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Annales De Biologie Clinique
|
December 16, 2003
[Difficult diagnosis of autoimmune peripheral neuropathy]
L Limousin, J Neil, N Le Forestier, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 11, 2000
Sleep disorders and diaphragmatic function in patients with amyotrophic lateral sclerosis
I Arnulf, T Similowski, F Salachas, et al.
Brain : a Journal of Neurology
|
September 26, 2001
Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature
N Le Forestier, T Maisonobe, A Piquard, et al.
Journal of the Neurological Sciences
|
October 6, 2000
Blood oxidative stress in amyotrophic lateral sclerosis
D Bonnefont-Rousselot, L Lacomblez, M Jaudon, et al.
Supplements to Clinical Neurophysiology
|
August 19, 2010
Motor neuron disorders: novel electrophysiologic approach (MUFDEC protocol)
F C Wang, N Le Forestier, P Gérard, et al.
Revue Neurologique
|
January 1, 1984
[Methylation of erythrocyte membrane phospholipids: correlation with membrane viscosity. Study of normal and parkinsonian subjects]
V Meininger, T Phan, J C Camelin, et al.
Neurology
|
June 14, 2006
The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V
O Dubourg, H Azzedine, R Ben Yaou, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
Antiglycolipid antibodies in motor neuropathies
N Baumann, M L Harpin, Y Marie, et al.
The European Respiratory Journal
|
March 8, 2000
Diaphragmatic dysfunction and dyspnoea in amyotrophic lateral sclerosis
T Similowski, V Attali, G Bensimon, et al.
Neurology
|
April 10, 2002
APOE: a potential marker of disease progression in ALS
L Lacomblez, V Doppler, I Beucler, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 156) with videos related to
Sort By:
Page
of 16
Annales De Biologie Clinique
|
December 16, 2003
[Difficult diagnosis of autoimmune peripheral neuropathy]
L Limousin, J Neil, N Le Forestier, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 11, 2000
Sleep disorders and diaphragmatic function in patients with amyotrophic lateral sclerosis
I Arnulf, T Similowski, F Salachas, et al.
Brain : a Journal of Neurology
|
September 26, 2001
Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature
N Le Forestier, T Maisonobe, A Piquard, et al.
Journal of the Neurological Sciences
|
October 6, 2000
Blood oxidative stress in amyotrophic lateral sclerosis
D Bonnefont-Rousselot, L Lacomblez, M Jaudon, et al.
Supplements to Clinical Neurophysiology
|
August 19, 2010
Motor neuron disorders: novel electrophysiologic approach (MUFDEC protocol)
F C Wang, N Le Forestier, P Gérard, et al.
Revue Neurologique
|
January 1, 1984
[Methylation of erythrocyte membrane phospholipids: correlation with membrane viscosity. Study of normal and parkinsonian subjects]
V Meininger, T Phan, J C Camelin, et al.
Neurology
|
June 14, 2006
The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V
O Dubourg, H Azzedine, R Ben Yaou, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
Antiglycolipid antibodies in motor neuropathies
N Baumann, M L Harpin, Y Marie, et al.
The European Respiratory Journal
|
March 8, 2000
Diaphragmatic dysfunction and dyspnoea in amyotrophic lateral sclerosis
T Similowski, V Attali, G Bensimon, et al.
Neurology
|
April 10, 2002
APOE: a potential marker of disease progression in ALS
L Lacomblez, V Doppler, I Beucler, et al.
Page
of 16