Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosisAl-Saif, Amr ; Al-Mohanna, Futwan ; Bohlega, SaeedAnnals of neurology, 2011-12, Vol.70 (6), p.913-919 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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2 |
Material Type: Artigo
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Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and MigraineMarashly, Eyad T ; Bohlega, Saeed AFrontiers in neurology, 2017-07, Vol.8, p.333-333 [Periódico revisado por pares]Switzerland: Frontiers Media S.ATexto completo disponível |
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3 |
Material Type: Artigo
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Multimodal Evoked Potential Profiles in Woodhouse-Sakati SyndromeAbusrair, Ali ; AlHamoud, Iftetah ; Bohlega, SaeedJournal of clinical neurophysiology, 2022-09, Vol.Publish Ahead of Print (6), p.504-509 [Periódico revisado por pares]United StatesTexto completo disponível |
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4 |
Material Type: Artigo
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Loss of ERLIN2 function leads to juvenile primary lateral sclerosisAl-Saif, Amr ; Bohlega, Saeed ; Al-Mohanna, FutwanAnnals of neurology, 2012-10, Vol.72 (4), p.510-516 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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5 |
Material Type: Artigo
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Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 MutationAlqwaifly, Mohammed ; Bohlega, SaeedNeurology international, 2016-06, Vol.8 (2), p.6444-6444 [Periódico revisado por pares]Italy: MDPI AGTexto completo disponível |
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6 |
Material Type: Artigo
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Genetic of Parkinson’s disease among arabsBohlega, S.Journal of the neurological sciences, 2017-10, Vol.381, p.17-17 [Periódico revisado por pares]Elsevier B.VTexto completo disponível |
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7 |
Material Type: Artigo
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Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissuesBohlega, Saeed ; Al-Ajlan, Huda ; Al-Saif, AmrEuropean journal of human genetics : EJHG, 2014-05, Vol.22 (5), p.640-643 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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8 |
Material Type: Artigo
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Epidemiology of MSBohlega, SaeedMultiple sclerosis and related disorders, 2014-11, Vol.3 (6), p.766-767Elsevier B.VTexto completo disponível |
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9 |
Material Type: Artigo
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Ceroid lipofuscinosis type 5 (CLN5) gene mutation associated adult-onset cerebellar ataxiaAbusrair, A. ; Bohlega, S. ; Wakil, S.Journal of the neurological sciences, 2019-10, Vol.405, p.111-111 [Periódico revisado por pares]Elsevier B.VTexto completo disponível |
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10 |
Material Type: Artigo
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Juvenile onset parkinsonism-dystonia syndrome: A novel mutation in the SLC6A3 geneAbusrair, A. ; Bohlega, S. ; Wakil, S.Journal of the neurological sciences, 2019-10, Vol.405, p.333-334 [Periódico revisado por pares]Elsevier B.VTexto completo disponível |