine
Black Urine

Rahim Vakili; Parisa Armanpoor; Parvaneh Armanpoor

Volume 4, Issue 6 , June 2016, , Pages 1857-1858

https://doi.org/10.22038/ijp.2016.6860

Abstract
  A 2-year-old boy was born at term of healthy, non-consanguineous Iranian parents. His mother attended in the clinic with the history of sometimes discoloration of diapers after passing ...  Read More
Immunization Coverage in WHO Regions: A Review Article
Immunization Coverage in WHO Regions: A Review Article

Rahim Vakili; Amirhosein Ghazizadeh Hashemi; Gholamreza Khademi; Maryam Ajilian Abbasi; Masumeh Saeidi

Volume 3, Issue 2.1 , March 2015, , Pages 111-118

https://doi.org/10.22038/ijp.2015.4157

Abstract
    In 1974, the World Health Organization (WHO) established the Expanded Program on Immunization (EPI) to ensure that all children have access to routinely recommended ...  Read More
McCune-Albright Syndrome: A Case Report and Literature Review
McCune-Albright Syndrome: A Case Report and Literature Review

Moein Mobini; Rahim Vakili; Saba Vakili

Volume 2, Issue 2.2 , April 2014, , Pages 153-156

https://doi.org/10.22038/ijp.2014.2416

Abstract
  McCune-Albright syndrome (MAS) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. The disorder is more common in females and is characterized by a triad ...  Read More
Maternal Knowledge and Attitude toward Exclusive Breast Milk Feeding (BMF) in the First 6 Months of Infant Life in Mashhad
Maternal Knowledge and Attitude toward Exclusive Breast Milk Feeding (BMF) in the First 6 Months of Infant Life in Mashhad

Bibi Leila Hoseini; Rahim Vakili; Mohammad Ali Kiani; Ali Khakshour; Masumeh Saeidi

Volume 2, Issue 1 , January 2014, , Pages 63-69

https://doi.org/10.22038/ijp.2014.2122

Abstract
  Introduction: Breast milk is a complete food for growing children until 6 months of age, and mothers, as the most important child health care, play a decisive role in their growth. ...  Read More
Congenital Rickets: Report of Four Cases
Congenital Rickets: Report of Four Cases

Rahim Vakili; Peyman Eshraghi; Alireza Ataei Nakhaei; Saba Vakili; Ali Khakshour; Masumeh Saeidi; Behjat Zarif; Somayeh Nateghi

Volume 2, Issue 1 , January 2014, , Pages 101-105

https://doi.org/10.22038/ijp.2014.2128

Abstract
  Introduction: Vitamin D deficiency and rickets continue to be health problems in developing countries and most of the infants with congenital rickets may present with hypocalcemic seizure. ...  Read More
Assessment the Relationship Between Parents' Literacy Level with Children Growth in Mashhad: An Analytic Descriptive Study
Assessment the Relationship Between Parents' Literacy Level with Children Growth in Mashhad: An Analytic Descriptive Study

Masumeh Saeidi; Rahim Vakili; Bibi Leila Hoseini; Ali Khakshour; Behjat Zarif; Somayeh Nateghi

Volume 1, Issue 2 , December 2013, , Pages 39-43

https://doi.org/10.22038/ijp.2013.2258

Abstract
  Introduction: Present children are the investments of community in the future. Preparing children health which leads to the stability of community health, provided to accurate implementation ...  Read More
Precocious Puberty: An Unusual Presentation of Hypothyroidism
Precocious Puberty: An Unusual Presentation of Hypothyroidism

Nosrat Ghaemi; Rahim Vakili; Sepideh Bagheri

Volume 1, Issue 2 , December 2013, , Pages 51-54

https://doi.org/10.22038/ijp.2013.2165

Abstract
  Hypothyroidism is usually associated with delayed pubertal development but in rare occasions precocious puberty may ensue which is seen in cases of prolonged and untreated hypothyroidism. ...  Read More
Iron and Multivitamin Supplements in Children and its Association with Growth rate
Iron and Multivitamin Supplements in Children and its Association with Growth rate

Masumeh Saeidi; Rahim Vakili; Ali Khakshour; Habibolah Taghizadeh Moghaddam; Mohammad Ali Kiani; Behjat Zarif; Somayeh Nateghi

Volume 1, Issue 1 , August 2013, , Pages 13-17

https://doi.org/10.22038/ijp.2013.2028

Abstract
  Introduction: Vitamin deficiency and iron deficiency anemia are common nutritional problems, at least in children under 5. These materials shortage, especially in the first two years ...  Read More