Showing results (1521-1530 of 3,399) with videos related to

Sort By:
Pageof 340
Neuromuscular Disorders : NMD|August 21, 2018
A recurrent de novo DYNC1H1 tail domain mutation causes spinal muscular atrophy with lower extremity predominance, learning difficulties and mild brain abnormalitySophelia Hoi Shan Chan, Nens van Alfen, Inger Johanne Thuestad, et al.
Neuromuscular Disorders : NMD|April 29, 2019
Unraveling upper extremity performance in Duchenne muscular dystrophy: A biophysical modelMariska M H P Janssen, Jaap Harlaar, Bart Koopman, et al.
Neuromuscular Disorders : NMD|April 29, 2019
A review of the histopathological findings in myasthenia gravis: Clues to the pathogenesis of treatment-resistance in extraocular musclesTarin A Europa, Melissa Nel, Jeannine M Heckmann
Neuromuscular Disorders : NMD|May 2, 2019
Exome sequencing detects compound heterozygous nonsense LAMA2 mutations in two siblings with atypical phenotype and nearly normal brain MRISimona Saredi, Sara Gibertini, Leslie Matalonga, et al.
Neuromuscular Disorders : NMD|January 30, 2022
DMD exon 2 duplication due to a complex genomic rearrangement is associated with a somatic mosaicismAkatsuki Kubota, Hiroyuki Ishiura, Kristine Joyce Linay Porto, et al.
Neuromuscular Disorders : NMD|February 4, 2022
Biomarkers of disease progression in adolescents and adults with 5q spinal muscular atrophy: a systematic review and meta-analysisMaria Gavriilaki, Maria Moschou, Vasileios Papaliagkas, et al.
Neuromuscular Disorders : NMD|September 1, 2018
A novel MYH7 founder mutation causing Laing distal myopathy in Southern SpainP Carbonell-Corvillo, E Tristán-Clavijo, M Cabrera-Serrano, et al.
Neuromuscular Disorders : NMD|September 3, 2018
Lower-extremity magnetic resonance imaging in patients with hyperkalemic periodic paralysis carrying the SCN4A mutation T704M: 30-month follow-up of seven patientsHa-Neul Jeong, Ji Sook Yi, Young Han Lee, et al.
Neuromuscular Disorders : NMD|October 2, 2018
Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1Claudia Cutellè, Emanuele Rastelli, Manuela Gibellini, et al.
Neuromuscular Disorders : NMD|October 29, 2021
Whole-body muscle MRI in McArdle diseaseDavid Tobaly, Pascal Laforêt, Tanya Stojkovic, et al.
Pageof 340