M. Salih

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.

N. Drouot, A. Durr, L. Schöls, 2009, Brain : a journal of neurology.

Genetic and phenotypic characterization of NKX6‐2‐related spastic ataxia and hypomyelination

Nancy T. Malintan, N. Wood, A. Chiriță-Emandi, 2019, European journal of neurology.

Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their Significance

A. Barkovich, A. Poduri, M. Salih, 2011, American Journal of Neuroradiology.