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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Torticollis: A Presenting Sign in Idiopathic Intracranial HypertensionBohlega, S ; Idriss, AAnnals of Saudi medicine, 1997-03, Vol.17 (2), p.260-261, Article 260 [Periódico revisado por pares]Saudi ArabiaTexto completo disponível |
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2 |
Material Type: Resenha
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The Burden of Musculoskeletal Conditions at the Start of the New MillenniumBohlega, SaeedAnnals of Saudi Medicine, 2004, Vol.24 (5), p.403-404 [Periódico revisado por pares]King Faisal Specialist Hospital and Research CentreTexto completo disponível |
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3 |
Material Type: Artigo
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The Burden of Musculoskeletal Conditions at the Start of the New MillenniumReport of a WHO Scientific Group. 2004, 218 pages. World Health Organization, Technical Report Series, No. 919, ISBN 92 4 120919 4Bohlega, SaeedAnnals of Saudi medicine, 2004-09, Vol.24 (5), p.403-404 [Periódico revisado por pares]Texto completo disponível |
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4 |
Material Type: Artigo
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CADASIL in Arabs: clinical and genetic findingsBohlega, Saeed ; Al Shubili, Asmahan ; Edris, Abdulrahman ; Alreshaid, Abdulrahman ; Alkhairallah, Thamer ; AlSous, M Walid ; Farah, Samir ; Abu-Amero, Khaled KBMC medical genetics, 2007-11, Vol.8 (1), p.67-67, Article 67 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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5 |
Material Type: Artigo
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Absence of mtDNA mutations in leukocytes of CADASIL patientsAbu-Amero, Khaled K ; Hellani, Ali ; Bohlega, SaeedBMC research notes, 2008-05, Vol.1 (1), p.16-16 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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6 |
Material Type: Artigo
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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case reportAbu-Amero, Khaled K ; Al-Dhalaan, Hesham ; Bohlega, Saeed ; Hellani, Ali ; Taylor, Robert WJournal of medical case reports, 2009-10, Vol.3 (1), p.77-77, Article 77 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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7 |
Material Type: Artigo
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Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi ArabiaBohlega, Saeed A ; Shinwari, Jameela M ; Al Sharif, Latifa J ; Khalil, Dania S ; Alkhairallah, Thamer S ; Al Tassan, Nada ABMC medical genetics, 2011-02, Vol.12 (1), p.27-27, Article 27 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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8 |
Material Type: Artigo
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Novel mutation of the NOTCH3 gene in Arabic family with CADASILBohlega, SaeedNeurology international, 2011-04, Vol.3 (1) [Periódico revisado por pares]Texto completo disponível |
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9 |
Material Type: Artigo
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Novel mutation of the notch3 gene in arabic family with CADASILBohlega, SaeedNeurology international, 2011-07, Vol.3 (2), p.e6-e6 [Periódico revisado por pares]Italy: MDPI AGTexto completo disponível |
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10 |
Material Type: Artigo
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Future of Management of Multiple Sclerosis in the Middle East: A Consensus View from Specialists in Ten CountriesAljumah, Mohammed ; Alroughani, Raed ; Alsharoqi, I. ; Bohlega, Saeed A. ; Dahdaleh, Maurice ; Deleu, Dirk ; Esmat, Khaled ; Khalifa, Ahmad ; Sahraian, Mohammad A. ; Szólics, Miklós ; AlTahan, Abdulrahman ; Yamout, Bassem I. ; Rieckmann, Peter ; Daif, Abdulkader Bruck, Wolfgang ; Wolfgang BruckMultiple Sclerosis International, 2013-01, Vol.2013, p.952321-6 [Periódico revisado por pares]Egypt: Hindawi LimitedsTexto completo disponível |