Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging SpectraMahmoud Reza Ashrafi, Zahra Rezaei, Reza Azizi Malamiri et al.|The Cerebellum|2022Cited by 7
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoud Reza Ashrafi, Masoud Garshasbi, Reyhaneh Kameli et al.|Neurogenetics|2023Cited by 4
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Mahmoud Reza Ashrafi, Morteza Heidari et al.|Human Genomics|2024Cited by 4
Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoud Reza Ashrafi, Masoud Garshasbi, Reyhaneh Kameli et al.|Neurogenetics|2023Cited by 0