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Der Nervenarzt
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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 ALS
S 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 phosphorylation
M 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 onset
T 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 sequence
D 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 study
L Harms, H Meierkord, G Timm, et al.
Journal of Neurology
|
November 7, 2002
Transient Global Amnesia. Evidence against vascular ischemic etiology from diffusion weighted imaging
R Huber, A J Aschoff, A C Ludolph, et al.
European Journal of Biochemistry
|
November 28, 2001
A novel calcineurin splice variant that modifies calcineurin activity
A 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 study
A C Ludolph, K Ullrich, U Bick, et al.
Page
of 18
Search research articles
Search
Showing results (61-70 of 172) with videos related to
Sort By:
Page
of 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 ALS
S 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 phosphorylation
M 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 onset
T 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 sequence
D 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 study
L Harms, H Meierkord, G Timm, et al.
Journal of Neurology
|
November 7, 2002
Transient Global Amnesia. Evidence against vascular ischemic etiology from diffusion weighted imaging
R Huber, A J Aschoff, A C Ludolph, et al.
European Journal of Biochemistry
|
November 28, 2001
A novel calcineurin splice variant that modifies calcineurin activity
A 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 study
A C Ludolph, K Ullrich, U Bick, et al.
Page
of 18