Zahra Rezaei

Follow‐up of 25 patients with treatable ataxia: A comprehensive case series study

M. Rohani, A. Tavasoli, M. Heidari, 2022, Clinical case reports.

Expanding the genetic spectrum of giant axonal neuropathy: Two novel variants in Iranian families

N. Mahdieh, A. Tavasoli, Pouria Mohammadi, 2023, Molecular genetics & genomic medicine.

The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy.

A. Fayyazi, M. Barzegar, F. Fatehi, 2023, Journal of neuromuscular diseases.

Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

M. Garshasbi, Shaghayegh Zokaei, M. Rohani, 2023, Orphanet Journal of Rare Diseases.

The effect of normalizing vaginal microbiome using Lactovag in improving pregnancy outcomes in frozen embryo transfer cycles: a randomized clinical trial

F. A. Asbagh, Zahra Rezaei, F. Tanha, 2023, Archives of Gynecology and Obstetrics.

The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population

M. Synofzik, S. Zuchner, M. Garshasbi, 2024, Human genomics.

Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry

M. Garshasbi, Ali Hosseini Bereshneh, M. Rohani, 2023, neurogenetics.

High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry

M. Barzegar, M. Garshasbi, Ali Hosseini Bereshneh, 2023, neurogenetics.