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H Reichmann

Showing results (131-140 of 273) with videos related to

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Intensive Care Medicine|November 1, 1994
A case of myoclonus epilepsy and lactic acidosis: difficulties in diagnosis and treatment of terminal mitochondrial cytopathyW Müllges, T Dorn, W Paulus, et al.
Annals of the New York Academy of Sciences|July 9, 2004
Oxidative stress to dopaminergic neurons as models of Parkinson's diseaseG Gille, S-T Hung, H Reichmann, et al.
Journal of Neurochemistry|November 1, 1990
Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defectP Lestienne, J Nelson, P Riederer, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Clinical, morphological, biochemical, and neuroradiological features of mitochondrial encephalomyopathies. Presentation of 19 patientsA Lindner, E Hofmann, M Naumann, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 2, 2004
Olfactory function in patients with idiopathic Parkinson's disease: effects of deep brain stimulation in the subthalamic nucleusT Hummel, U Jahnke, U Sommer, et al.
Journal of Neurology|September 2, 2008
Transient neonatal Lambert-Eaton syndromeU Reuner, G Kamin, G Ramantani, et al.
Journal of Neurochemistry|May 1, 1991
Mitochondrial DNA in postmortem brain from patients with Parkinson's diseaseP Lestienne, I Nelson, P Riederer, et al.
Neurology|November 26, 2009
Education research: cognitive performance is preserved in sleep-deprived neurology residentsM Reimann, R Manz, S Prieur, et al.
Journal of Neurology|March 1, 1994
A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophyR Gold, W Kress, T Bettecken, et al.
Journal of Neurology|January 13, 2000
Spinocerebellar ataxia type 7: frequency of CAG repeat length in a German familyF R Kreuz, T Grünewald, A Müller, et al.
Pageof 28

Showing results (131-140 of 273) with videos related to

Sort By:
Pageof 28
Intensive Care Medicine|November 1, 1994
A case of myoclonus epilepsy and lactic acidosis: difficulties in diagnosis and treatment of terminal mitochondrial cytopathyW Müllges, T Dorn, W Paulus, et al.
Annals of the New York Academy of Sciences|July 9, 2004
Oxidative stress to dopaminergic neurons as models of Parkinson's diseaseG Gille, S-T Hung, H Reichmann, et al.
Journal of Neurochemistry|November 1, 1990
Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defectP Lestienne, J Nelson, P Riederer, et al.
Molecular and Cellular Biochemistry|October 6, 1997
Clinical, morphological, biochemical, and neuroradiological features of mitochondrial encephalomyopathies. Presentation of 19 patientsA Lindner, E Hofmann, M Naumann, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 2, 2004
Olfactory function in patients with idiopathic Parkinson's disease: effects of deep brain stimulation in the subthalamic nucleusT Hummel, U Jahnke, U Sommer, et al.
Journal of Neurology|September 2, 2008
Transient neonatal Lambert-Eaton syndromeU Reuner, G Kamin, G Ramantani, et al.
Journal of Neurochemistry|May 1, 1991
Mitochondrial DNA in postmortem brain from patients with Parkinson's diseaseP Lestienne, I Nelson, P Riederer, et al.
Neurology|November 26, 2009
Education research: cognitive performance is preserved in sleep-deprived neurology residentsM Reimann, R Manz, S Prieur, et al.
Journal of Neurology|March 1, 1994
A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophyR Gold, W Kress, T Bettecken, et al.
Journal of Neurology|January 13, 2000
Spinocerebellar ataxia type 7: frequency of CAG repeat length in a German familyF R Kreuz, T Grünewald, A Müller, et al.
Pageof 28