A novel variant of Paganini-Miozzo syndrome: a case report

por Sarmadian, Roham, Gilani, Abolfazl, Biglari, Habibe Nejad
Publicado 2023

A Rare Case of Cerebrotendinous Xanthomatosis Associated With a Mutation on COG8 Gene

por Ghoshouni, Hamed, Sarmadian, Roham, Irilouzadian, Rana, Biglari, Habibe Nejad, Gilani, Abolfazl
Publicado 2023

An unusual case of a toddler with Canavan disease with frequent intractable seizures: A case report and review of the literature

por Irilouzadian, Rana, Goudarzi, Ali, Hesami, Hamed, Sarmadian, Roham, Biglari, Habibe Nejad, Gilani, Abolfazl
Publicado 2023