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European Journal of Neurology
|
May 23, 2014
Revisiting the spectrum of lower motor neuron diseases with snake eyes appearance on magnetic resonance imaging
M-V Lebouteux, J Franques, R Guillevin, et al.
Clinical Chemistry
|
July 1, 1996
Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12
A Vandenberghe, P Latour, G Chauplannaz, et al.
Neuromuscular Disorders : NMD
|
May 23, 2001
X-linked myopathy with excessive autophagy: a clinicopathological study of five new families
B Chabrol, D Figarella-Branger, M Coquet, et al.
Archives of Physical Medicine and Rehabilitation
|
July 7, 2009
Periodic salbutamol in facioscapulohumeral muscular dystrophy: a randomized controlled trial
C A Payan, J Y Hogrel, E H Hammouda, et al.
Neuroradiology
|
November 7, 1999
MRI of the intracranial corticospinal tracts in amyotrophic and primary lateral sclerosis
P Peretti-Viton, J P Azulay, S Trefouret, et al.
Neurology
|
June 1, 1992
31P NMR spectroscopy and ergometer exercise test as evidence for muscle oxidative performance improvement with coenzyme Q in mitochondrial myopathies
D Bendahan, C Desnuelle, D Vanuxem, et al.
Neuromuscular Disorders : NMD
|
December 4, 2001
Myopathy with lobulated muscle fibers: evidence for heterogeneous etiology and clinical presentation
D Figarella-Branger, M El-Dassouki, A Saenz, et al.
Journal of the Neurological Sciences
|
May 17, 2014
Primary neurolymphomatosis diagnosis and treatment: a retrospective study
S Lagarde, E Tabouret, M Matta, et al.
Neuromuscular Disorders : NMD
|
October 27, 2009
Immunolabelling and flow cytometry as new tools to explore dysferlinopathies
N Wein, M Krahn, S Courrier, et al.
Revue Neurologique
|
April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]
G Bassez, S Attarian, P Laforêt, et al.
Page
of 23
Search research articles
Search
Showing results (201-210 of 227) with videos related to
Sort By:
Page
of 23
European Journal of Neurology
|
May 23, 2014
Revisiting the spectrum of lower motor neuron diseases with snake eyes appearance on magnetic resonance imaging
M-V Lebouteux, J Franques, R Guillevin, et al.
Clinical Chemistry
|
July 1, 1996
Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12
A Vandenberghe, P Latour, G Chauplannaz, et al.
Neuromuscular Disorders : NMD
|
May 23, 2001
X-linked myopathy with excessive autophagy: a clinicopathological study of five new families
B Chabrol, D Figarella-Branger, M Coquet, et al.
Archives of Physical Medicine and Rehabilitation
|
July 7, 2009
Periodic salbutamol in facioscapulohumeral muscular dystrophy: a randomized controlled trial
C A Payan, J Y Hogrel, E H Hammouda, et al.
Neuroradiology
|
November 7, 1999
MRI of the intracranial corticospinal tracts in amyotrophic and primary lateral sclerosis
P Peretti-Viton, J P Azulay, S Trefouret, et al.
Neurology
|
June 1, 1992
31P NMR spectroscopy and ergometer exercise test as evidence for muscle oxidative performance improvement with coenzyme Q in mitochondrial myopathies
D Bendahan, C Desnuelle, D Vanuxem, et al.
Neuromuscular Disorders : NMD
|
December 4, 2001
Myopathy with lobulated muscle fibers: evidence for heterogeneous etiology and clinical presentation
D Figarella-Branger, M El-Dassouki, A Saenz, et al.
Journal of the Neurological Sciences
|
May 17, 2014
Primary neurolymphomatosis diagnosis and treatment: a retrospective study
S Lagarde, E Tabouret, M Matta, et al.
Neuromuscular Disorders : NMD
|
October 27, 2009
Immunolabelling and flow cytometry as new tools to explore dysferlinopathies
N Wein, M Krahn, S Courrier, et al.
Revue Neurologique
|
April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]
G Bassez, S Attarian, P Laforêt, et al.
Page
of 23