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Journal of Neurogenetics|July 9, 2017
LGMD2E is the most common type of sarcoglycanopathies in the Iranian populationAfagh Alavi, Sara Esmaeili, Yalda Nilipour, et al.Epilepsy & Behavior Reports|December 1, 2025
A case of neurosarcoidosis presenting as hippocampal sclerosis: Clinicopathological correlation and proposed mechanistic linkElham Rahimian, Guive Sharifi, Hans Jürgen Huppertz, et al.Iranian Journal of Cancer Prevention|January 29, 2015
Survey on childhood solid malignant tumors in cases admitted to mofid pediatric hospital from 1996-2010: a single-center studyFarzaneh Jadali, Hosein Aghayan Golkashani, Golareh Habibi, et al.Human Genetics|November 10, 2012
Identification of COL6A2 mutations in progressive myoclonus epilepsy syndromeSiamak Karkheiran, Catharine E Krebs, Vladimir Makarov, et al.Journal of Magnetic Resonance Imaging : JMRI|November 30, 2023
Glioma Tumor Grading Using Radiomics on Conventional MRI: A Comparative Study of WHO 2021 and WHO 2016 Classification of Central Nervous TumorsFarzan Moodi, Fereshteh Khodadadi Shoushtari, Delaram J Ghadimi, et al.Gastroenterology and Hepatology From Bed to Bench|April 19, 2021
Increased regulatory T cells in peripheral blood of children with eosinophilic esophagitisMahnaz Abdolahi, Shima Rasouli, Delara Babaie, et al.Frontiers in Neurology|October 8, 2021
Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian ConsensusFarzad Fatehi, Mahmoud Reza Ashrafi, Marzieh Babaee, et al.BMC Neurology|October 17, 2015
Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group, Fatma Al Jasmi, Mohammed Al Jumah, et al.Neurobiology of Aging|November 15, 2020
BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genesMarzieh Khani, Hosein Shamshiri, Hanieh Taheri, et al.Human Molecular Genetics|February 5, 2019
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24Carola Hedberg-Oldfors, Alexandra Abramsson, Daniel P S Osborn, et al.Pageof 7