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A C Ludolph

Showing results (61-70 of 172) with videos related to

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Der Nervenarzt|February 21, 2020
[Gene-specific treatment approaches in amyotrophic lateral sclerosis in the present and future]D Brenner, A Freischmidt, A C Ludolph, et al.
Neurology|July 28, 2010
Novel missense and truncating mutations in FUS/TLS in familial ALSS Waibel, M Neumann, M Rabe, et al.
Neuroscience|January 1, 1995
Failure of neuronal ion exchange, not potentiated excitation, causes excitotoxicity after inhibition of oxidative phosphorylationM W Riepe, N Hori, A C Ludolph, et al.
Annals of Neurology|July 17, 1998
Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onsetT Gasser, K Windgassen, B Bereznai, et al.
European Journal of Neurology|August 28, 2007
Early diagnosis of rhinocerebral mucormycosis by cerebrospinal fluid analysis and determination of 16s rRNA gene sequenceD Bengel, M Susa, H Schreiber, et al.
EEG-EMG Zeitschrift Fur Elektroenzephalographie, Elektromyographie Und Verwandte Gebiete|March 1, 1987
[Methodology and normal values in recording evoked motor potentials following transcranial stimulation in the human]A C Ludolph, C E Elger, J H Gössling, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1997
Decreased N-acetyl-aspartate/choline ratio and increased lactate in the frontal lobe of patients with Huntington's disease: a proton magnetic resonance spectroscopy studyL Harms, H Meierkord, G Timm, et al.
Journal of Neurology|November 7, 2002
Transient Global Amnesia. Evidence against vascular ischemic etiology from diffusion weighted imagingR Huber, A J Aschoff, A C Ludolph, et al.
European Journal of Biochemistry|November 28, 2001
A novel calcineurin splice variant that modifies calcineurin activityA Reuter, J Mi, I Sehrsam, et al.
Acta Neurologica Scandinavica|March 1, 1991
Functional and morphological deficits in late-treated patients with homocystinuria: a clinical, electrophysiologic and MRI studyA C Ludolph, K Ullrich, U Bick, et al.
Pageof 18

Showing results (61-70 of 172) with videos related to

Sort By:
Pageof 18
Der Nervenarzt|February 21, 2020
[Gene-specific treatment approaches in amyotrophic lateral sclerosis in the present and future]D Brenner, A Freischmidt, A C Ludolph, et al.
Neurology|July 28, 2010
Novel missense and truncating mutations in FUS/TLS in familial ALSS Waibel, M Neumann, M Rabe, et al.
Neuroscience|January 1, 1995
Failure of neuronal ion exchange, not potentiated excitation, causes excitotoxicity after inhibition of oxidative phosphorylationM W Riepe, N Hori, A C Ludolph, et al.
Annals of Neurology|July 17, 1998
Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onsetT Gasser, K Windgassen, B Bereznai, et al.
European Journal of Neurology|August 28, 2007
Early diagnosis of rhinocerebral mucormycosis by cerebrospinal fluid analysis and determination of 16s rRNA gene sequenceD Bengel, M Susa, H Schreiber, et al.
EEG-EMG Zeitschrift Fur Elektroenzephalographie, Elektromyographie Und Verwandte Gebiete|March 1, 1987
[Methodology and normal values in recording evoked motor potentials following transcranial stimulation in the human]A C Ludolph, C E Elger, J H Gössling, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1997
Decreased N-acetyl-aspartate/choline ratio and increased lactate in the frontal lobe of patients with Huntington's disease: a proton magnetic resonance spectroscopy studyL Harms, H Meierkord, G Timm, et al.
Journal of Neurology|November 7, 2002
Transient Global Amnesia. Evidence against vascular ischemic etiology from diffusion weighted imagingR Huber, A J Aschoff, A C Ludolph, et al.
European Journal of Biochemistry|November 28, 2001
A novel calcineurin splice variant that modifies calcineurin activityA Reuter, J Mi, I Sehrsam, et al.
Acta Neurologica Scandinavica|March 1, 1991
Functional and morphological deficits in late-treated patients with homocystinuria: a clinical, electrophysiologic and MRI studyA C Ludolph, K Ullrich, U Bick, et al.
Pageof 18