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Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
November 16, 2010
Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: a French national survey
Maya Abdelnour-Mallet, Annie Verschueren, Nathalie Guy, et al.
Muscle & Nerve
|
March 4, 2017
Genetic Characterization of a French Cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencing
Mathieu Cerino, Svetlana Gorokhova, Pascal Laforet, et al.
Journal of the Neurological Sciences
|
January 27, 2016
Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathies
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
Journal of Neurology
|
August 11, 2014
Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
European Journal of Human Genetics : EJHG
|
April 28, 2006
Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay
Mourad Naïmi, Sylvie Bannwarth, Vincent Procaccio, et al.
JAMA Neurology
|
August 5, 2014
Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study
Mathilde Renaud, Mathieu Anheim, Erik-Jan Kamsteeg, et al.
Molecular Neurobiology
|
November 1, 2016
Targeted Next-Generation Sequencing Reveals Novel TTN Mutations Causing Recessive Distal Titinopathy
Anni Evilä, Johanna Palmio, Anna Vihola, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 19, 2015
Improving molecular diagnosis of distal myopathies by targeted next-generation sequencing
Amandine Sevy, Mathieu Cerino, Svetlana Gorokhova, et al.
Human Molecular Genetics
|
October 22, 2004
MUSK, a new target for mutations causing congenital myasthenic syndrome
Frédéric Chevessier, Brice Faraut, Aymeric Ravel-Chapuis, et al.
Journal De La Societe De Biologie
|
August 24, 2005
[Pathophysiological characterization of congenital myasthenic syndromes: the example of mutations in the MUSK gene]
Frédéric Chevessier, Brice Faraut, Aymeric Ravel-Chapuis, et al.
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of 12
Search research articles
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Showing results (71-80 of 113) with videos related to
Sort By:
Page
of 12
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
November 16, 2010
Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: a French national survey
Maya Abdelnour-Mallet, Annie Verschueren, Nathalie Guy, et al.
Muscle & Nerve
|
March 4, 2017
Genetic Characterization of a French Cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencing
Mathieu Cerino, Svetlana Gorokhova, Pascal Laforet, et al.
Journal of the Neurological Sciences
|
January 27, 2016
Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathies
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
Journal of Neurology
|
August 11, 2014
Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
European Journal of Human Genetics : EJHG
|
April 28, 2006
Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay
Mourad Naïmi, Sylvie Bannwarth, Vincent Procaccio, et al.
JAMA Neurology
|
August 5, 2014
Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study
Mathilde Renaud, Mathieu Anheim, Erik-Jan Kamsteeg, et al.
Molecular Neurobiology
|
November 1, 2016
Targeted Next-Generation Sequencing Reveals Novel TTN Mutations Causing Recessive Distal Titinopathy
Anni Evilä, Johanna Palmio, Anna Vihola, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 19, 2015
Improving molecular diagnosis of distal myopathies by targeted next-generation sequencing
Amandine Sevy, Mathieu Cerino, Svetlana Gorokhova, et al.
Human Molecular Genetics
|
October 22, 2004
MUSK, a new target for mutations causing congenital myasthenic syndrome
Frédéric Chevessier, Brice Faraut, Aymeric Ravel-Chapuis, et al.
Journal De La Societe De Biologie
|
August 24, 2005
[Pathophysiological characterization of congenital myasthenic syndromes: the example of mutations in the MUSK gene]
Frédéric Chevessier, Brice Faraut, Aymeric Ravel-Chapuis, et al.
Page
of 12