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Recherche En Soins Infirmiers|November 19, 2013
[What a tracheostomy changes in a child with a neuromuscular disease]Brigitte Rul, Susana Quijano-Roy, Anne Golse, et al.Neuromuscular Disorders : NMD|June 1, 2007
Isokinetic muscle testing for weak patients suffering from neuromuscular disorders: a reliability studyVincent Tiffreau, Isabelle Ledoux, Bruno Eymard, et al.Journal of Medical Case Reports|March 26, 2022
Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: a case reportMohamed Islam Kediha, Meriem Tazir, Damien Sternberg, et al.Neuromuscular Disorders : NMD|August 8, 2015
Atypical nuclear abnormalities in a patient with Brody diseaseJean-Marie Mussini, Armelle Magot, Daniel Hantaï, et al.British Journal of Clinical Pharmacology|February 3, 2011
Riluzole pharmacokinetics in young patients with spinal muscular atrophyChadi Abbara, Brigitte Estournet, Lucette Lacomblez, et al.Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|August 8, 2006
Long-term results of cricopharyngeal myotomy in oculopharyngeal muscular dystrophyLaurent Coiffier, Sophie Périé, Pascal Laforêt, et al.Journal of Neuromuscular Diseases|November 11, 2017
Congenital Myasthenic Syndromes or Inherited Disorders of Neuromuscular Transmission: Recent Discoveries and Open QuestionsSophie Nicole, Yoshiteru Azuma, Stéphanie Bauché, et al.BMC Neurology|August 23, 2015
Prevalence and correlates of apathy in myotonic dystrophy type 1Benjamin Gallais, Michèle Montreuil, Marcela Gargiulo, et al.Gait & Posture|November 6, 2007
Compensatory mechanisms during walking in response to muscle weakness in spinal muscular atrophy, type IIIZlatko Matjacić, Andrej Olensek, Janez Krajnik, et al.Neuromuscular Disorders : NMD|April 17, 2007
Cognitive profile in childhood myotonic dystrophy type 1: is there a global impairment?Nathalie Angeard, Marcela Gargiulo, Aurélia Jacquette, et al.Pageof 26