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BMJ Case Reports
|
June 21, 2011
Hypocretinergic dysfunction in neuromyelitis optica with coma-like episodes
B Carlander, T Vincent, A Le Floch, et al.
La Revue De Medecine Interne
|
August 18, 2001
[Acute motor axonal neuropathy and aseptic meningitis due to Staphylococcus aureus endocarditis]
P Corne, P Massanet, L Amigues, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 19, 2008
Hypocretinergic dysfunction in neuromyelitis optica with coma-like episodes
B Carlander, T Vincent, A Le Floch, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Motoneuron survival factors: biological roles and therapeutic potential
C E Henderson, E Bloch-Gallego, W Camu, et al.
Annals of Neurology
|
May 19, 1998
Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease
B Moulard, F Salachas, B Chassande, et al.
Journal of the Neurological Sciences
|
July 3, 2021
An amyotrophic lateral sclerosis hot spot in the French Alps associated with genotoxic fungi
E Lagrange, J P Vernoux, J Reis, et al.
Journal of the Neurological Sciences
|
August 17, 1999
Genetics of familial ALS and consequences for diagnosis. French ALS Research Group
W Camu, J Khoris, B Moulard, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
August 1, 1995
Embryonic rat motoneurons express a functional P-type voltage-dependent calcium channel
B Hivert, S Bouhanna, S Diochot, et al.
Revue Neurologique
|
January 1, 1994
[Somatosensory evoked potentials in amyotrophic lateral sclerosis and primary lateral sclerosis]
M Georgesco, A Salerno, B Carlander, et al.
Revue Neurologique
|
February 24, 2004
[Superoxyde dismutase 1 gene abnormalities in familial amyotrophic lateral sclerosis: phenotype/genotype correlations. The French experience and review of the literature]
H F Jafari-Schluep, J Khoris, V Mayeux-Portas, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 83) with videos related to
Sort By:
Page
of 9
BMJ Case Reports
|
June 21, 2011
Hypocretinergic dysfunction in neuromyelitis optica with coma-like episodes
B Carlander, T Vincent, A Le Floch, et al.
La Revue De Medecine Interne
|
August 18, 2001
[Acute motor axonal neuropathy and aseptic meningitis due to Staphylococcus aureus endocarditis]
P Corne, P Massanet, L Amigues, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 19, 2008
Hypocretinergic dysfunction in neuromyelitis optica with coma-like episodes
B Carlander, T Vincent, A Le Floch, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Motoneuron survival factors: biological roles and therapeutic potential
C E Henderson, E Bloch-Gallego, W Camu, et al.
Annals of Neurology
|
May 19, 1998
Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease
B Moulard, F Salachas, B Chassande, et al.
Journal of the Neurological Sciences
|
July 3, 2021
An amyotrophic lateral sclerosis hot spot in the French Alps associated with genotoxic fungi
E Lagrange, J P Vernoux, J Reis, et al.
Journal of the Neurological Sciences
|
August 17, 1999
Genetics of familial ALS and consequences for diagnosis. French ALS Research Group
W Camu, J Khoris, B Moulard, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
August 1, 1995
Embryonic rat motoneurons express a functional P-type voltage-dependent calcium channel
B Hivert, S Bouhanna, S Diochot, et al.
Revue Neurologique
|
January 1, 1994
[Somatosensory evoked potentials in amyotrophic lateral sclerosis and primary lateral sclerosis]
M Georgesco, A Salerno, B Carlander, et al.
Revue Neurologique
|
February 24, 2004
[Superoxyde dismutase 1 gene abnormalities in familial amyotrophic lateral sclerosis: phenotype/genotype correlations. The French experience and review of the literature]
H F Jafari-Schluep, J Khoris, V Mayeux-Portas, et al.
Page
of 9