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Saeed Bohlega

Showing results (1-10 of 64) with videos related to

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Neurology International|November 5, 2011
Novel mutation of the notch3 gene in arabic family with CADASILSaeed Bohlega
Neurology International|July 22, 2016
Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 MutationMohammed Alqwaifly, Saeed Bohlega
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2006
Unilateral pallidotomy for hemidystoniaAhmed Alkhani, Saeed Bohlega
American 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 Bohlega
Journal 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 Bohlega
BMJ Neurology Open|May 23, 2022
Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalationWalaa B Mohammed, Salma Tarabzouni, Saeed Bohlega
Tremor 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 Bohlega
Annals of Neurology|August 16, 2011
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosisAmr Al-Saif, Futwan Al-Mohanna, Saeed Bohlega
Annals of Neurology|October 31, 2012
Loss of ERLIN2 function leads to juvenile primary lateral sclerosisAmr Al-Saif, Saeed Bohlega, Futwan Al-Mohanna
European Journal of Human Genetics : EJHG|October 3, 2013
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissuesSaeed Bohlega, Huda Al-Ajlan, Amr Al-Saif
Pageof 7

Showing results (1-10 of 64) with videos related to

Sort By:
Pageof 7
Neurology International|November 5, 2011
Novel mutation of the notch3 gene in arabic family with CADASILSaeed Bohlega
Neurology International|July 22, 2016
Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 MutationMohammed Alqwaifly, Saeed Bohlega
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2006
Unilateral pallidotomy for hemidystoniaAhmed Alkhani, Saeed Bohlega
American 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 Bohlega
Journal 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 Bohlega
BMJ Neurology Open|May 23, 2022
Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalationWalaa B Mohammed, Salma Tarabzouni, Saeed Bohlega
Tremor 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 Bohlega
Annals of Neurology|August 16, 2011
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosisAmr Al-Saif, Futwan Al-Mohanna, Saeed Bohlega
Annals of Neurology|October 31, 2012
Loss of ERLIN2 function leads to juvenile primary lateral sclerosisAmr Al-Saif, Saeed Bohlega, Futwan Al-Mohanna
European Journal of Human Genetics : EJHG|October 3, 2013
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissuesSaeed Bohlega, Huda Al-Ajlan, Amr Al-Saif
Pageof 7