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F Stögbauer

Showing results (21-30 of 56) with videos related to

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Muscle & Nerve|August 14, 1998
Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 geneF Stögbauer, P Young, M Kerschensteiner, et al.
Cephalalgia : an International Journal of Headache|January 24, 2006
Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association studyS Schwaag, S Evers, A Schirmacher, et al.
Acta Neurologica Scandinavica|March 5, 2003
Spontaneous internal carotid artery dissection and alpha-1-antitrypsin deficiencyC Konrad, D G Nabavi, R Junker, et al.
Journal of Neurochemistry|August 11, 2000
Oncostatin M-mediated growth inhibition of human glioblastoma cells does not depend on stat3 or on mitogen-activated protein kinase activationH Halfter, F Stögbauer, M Friedrich, et al.
Journal of Neurochemistry|March 10, 2001
Complete inhibition of in vivo glioma growth by oncostatin MM Friedrich, N Höss, F Stögbauer, et al.
Cerebrovascular Diseases (Basel, Switzerland)|October 20, 2001
Clinically silent circulating microemboli in 20 patients with carotid or vertebral artery dissectionD W Droste, K Junker, F Stögbauer, et al.
Human Genetics|May 1, 1997
Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25F Stögbauer, P Young, V Timmerman, et al.
Journal of Neuro-Oncology|October 6, 1998
Growth inhibition of newly established human glioma cell lines by leukemia inhibitory factorH Halfter, J Kremerskothen, J Weber, et al.
Neurology|April 24, 2002
Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin geneG Kuhlenbäumer, P Young, C Oberwittler, et al.
Bioelectromagnetics|July 19, 2000
Electromagnetic fields (1.8 GHz) increase the permeability to sucrose of the blood-brain barrier in vitroA Schirmacher, S Winters, S Fischer, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Muscle & Nerve|August 14, 1998
Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 geneF Stögbauer, P Young, M Kerschensteiner, et al.
Cephalalgia : an International Journal of Headache|January 24, 2006
Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association studyS Schwaag, S Evers, A Schirmacher, et al.
Acta Neurologica Scandinavica|March 5, 2003
Spontaneous internal carotid artery dissection and alpha-1-antitrypsin deficiencyC Konrad, D G Nabavi, R Junker, et al.
Journal of Neurochemistry|August 11, 2000
Oncostatin M-mediated growth inhibition of human glioblastoma cells does not depend on stat3 or on mitogen-activated protein kinase activationH Halfter, F Stögbauer, M Friedrich, et al.
Journal of Neurochemistry|March 10, 2001
Complete inhibition of in vivo glioma growth by oncostatin MM Friedrich, N Höss, F Stögbauer, et al.
Cerebrovascular Diseases (Basel, Switzerland)|October 20, 2001
Clinically silent circulating microemboli in 20 patients with carotid or vertebral artery dissectionD W Droste, K Junker, F Stögbauer, et al.
Human Genetics|May 1, 1997
Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25F Stögbauer, P Young, V Timmerman, et al.
Journal of Neuro-Oncology|October 6, 1998
Growth inhibition of newly established human glioma cell lines by leukemia inhibitory factorH Halfter, J Kremerskothen, J Weber, et al.
Neurology|April 24, 2002
Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin geneG Kuhlenbäumer, P Young, C Oberwittler, et al.
Bioelectromagnetics|July 19, 2000
Electromagnetic fields (1.8 GHz) increase the permeability to sucrose of the blood-brain barrier in vitroA Schirmacher, S Winters, S Fischer, et al.
Pageof 6