Hatem Murad

Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C > T

Salma M. Wakil, Khushnooda Ramzan, Rula Abuthuraya et al. · Gene · 2013 · 32 citations

Life Sciences, Genetics, Neurology +14

Chorea‐acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula

Saeed Bohlega, Adel A. AlJishi, Carol Dobson‐Stone et al. · Movement Disorders · 2002 · 24 citations

Life Sciences, Genetics, Pathology +15

Clinical and genetic features of anoctaminopathy in Saudi Arabia

Saeed Bohlega, Dorothy M. Monies, Ahmad Abulaban et al. · Neurosciences · 2015 · 21 citations · Full text

Medicine, Genetics, Pathology +15

Total innervation of the extensor digitorum brevis by the accessory deep peroneal nerve

Hatem Murad, Peggy Neal, Bashar Katirji · European Journal of Neurology · 1999 · 19 citations · Full text

Medicine, Anatomy, Orthopaedic Surgery +10

Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia

Norah Alharbi, Rawan Matar, Edward Cupler et al. · Frontiers in Neuroscience · 2022 · 15 citations · Full text

Life Sciences, Genetics, Neurology +14