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Saudi Medical Journal|September 9, 2016
A novel autosomal recessive "Huntington's disease-like" neurodegenerative disorder in a Saudi familyA Y Al-Tahan, M P Divakaran, M Kambouris, et al.Neuromuscular Disorders : NMD|October 27, 2009
Novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia and multisystem failureS Bohlega, G Van Goethem, A Al Semari, et al.Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|October 1, 1995
Acute Wernicke's encephalopathy associated with hyperemesis gravidarum: magnetic resonance imaging findingsS M Omer, M Z al Kawi, J al Watban, et al.Cancer|June 15, 1994
Myelopathy after intrathecal chemotherapy. A case report with unique magnetic resonance imaging changesD R McLean, H M Clink, P Ernst, et al.Neurology|December 25, 2002
A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14C A Hodgkinson, S Bohlega, S N Abu-Amero, et al.The Journal of International Medical Research|June 3, 2010
Guidelines for the pharmacological treatment of peripheral neuropathic pain: expert panel recommendations for the middle East regionS Bohlega, T Alsaadi, A Amir, et al.AJNR. American Journal of Neuroradiology|November 10, 2018
Brain MR Imaging Findings in Woodhouse-Sakati SyndromeA H Abusrair, S Bohlega, A Al-Semari, et al.Neurology|December 10, 2003
Autosomal dominant hyaline body myopathy: clinical variability and pathologic findingsS Bohlega, B Lach, B F Meyer, et al.International Journal of Immunogenetics|June 4, 2009
HLA class I and class II polymorphisms in Saudi patients with myasthenia gravisA H Hajeer, F Al Sawidan, S Bohlega, et al.The Journal of Rheumatology|April 1, 1994
Behçet's disease in Saudi ArabiaA N al-Dalaan, S R al Balaa, K el Ramahi, et al.Pageof 7