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Neuromuscular Disorders : NMD|June 18, 2013
Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiencyS Nouioua, D Cheillan, S Zaouidi, et al.Neuromuscular Disorders : NMD|June 11, 2013
Scoliosis in Duchenne muscular dystrophy (DMD)John D Hsu, Ros QuinlivanNeuromuscular Disorders : NMD|March 8, 2013
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: a clinical and muscle MRI studyM Masciullo, E Iannaccone, M L E Bianchi, et al.Neuromuscular Disorders : NMD|April 10, 2013
Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in The NetherlandsXenia L Stalpers, Aad Verrips, Bwee Tien Poll-The, et al.Neuromuscular Disorders : NMD|June 2, 2012
The first Italian patient with oculopharyngodistal myopathy: case report and considerations on differential diagnosisAndrea Mignarri, Maria Alessandra Carluccio, Alessandro Malandrini, et al.Neuromuscular Disorders : NMD|May 19, 2012
Myalgic phenotype and preserved muscle strength in adult-onset acid maltase deficiencyLyell K Jones, Teerin Liewluck, Ralitza H GavrilovaNeuromuscular Disorders : NMD|December 4, 2012
Myopathy in a rhesus monkey with biopsy findings similar to human sporadic inclusion body myositisDaniel Skuk, Marlyne Goulet, Martin Paradis, et al.Neuromuscular Disorders : NMD|November 28, 2012
Magnetic resonance imaging and spectroscopy in the evaluation of neuromuscular disorders and fatigueCaterina Tonon, Laura Ludovica Gramegna, Raffaele LodiNeuromuscular Disorders : NMD|December 5, 2013
Exome sequencing identifies Laing distal myopathy MYH7 mutation in a Roma family previously diagnosed with distal neuronopathyKatalin Komlósi, Kinga Hadzsiev, Lutz Garbes, et al.Neuromuscular Disorders : NMD|December 7, 2013
Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle diseaseJ McC Howell, K R Walker, K E Creed, et al.Pageof 341