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H Reichmann

Showing results (141-150 of 273) with videos related to

Pageof 28
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Lancet (London, England)|February 16, 1999
Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositisJ Lampe, H Kitzler, M C Walter, et al.
Der Nervenarzt|June 29, 2004
[Attitudes towards patient care at the end of life. A survey of directors of neurological departments]G D Borasio, B Weltermann, R Voltz, et al.
Der Nervenarzt|June 1, 1991
[Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations]R Gold, W Kress, B Meurers, et al.
Der Nervenarzt|September 24, 2002
[Pramipexole in Parkinson disease. Results of a treatment observation]H Reichmann, H M Brecht, P H Kraus, et al.
Neurology|March 29, 2001
Modafinil for excessive daytime sleepiness in myotonic dystrophyM S Damian, A Gerlach, F Schmidt, et al.
Lancet (London, England)|February 13, 1993
Mitochondrial gene mutations and diabetes mellitusJ B Schulz, T Klockgether, J Dichgans, et al.
Cerebrovascular Diseases (Basel, Switzerland)|September 4, 1999
Noninvasive assessment of the circle of Willis in cerebral ischemia: the potential of CT angiography and contrast-enhanced transcranial color-coded duplexsonographyG Gahn, J Gerber, S Hallmeyer, et al.
Fortschritte Der Neurologie-Psychiatrie|May 31, 2008
[Parainfectious polyneuropathy and miller-fisher-syndrome in combination with anemia in Mycoplasma pneumoniae infection]K F Loewenbrück, V Pütz, J Schäfer, et al.
Folia Neuropathologica|April 25, 2015
Cabergoline protects dopaminergic neurons against rotenone-induced cell death in primary mesencephalic cell cultureJ Meinel, K Radad, W-D Rausch, et al.
Journal of the Neurological Sciences|September 25, 2009
Immunohistochemical, volumetric, and functional neuroimaging studies in patients with idiopathic Parkinson's diseaseT Hummel, M Witt, H Reichmann, et al.
Pageof 28

Showing results (141-150 of 273) with videos related to

Sort By:
Pageof 28
Lancet (London, England)|February 16, 1999
Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositisJ Lampe, H Kitzler, M C Walter, et al.
Der Nervenarzt|June 29, 2004
[Attitudes towards patient care at the end of life. A survey of directors of neurological departments]G D Borasio, B Weltermann, R Voltz, et al.
Der Nervenarzt|June 1, 1991
[Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations]R Gold, W Kress, B Meurers, et al.
Der Nervenarzt|September 24, 2002
[Pramipexole in Parkinson disease. Results of a treatment observation]H Reichmann, H M Brecht, P H Kraus, et al.
Neurology|March 29, 2001
Modafinil for excessive daytime sleepiness in myotonic dystrophyM S Damian, A Gerlach, F Schmidt, et al.
Lancet (London, England)|February 13, 1993
Mitochondrial gene mutations and diabetes mellitusJ B Schulz, T Klockgether, J Dichgans, et al.
Cerebrovascular Diseases (Basel, Switzerland)|September 4, 1999
Noninvasive assessment of the circle of Willis in cerebral ischemia: the potential of CT angiography and contrast-enhanced transcranial color-coded duplexsonographyG Gahn, J Gerber, S Hallmeyer, et al.
Fortschritte Der Neurologie-Psychiatrie|May 31, 2008
[Parainfectious polyneuropathy and miller-fisher-syndrome in combination with anemia in Mycoplasma pneumoniae infection]K F Loewenbrück, V Pütz, J Schäfer, et al.
Folia Neuropathologica|April 25, 2015
Cabergoline protects dopaminergic neurons against rotenone-induced cell death in primary mesencephalic cell cultureJ Meinel, K Radad, W-D Rausch, et al.
Journal of the Neurological Sciences|September 25, 2009
Immunohistochemical, volumetric, and functional neuroimaging studies in patients with idiopathic Parkinson's diseaseT Hummel, M Witt, H Reichmann, et al.
Pageof 28