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S Bohlega

Showing results (21-30 of 54) with videos related to

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Neuromuscular Disorders : NMD|July 23, 1998
Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological featuresE J Cupler, S Bohlega, R Hessler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1995
Multiphasic disseminated encephalomyelitis presenting as alternating hemiplegiaS Khan, B A Yaqub, C M Poser, et al.
Clinical Rheumatology|March 1, 1993
Association of anti-cardiolipin antibodies with vascular thrombosis and neurological manifestation of Behçets diseaseA N al-Dalaan, S R al-Ballaa, M A al-Janadi, et al.
Neurology|October 22, 1998
Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotypeC S Benton, R de Silva, S L Rutledge, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1995
Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imagingS Bohlega, B Stigsby, M Z al-Kawi, et al.
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.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Neuromuscular Disorders : NMD|July 23, 1998
Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological featuresE J Cupler, S Bohlega, R Hessler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1995
Multiphasic disseminated encephalomyelitis presenting as alternating hemiplegiaS Khan, B A Yaqub, C M Poser, et al.
Clinical Rheumatology|March 1, 1993
Association of anti-cardiolipin antibodies with vascular thrombosis and neurological manifestation of Behçets diseaseA N al-Dalaan, S R al-Ballaa, M A al-Janadi, et al.
Neurology|October 22, 1998
Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotypeC S Benton, R de Silva, S L Rutledge, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1995
Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imagingS Bohlega, B Stigsby, M Z al-Kawi, et al.
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.
Pageof 6