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, Mohammad Rohani et al.|The Cerebellum|2022Cited by 7
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
A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophiesSareh Hosseinpour, Ali Reza Tavasoli, Ehsan Razmara et al.|Brain and Development|2023Cited by 2