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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 |
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Material Type: Artigo
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Cerebral manifestation of Erdheim-Chester disease : Clinical and radiologic findingsBOHLEGA, S ; ALWATBAN, J ; TULBAH, A ; BAKHEET, S. M ; POWE, JNeurology, 1997-12, Vol.49 (6), p.1702-1705 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsSem texto completo |
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Material Type: Artigo
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Gaucher disease with oculomotor apraxia and cardiovascular calcification (Gaucher type IIIC)BOHLEGA, S ; KAMBOURIS, M ; SHAHID, M ; AL HOMSI, M ; AL SOUS, WNeurology, 2000-01, Vol.54 (1), p.261-263 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsSem texto completo |
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Material Type: Artigo
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Neuroacanthocytosis and aprebetalipoproteinemiaBOHLEGA, S ; RILEY, W ; POWE, J ; BAYNTON, R ; ROBERTS, GNeurology, 1998-06, Vol.50 (6), p.1912-1914 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsSem texto completo |
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Material Type: Artigo
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The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxiaLORENZETTI, D ; BOHLEGA, S ; ZOGHBI, H. YNeurology, 1997-10, Vol.49 (4), p.1009-1013 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsSem texto completo |
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Material Type: Artigo
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MRI findings in neuro-Behçet's diseaseZUHEIR AL KAWI, M ; BOHLEGA, S ; BANNA, MNeurology, 1991-03, Vol.41 (3), p.405-408 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsSem texto completo |