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)
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