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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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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2 |
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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3 |
Material Type: Artigo
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Unilateral pallidotomy for hemidystoniaAlkhani, Ahmed ; Bohlega, SaeedMovement disorders, 2006-06, Vol.21 (6), p.852-855 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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4 |
Material Type: Artigo
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Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsulaBohlega, Saeed ; Al-Jishi, Adel ; Dobson-Stone, Carol ; Rampoldi, Luca ; Saha, Parthasarathi ; Murad, Hatem ; Kareem, Abid ; Roberts, George ; Monaco, Anthony P.Movement disorders, 2003-04, Vol.18 (4), p.403-407 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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5 |
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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6 |
Material Type: Artigo
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A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxiaAl Tassan, Nada ; Khalil, Dania ; Shinwari, Jameela ; Al Sharif, Latifa ; Bavi, Prashant ; Abduljaleel, Zainularifeen ; Abu Dhaim, Nada ; Magrashi, Amna ; Bobis, Steve ; Ahmed, Hala ; AlAhmed, Samaher ; Bohlega, SaeedHuman mutation, 2012-02, Vol.33 (2), p.351-354 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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7 |
Material Type: Artigo
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Hemiplegia caused by inadvertent intra-carotid infusion of total parenteral nutritionBohlega, Saeed ; McLean, Donald R.Clinical neurology and neurosurgery, 1997-08, Vol.99 (3), p.217-219 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |
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8 |
Material Type: Artigo
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Guillain-Barré syndrome with severe demyelination mimicking axonopathyBohlega, Saeed A. ; Stigsby, Bent ; Haider, A. ; McLean, DonaldMuscle & nerve, 1997-04, Vol.20 (4), p.514-516 [Periódico revisado por pares]New York: John Wiley & Sons, IncTexto completo disponível |
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9 |
Material Type: Artigo
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Dissecting the Phenotype and Genotype of PLA2G6‐Related ParkinsonismMagrinelli, Francesca ; Mehta, Sahil ; Di Lazzaro, Giulia ; Latorre, Anna ; Edwards, Mark J. ; Balint, Bettina ; Basu, Purba ; Kobylecki, Christopher ; Groppa, Sergiu ; Hegde, Anaita ; Mulroy, Eoin ; Estevez‐Fraga, Carlos ; Arora, Anshita ; Kumar, Hrishikesh ; Schneider, Susanne A. ; Lewis, Patrick A. ; Jaunmuktane, Zane ; Revesz, Tamas ; Gandhi, Sonia ; Wood, Nicholas W. ; Hardy, John A. ; Tinazzi, Michele ; Lal, Vivek ; Houlden, Henry ; Bhatia, Kailash P.Movement disorders, 2022-01, Vol.37 (1), p.148-161 [Periódico revisado por pares]Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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10 |
Material Type: Artigo
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Behçet's disease and the nervous systemSERDAROGLU, PJournal of neurology, 1998-04, Vol.245 (4), p.197-205 [Periódico revisado por pares]Berlin: SpringerTexto completo disponível |