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Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2006
Unilateral pallidotomy for hemidystoniaAhmed Alkhani, Saeed BohlegaNeurology International|November 5, 2011
Novel mutation of the notch3 gene in arabic family with CADASILSaeed BohlegaNeurology International|July 22, 2016
Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 MutationMohammed Alqwaifly, Saeed BohlegaAmerican Journal of Medical Genetics. Part A|December 15, 2006
Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1Abdulaziz Al-Semari, Saeed BohlegaJournal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 8, 2021
Multimodal Evoked Potential Profiles in Woodhouse-Sakati SyndromeAli Abusrair, Iftetah AlHamoud, Saeed BohlegaChild'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 22, 2005
Colloid cysts in children, a clinical and radiological studyNabeel Alnaghmoosh, Ahmed AlkhaniBMJ Neurology Open|May 23, 2022
Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalationWalaa B Mohammed, Salma Tarabzouni, Saeed BohlegaTremor and Other Hyperkinetic Movements (New York, N.Y.)|October 10, 2022
Tremor in Parkinson's Disease: From Pathophysiology to Advanced TherapiesAli H Abusrair, Walaa Elsekaily, Saeed BohlegaAnnals of Neurology|August 16, 2011
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosisAmr Al-Saif, Futwan Al-Mohanna, Saeed BohlegaAnnals of Neurology|October 31, 2012
Loss of ERLIN2 function leads to juvenile primary lateral sclerosisAmr Al-Saif, Saeed Bohlega, Futwan Al-MohannaPageof 10