Pegah Ghandil

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2021
Publications (10 Years): 5

Top Topics

Interstitial Lung Disease

Top Venues

Journal of clinical laboratory analysis

The journal of gene medicine

Journal of diabetes and metabolic disorders

This page only lists publications with an associated author ORCID identifier.

Publications

Fatemeh Davoudi, Majid Aminzadeh, Hajiye Bibi Shahbazian, Mahdi Bijanzadeh, Ata A Ghadiri, Pegah Ghandil
Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management. Journal of diabetes and metabolic disorders 20 (2) (2021)
Atefeh Heydari, Farhad Abolnezhadian, Mahnaz Sadeghi-Shabestari, Alihossein Saberi, Ahmad Shamsizadeh, Ata A Ghadiri, Pegah Ghandil
Identification of Cytochrome b-245, beta-chain gene mutations, and clinical presentations in Iranian patients with X-linked chronic granulomatous disease. Journal of clinical laboratory analysis 35 (2) (2020)
Malihe Mohamadian, Mohsen Naseri, Pegah Ghandil, Afsane Bahrami, Ali Akbar Momen
The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes. The journal of gene medicine 22 (12) (2020)
Mahzad Nasirshalal, Maryam Tahmasebi Birgani, Mohammadreza Dadfar, Roshan Nikbakht, Alihossein Saberi, Pegah Ghandil
Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men. Andrologia 52 (11) (2020)
Malihe Mohamadian, Pegah Ghandil, Mohsen Naseri, Afsane Bahrami, Ali Akbar Momen
A novel homozygous variant in an Iranian pedigree with cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4. Journal of clinical laboratory analysis 34 (11) (2020)