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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Diagnosis and management of Neuro-Behçet’s disease: international consensus recommendationsKalra, Seema ; Silman, Alan ; Akman-Demir, Gulsen ; Bohlega, Saeed ; Borhani-Haghighi, Afshin ; Constantinescu, Cris S. ; Houman, Habib ; Mahr, Alfred ; Salvarani, Carlos ; Sfikakis, Petros P. ; Siva, Aksel ; Al-Araji, AdnanJournal of neurology, 2014-09, Vol.261 (9), p.1662-1676 [Periódico revisado por pares]Texto completo disponível |
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4 |
Material Type: Artigo
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Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)Abusrair, Ali ; Bohlega, SaeedNeurology, 2019-04, Vol.92 (15_supplement) [Periódico revisado por pares]Texto completo disponível |
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5 |
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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6 |
Material Type: Artigo
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Cerebrotendinous xanthomatosis: A candidate for ACMG list of secondary findings?Khouj, Ebtissal ; Bohlega, Saeed ; Alkuraya, Fowzan S.Clinical genetics, 2023-01, Vol.103 (1), p.125-126 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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7 |
Material Type: Artigo
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Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)Bohlega, Saeed ; Al-Qahtani, Zainah ; Guzmán-Vega, Francisco J. ; Ramakrishnan, Reshmi ; Abusrair, Ali ; Aldosari, Haya ; AlDakheel, Amaal ; Al-Qahtani, Salma ; Monies, Dorota ; Arold, StefanNeurology, 2023-04, Vol.100 (17_supplement_2) [Periódico revisado por pares]Texto completo disponível |
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8 |
Material Type: Artigo
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Multiple sclerosis in the Arabian Gulf countries: a consensus statementBohlega, Saeed ; Inshasi, Jihad ; Al Tahan, Abdel Rahman ; Madani, Abu Bakr ; Qahtani, Hussien ; Rieckmann, PeterJournal of neurology, 2013-12, Vol.260 (12), p.2959-2963 [Periódico revisado por pares]Berlin/Heidelberg: Springer Berlin HeidelbergTexto completo disponível |
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9 |
Material Type: Artigo
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Brain MRI findings in Woodhouse-Sakati Syndrome (P6.071)Abusrair, Ali ; Bohlega, Saeed ; Al-Ajlan, Fahad ; Al-Semari, Abdulaziz ; Mohamed, Bader ; AlDakheel, AmaalNeurology, 2018-04, Vol.90 (15_supplement) [Periódico revisado por pares]Texto completo disponível |
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10 |
Material Type: Artigo
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SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3Alazami, Anas M ; Alzahrani, Fatema ; Bohlega, Saeed ; Alkuraya, Fowzan SNeurology, 2014-05, Vol.82 (18), p.1665-1666 [Periódico revisado por pares]United States: American Academy of NeurologyTexto completo disponível |