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Clinical patterns of neurological involvement in Behçet's disease : evaluation of 200 patientsAKMAN-DEMIR, G ; SERDAROGLU, P ; TASCI, BBrain (London, England : 1878), 1999-11, Vol.122 (11), p.2171-2181 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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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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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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Material Type: Artigo
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Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1Al-Semari, Abdulaziz ; Bohlega, SaeedAmerican journal of medical genetics. Part A, 2007-01, Vol.143A (2), p.149-160 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Neurobrucellosis: Clinical and neuroimaging correlationAL-SOUS, M. Walid ; BOHLEGA, Saeed ; AL-KAWI, M. Zuheir ; ALWATBAN, Jehad ; MCLEAN, Donald RAmerican journal of neuroradiology : AJNR, 2004-03, Vol.25 (3), p.395-401 [Periódico revisado por pares]Oak Brook, IL: American Society of NeuroradiologyTexto completo disponível |
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Material Type: Artigo
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Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extra pyramidal SyndromeALAZAMI, Anas M ; AL-SAIF, Amr ; BALTUS, Andy ; PETERLIN, Borut ; DANDA, Sumita ; BHATIA, Kailash P ; SCHNEIDER, Susanne A ; SAKATI, Nadia ; WALSH, Christopher A ; AL-MOHANNA, Futwan ; MEYER, Brian ; ALKURAYA, Fowzan S ; AL-SEMARI, Abdulaziz ; BOHLEGA, Saeed ; ZLITNI, Soumaya ; ALZAHRANI, Fatema ; BAVI, Prashant ; KAYA, Namik ; COLAK, Dilek ; KHALAK, HanifAmerican journal of human genetics, 2008, Vol.83 (6), p.684-691 [Periódico revisado por pares]Cambridge, MA: Cell PressTexto completo disponível |
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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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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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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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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 |