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Stem Cells and Development
|
November 18, 2015
Modeling Andersen's Syndrome in Human Induced Pluripotent Stem Cells
Jonathan Pini, Matthieu Rouleau, Claude Desnuelle, et al.
Bulletin De L'Academie Nationale De Medecine
|
October 26, 2005
[The possible place of autologus cell therapy in facioscapulohumeral muscular dystrophy]
Claude Desnuelle, Sabrina Sacconi, Jean-Pierre Marolleau, et al.
Journal of Neurology
|
July 31, 2009
Do patients having a decrease in SNAP amplitude during the course of MMN present with a different condition?
Emilien Delmont, Charles Benaïm, Mael Launay, et al.
Annals of Physical and Rehabilitation Medicine
|
October 13, 2017
Brain computer interface with the P300 speller: Usability for disabled people with amyotrophic lateral sclerosis
Violaine Guy, Marie-Hélène Soriani, Mariane Bruno, et al.
Journal of Neurology
|
June 19, 2010
Abnormalities of cerebral arteries are frequent in patients with late-onset Pompe disease
Sabrina Sacconi, Jonathan D Bocquet, Stéphane Chanalet, et al.
Journal of Neuroimmunology
|
December 4, 2014
Improving the detection of IgM antibodies against glycolipids complexes of GM1 and Galactocerebroside in Multifocal Motor Neuropathy using glycoarray and ELISA assays
Emilien Delmont, Susan Halstead, Francesc Galban-Horcajo, et al.
Joint Bone Spine
|
October 22, 2010
Chronic ankle instability and common fibular nerve injury
Michaël Benchortane, Hervé Collado, Jean-Marie Coudreuse, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology
|
August 31, 2010
Optimal whole-body vibration settings for muscle strength and power enhancement in human knee extensors
Pierre-David Petit, Manuela Pensini, Joël Tessaro, et al.
Neurology and Therapy
|
November 4, 2015
The European LEMS Registry: Baseline Demographics and Treatment Approaches
Renato Mantegazza, Andreas Meisel, Joern P Sieb, et al.
Neuromuscular Disorders : NMD
|
July 12, 2017
First clinical and genetic description of a family diagnosed with late-onset Pompe disease from Costa Rica
Gabriel Torrealba-Acosta, María Consuelo Rodríguez-Roblero, Sixto Bogantes-Ledezma, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 74) with videos related to
Sort By:
Page
of 8
Stem Cells and Development
|
November 18, 2015
Modeling Andersen's Syndrome in Human Induced Pluripotent Stem Cells
Jonathan Pini, Matthieu Rouleau, Claude Desnuelle, et al.
Bulletin De L'Academie Nationale De Medecine
|
October 26, 2005
[The possible place of autologus cell therapy in facioscapulohumeral muscular dystrophy]
Claude Desnuelle, Sabrina Sacconi, Jean-Pierre Marolleau, et al.
Journal of Neurology
|
July 31, 2009
Do patients having a decrease in SNAP amplitude during the course of MMN present with a different condition?
Emilien Delmont, Charles Benaïm, Mael Launay, et al.
Annals of Physical and Rehabilitation Medicine
|
October 13, 2017
Brain computer interface with the P300 speller: Usability for disabled people with amyotrophic lateral sclerosis
Violaine Guy, Marie-Hélène Soriani, Mariane Bruno, et al.
Journal of Neurology
|
June 19, 2010
Abnormalities of cerebral arteries are frequent in patients with late-onset Pompe disease
Sabrina Sacconi, Jonathan D Bocquet, Stéphane Chanalet, et al.
Journal of Neuroimmunology
|
December 4, 2014
Improving the detection of IgM antibodies against glycolipids complexes of GM1 and Galactocerebroside in Multifocal Motor Neuropathy using glycoarray and ELISA assays
Emilien Delmont, Susan Halstead, Francesc Galban-Horcajo, et al.
Joint Bone Spine
|
October 22, 2010
Chronic ankle instability and common fibular nerve injury
Michaël Benchortane, Hervé Collado, Jean-Marie Coudreuse, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology
|
August 31, 2010
Optimal whole-body vibration settings for muscle strength and power enhancement in human knee extensors
Pierre-David Petit, Manuela Pensini, Joël Tessaro, et al.
Neurology and Therapy
|
November 4, 2015
The European LEMS Registry: Baseline Demographics and Treatment Approaches
Renato Mantegazza, Andreas Meisel, Joern P Sieb, et al.
Neuromuscular Disorders : NMD
|
July 12, 2017
First clinical and genetic description of a family diagnosed with late-onset Pompe disease from Costa Rica
Gabriel Torrealba-Acosta, María Consuelo Rodríguez-Roblero, Sixto Bogantes-Ledezma, et al.
Page
of 8