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Claude Desnuelle

Showing results (51-60 of 74) with videos related to

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Journal of the Neurological Sciences|January 27, 2016
Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathiesJean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
Neuromuscular Disorders : NMD|April 23, 2016
Unusual association of amyotrophic lateral sclerosis and myasthenia gravis: A dysregulation of the adaptive immune system?Maria Del Mar Amador, Nadia Vandenberghe, Nawel Berhoune, et al.
Stem Cells (Dayton, Ohio)|February 6, 2010
Isolation of a highly myogenic CD34-negative subset of human skeletal muscle cells free of adipogenic potentialDidier F Pisani, Claude A Dechesne, Sabrina Sacconi, et al.
Human Molecular Genetics|August 23, 2013
DUX4 and DUX4 downstream target genes are expressed in fetal FSHD musclesMaxime Ferreboeuf, Virginie Mariot, Bettina Bessières, et al.
Human Molecular Genetics|March 14, 2008
A functionally dominant mitochondrial DNA mutationSabrina Sacconi, Leonardo Salviati, Yutaka Nishigaki, et al.
Human Mutation|February 7, 2008
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with coresNicole Monnier, Isabelle Marty, Julien Faure, et al.
Annals of Neurology|May 29, 2015
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophyVirginie Mariot, Stephane Roche, Christophe Hourdé, et al.
Human Molecular Genetics|June 20, 2013
Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophyNatacha Broucqsault, Julia Morere, Marie-Cécile Gaillard, et al.
Biomed Research International|May 9, 2018
Safety of Intravenous Immunoglobulin (Tegeline®), Administered at Home in Patients with Autoimmune Disease: Results of a French StudyEric Hachulla, Gwendal Le Masson, Guilhem Solé, et al.
The Lancet. Neurology|October 19, 2016
Early diaphragm pacing in patients with amyotrophic lateral sclerosis (RespiStimALS): a randomised controlled triple-blind trialJésus Gonzalez-Bermejo, Capucine Morélot-Panzini, Marie-Laure Tanguy, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Journal of the Neurological Sciences|January 27, 2016
Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathiesJean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
Neuromuscular Disorders : NMD|April 23, 2016
Unusual association of amyotrophic lateral sclerosis and myasthenia gravis: A dysregulation of the adaptive immune system?Maria Del Mar Amador, Nadia Vandenberghe, Nawel Berhoune, et al.
Stem Cells (Dayton, Ohio)|February 6, 2010
Isolation of a highly myogenic CD34-negative subset of human skeletal muscle cells free of adipogenic potentialDidier F Pisani, Claude A Dechesne, Sabrina Sacconi, et al.
Human Molecular Genetics|August 23, 2013
DUX4 and DUX4 downstream target genes are expressed in fetal FSHD musclesMaxime Ferreboeuf, Virginie Mariot, Bettina Bessières, et al.
Human Molecular Genetics|March 14, 2008
A functionally dominant mitochondrial DNA mutationSabrina Sacconi, Leonardo Salviati, Yutaka Nishigaki, et al.
Human Mutation|February 7, 2008
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with coresNicole Monnier, Isabelle Marty, Julien Faure, et al.
Annals of Neurology|May 29, 2015
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophyVirginie Mariot, Stephane Roche, Christophe Hourdé, et al.
Human Molecular Genetics|June 20, 2013
Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophyNatacha Broucqsault, Julia Morere, Marie-Cécile Gaillard, et al.
Biomed Research International|May 9, 2018
Safety of Intravenous Immunoglobulin (Tegeline®), Administered at Home in Patients with Autoimmune Disease: Results of a French StudyEric Hachulla, Gwendal Le Masson, Guilhem Solé, et al.
The Lancet. Neurology|October 19, 2016
Early diaphragm pacing in patients with amyotrophic lateral sclerosis (RespiStimALS): a randomised controlled triple-blind trialJésus Gonzalez-Bermejo, Capucine Morélot-Panzini, Marie-Laure Tanguy, et al.
Pageof 8