Mahmoud F. Elsaid

Mutation in noncoding <scp>RNA RNU12</scp> causes early onset cerebellar ataxia

Mahmoud F. Elsaid, Nader Chalhoub, Tawfeg Ben‐Omran et al. · Annals of Neurology · 2016 · 89 citations

Autosomal Recessive Inheritance of GLUT1 Deficiency Syndrome

Jörg Klepper, Hans Scheffer, Mahmoud F. Elsaid et al. · Neuropediatrics · 2009 · 69 citations

Down Syndrome, Sporadic Transmission, Developmental Biology +11

Gene therapy for spinal muscular atrophy: the Qatari experience

Hossamaldein Gaber Ali, Khalid Ibrahim, Mahmoud F. Elsaid et al. · Gene Therapy · 2021 · 49 citations · Full text

A common mutation in the<i>CBS</i>gene explains a high incidence of homocystinuria in the Qatari population

Mahmoud F. Elsaid, Ramin Badii, Mohammed Bessisso et al. · Human Mutation · 2006 · 48 citations

Genetics, Qatari Population, Genetic Epidemiology +16

Altered<i>PLP1</i>splicing causes hypomyelination of early myelinating structures

Sietske H. Kevelam, Jennifer R. Taube, Rosalina M.L. van Spaendonk et al. · Annals of Clinical and Translational Neurology · 2015 · 41 citations · Full text