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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 cytopathy
W 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 disease
G 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 defect
P 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 patients
A 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 nucleus
T Hummel, U Jahnke, U Sommer, et al.
Journal of Neurology
|
September 2, 2008
Transient neonatal Lambert-Eaton syndrome
U Reuner, G Kamin, G Ramantani, et al.
Journal of Neurochemistry
|
May 1, 1991
Mitochondrial DNA in postmortem brain from patients with Parkinson's disease
P Lestienne, I Nelson, P Riederer, et al.
Neurology
|
November 26, 2009
Education research: cognitive performance is preserved in sleep-deprived neurology residents
M 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 dystrophy
R 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 family
F R Kreuz, T Grünewald, A Müller, et al.
Page
of 28
Search research articles
Search
Showing results (131-140 of 273) with videos related to
Sort By:
Page
of 28
Intensive Care Medicine
|
November 1, 1994
A case of myoclonus epilepsy and lactic acidosis: difficulties in diagnosis and treatment of terminal mitochondrial cytopathy
W 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 disease
G 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 defect
P 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 patients
A 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 nucleus
T Hummel, U Jahnke, U Sommer, et al.
Journal of Neurology
|
September 2, 2008
Transient neonatal Lambert-Eaton syndrome
U Reuner, G Kamin, G Ramantani, et al.
Journal of Neurochemistry
|
May 1, 1991
Mitochondrial DNA in postmortem brain from patients with Parkinson's disease
P Lestienne, I Nelson, P Riederer, et al.
Neurology
|
November 26, 2009
Education research: cognitive performance is preserved in sleep-deprived neurology residents
M 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 dystrophy
R 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 family
F R Kreuz, T Grünewald, A Müller, et al.
Page
of 28