Mahmoud F. Elsaid
Public Authority for Applied Education and Training(KW)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurogenetic and Muscular Disorders Research, Amyotrophic Lateral Sclerosis Research, Peripheral Neuropathies and Disorders, Epilepsy research and treatment
Most-Cited Works
- → Mutation in noncoding RNA RNU12 causes early onset cerebellar ataxia(2016)90 cited
- → Autosomal Recessive Inheritance of GLUT1 Deficiency Syndrome(2009)69 cited
- → Gene therapy for spinal muscular atrophy: the Qatari experience(2021)52 cited
- → A common mutation in theCBSgene explains a high incidence of homocystinuria in the Qatari population(2006)48 cited
- → AlteredPLP1splicing causes hypomyelination of early myelinating structures(2015)42 cited
- → Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant(2020)40 cited
- → Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy(2017)27 cited
- → W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report(2016)27 cited
- Recurrence risk after a first febrile convulsion.(2001)
- Acute bacterial meningitis in Qatar.(2006)