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S Bohlega

Showing results (41-50 of 54) with videos related to

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Human Molecular Genetics|October 1, 1994
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersA Hentati, M A Pericak-Vance, F Lennon, et al.
American Journal of Human Genetics|June 23, 1998
Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked regionA C Jones, Y Yamamura, L Almasy, et al.
Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association|April 7, 2015
Effect of public knowledge, attitudes, and behavior on willingness to undergo colorectal cancer screening using the health belief modelMajid A Almadi, Mahmoud H Mosli, Mohamed S Bohlega, et al.
European Journal of Neurology|January 20, 2006
A recommended treatment algorithm in relapsing multiple sclerosis: report of an international consensus meetingD Karussis, L D Biermann, S Bohlega, et al.
Parkinsonism & Related Disorders|April 13, 2019
Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disordersSaeed A Bohlega, Hussam Abou-Al-Shaar, Amaal AlDakheel, et al.
Current Medical Research and Opinion|March 22, 2013
Consensus guidelines for the diagnosis and treatment of multiple sclerosisB Yamout, R Alroughani, M Al-Jumah, et al.
Current Medical Research and Opinion|May 7, 2015
Consensus recommendations for the diagnosis and treatment of multiple sclerosis: the Middle East North Africa Committee for Treatment and Research In Multiple Sclerosis (MENACTRIMS)B Yamout, R Alroughani, M Al-Jumah, et al.
Annals of Neurology|February 16, 1999
Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsyB A Minassian, J Sainz, J M Serratosa, et al.
Multiple Sclerosis and Related Disorders|November 1, 2019
Consensus recommendations for the diagnosis and treatment of multiple sclerosis: 2019 revisions to the MENACTRIMS guidelinesB Yamout, M Sahraian, S Bohlega, et al.
Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|October 1, 1994
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersA Hentati, M A Pericak-Vance, F Lennon, et al.
American Journal of Human Genetics|June 23, 1998
Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked regionA C Jones, Y Yamamura, L Almasy, et al.
Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association|April 7, 2015
Effect of public knowledge, attitudes, and behavior on willingness to undergo colorectal cancer screening using the health belief modelMajid A Almadi, Mahmoud H Mosli, Mohamed S Bohlega, et al.
European Journal of Neurology|January 20, 2006
A recommended treatment algorithm in relapsing multiple sclerosis: report of an international consensus meetingD Karussis, L D Biermann, S Bohlega, et al.
Parkinsonism & Related Disorders|April 13, 2019
Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disordersSaeed A Bohlega, Hussam Abou-Al-Shaar, Amaal AlDakheel, et al.
Current Medical Research and Opinion|March 22, 2013
Consensus guidelines for the diagnosis and treatment of multiple sclerosisB Yamout, R Alroughani, M Al-Jumah, et al.
Current Medical Research and Opinion|May 7, 2015
Consensus recommendations for the diagnosis and treatment of multiple sclerosis: the Middle East North Africa Committee for Treatment and Research In Multiple Sclerosis (MENACTRIMS)B Yamout, R Alroughani, M Al-Jumah, et al.
Annals of Neurology|February 16, 1999
Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsyB A Minassian, J Sainz, J M Serratosa, et al.
Multiple Sclerosis and Related Disorders|November 1, 2019
Consensus recommendations for the diagnosis and treatment of multiple sclerosis: 2019 revisions to the MENACTRIMS guidelinesB Yamout, M Sahraian, S Bohlega, et al.
Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.
Pageof 6