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A C Ludolph

Showing results (81-90 of 146) with videos related to

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Journal of Neurology|December 29, 2000
Recessively inherited amyotrophic lateral sclerosis: a Germany family with the D90A CuZn-SOD mutationS M Winter, A Claus, C Oberwittler, et al.
Acta Neurologica Scandinavica|December 1, 1993
Studies of the etiology and pathogenesis of motor neuron diseases. III. Magnetic cortical stimulation in patients with lathyrismJ Hugon, A C Ludolph, P S Spencer, et al.
Fortschritte Der Neurologie-Psychiatrie|May 31, 2012
[Inclusion body myositis, Paget's disease of the bone and frontotemporal dementia: early involvement of the heart and respiratory muscles]M Ponfick, A C Ludolph, G Dekomien, et al.
Journal of Neurology|February 22, 2018
In vivo assessment of retinal vessel pathology in amyotrophic lateral sclerosisA Abdelhak, A Hübers, K Böhm, et al.
Brain : a Journal of Neurology|April 19, 2002
Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2A D Sperfeld, C Hein, J M Schröder, et al.
Experimental Neurology|March 1, 1996
Mitochondrial oxidation in rat hippocampus can be preconditioned by selective chemical inhibition of succinic dehydrogenaseM W Riepe, W N Niemi, D Megow, et al.
Brain : a Journal of Neurology|February 1, 1987
Studies on the aetiology and pathogenesis of motor neuron diseases. 1. Lathyrism: clinical findings in established casesA C Ludolph, J Hugon, M P Dwivedi, et al.
Muscle & Nerve|April 1, 1988
A clinical neurophysiologic study of tropical spastic paraparesisA C Ludolph, J Hugon, G C Román, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 19, 2001
Impaired RNA splicing of 5'-regulatory sequences of the astroglial glutamate transporter EAAT2 in human astrocytomaC Münch, A Penndorf, B Schwalenstöcker, et al.
European Neurology|January 1, 1988
Chronic ergotamine abuse: evidence of functional impairment of long ascending spinal tractsA C Ludolph, I W Husstedt, H P Schlake, et al.
Pageof 15

Showing results (81-90 of 146) with videos related to

Sort By:
Pageof 15
Journal of Neurology|December 29, 2000
Recessively inherited amyotrophic lateral sclerosis: a Germany family with the D90A CuZn-SOD mutationS M Winter, A Claus, C Oberwittler, et al.
Acta Neurologica Scandinavica|December 1, 1993
Studies of the etiology and pathogenesis of motor neuron diseases. III. Magnetic cortical stimulation in patients with lathyrismJ Hugon, A C Ludolph, P S Spencer, et al.
Fortschritte Der Neurologie-Psychiatrie|May 31, 2012
[Inclusion body myositis, Paget's disease of the bone and frontotemporal dementia: early involvement of the heart and respiratory muscles]M Ponfick, A C Ludolph, G Dekomien, et al.
Journal of Neurology|February 22, 2018
In vivo assessment of retinal vessel pathology in amyotrophic lateral sclerosisA Abdelhak, A Hübers, K Böhm, et al.
Brain : a Journal of Neurology|April 19, 2002
Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2A D Sperfeld, C Hein, J M Schröder, et al.
Experimental Neurology|March 1, 1996
Mitochondrial oxidation in rat hippocampus can be preconditioned by selective chemical inhibition of succinic dehydrogenaseM W Riepe, W N Niemi, D Megow, et al.
Brain : a Journal of Neurology|February 1, 1987
Studies on the aetiology and pathogenesis of motor neuron diseases. 1. Lathyrism: clinical findings in established casesA C Ludolph, J Hugon, M P Dwivedi, et al.
Muscle & Nerve|April 1, 1988
A clinical neurophysiologic study of tropical spastic paraparesisA C Ludolph, J Hugon, G C Román, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 19, 2001
Impaired RNA splicing of 5'-regulatory sequences of the astroglial glutamate transporter EAAT2 in human astrocytomaC Münch, A Penndorf, B Schwalenstöcker, et al.
European Neurology|January 1, 1988
Chronic ergotamine abuse: evidence of functional impairment of long ascending spinal tractsA C Ludolph, I W Husstedt, H P Schlake, et al.
Pageof 15