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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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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3 |
Material Type: Artigo
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Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL familyAl-Shaar, Hussam Abou ; Qadi, Najeeb ; Ahmed, Mohammed ; Meyer, Brian F ; Bohlega, SaeedJournal of the neurological sciences, 2016-08, Vol.367, p.239-243 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |
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4 |
Material Type: Artigo
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Neurological complications in liver transplantationGHAUS, Naveed ; BOHLEGA, Saeed ; REZEIG, MohammedJournal of neurology, 2001-12, Vol.248 (12), p.1042-1048 [Periódico revisado por pares]Berlin: SpringerTexto completo disponível |
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5 |
Material Type: Artigo
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Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological featuresCupler, Edward J ; Bohlega, Saeed ; Hessler, Richard ; McLean, Donald ; Stigsby, Bent ; Ahmad, JavedNeuromuscular disorders : NMD, 1998-06, Vol.8 (5), p.321-326 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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6 |
Material Type: Artigo
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Neurodegenerative Huntington-like disorderBohlega, Saeed ; Al-Tahan, Abdulrahman ; Kambouris, Marios ; Divakaran, MadaiMovement disorders, 2001-05, Vol.16 (3), p.533-534 [Periódico revisado por pares]New York: John Wiley & Sons, IncTexto completo disponível |
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7 |
Material Type: Artigo
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T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson DiseaseChishti, Muhammad A ; Bohlega, Saeed ; Ahmed, Maqbool ; Loualich, Arslan ; Carroll, Pamela ; Sato, Christine ; St George-Hyslop, Peter ; Westaway, David ; Rogaeva, EkaterinaArchives of neurology (Chicago), 2006-10, Vol.63 (10), p.1483-1485Chicago, IL: American Medical AssociationTexto completo disponível |
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8 |
Material Type: Artigo
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Subacute sclerosing panencephalitis: evaluation with CT and MRBrismar, J ; Gascon, GG ; von Steyern, KV ; Bohlega, SAmerican journal of neuroradiology : AJNR, 1996-04, Vol.17 (4), p.761-772 [Periódico revisado por pares]Oak Brook, IL: Am Soc NeuroradiologyTexto completo disponível |
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9 |
Material Type: Artigo
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Impact of the first Gulf war on multiple sclerosis risk in Kuwait: a quasi-experimental studyAkhtar, Saeed ; Al-Hashel, Jasem Y ; Alroughani, RaedBMC neurology, 2023-07, Vol.23 (1), p.259-259, Article 259 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |