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Neuromuscular Disorders : NMD|June 24, 2018
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathyAndrew R Findlay, Matthew B Harms, Alan Pestronk, et al.Acta Neuropathologica|October 7, 2006
The muscle protein dysferlin accumulates in the Alzheimer brainJames E Galvin, Divya Palamand, Jeff Strider, et al.Neurology|March 22, 2019
Immune myopathy with large histiocyte-related myofiber necrosisAlan Pestronk, Namita Sinha, Ziad Alhumayyd, et al.Journal of Neuroimmunology|June 5, 2002
Complement 3 deficiency and oral prednisolone improve strength and prolong survival of laminin alpha2-deficient miceAnne M Connolly, Richard M Keeling, Elizabeth M Streif, et al.Orphanet Journal of Rare Diseases|June 22, 2025
Dysferlinopathy as cause of long-term hyperCKemia with preserved strengthIkreet Cheema, Jacob Goodwin, Teerin Liewluck, et al.Muscle & Nerve|August 26, 2009
Cardiac pathology exceeds skeletal muscle pathology in two cases of limb-girdle muscular dystrophy type 2IMarta Margeta, Anne M Connolly, Thomas L Winder, et al.Muscle & Nerve|March 7, 2026
Integrating Serum Neurofilament Light Chain Into Amyotrophic Lateral Sclerosis Diagnostic CriteriaSean E Smith, Timothy M Miller, Andrew Atkinson, et al.Neurology|April 5, 2013
Detection of peripheral nerve pathology: comparison of ultrasound and MRICraig M Zaidman, Michael J Seelig, Jonathan C Baker, et al.Muscle & Nerve|November 22, 2012
Newborn brachial plexus palsy: evaluation of severity using quantitative ultrasound of muscleCraig M Zaidman, Mark R Holland, Michael J Noetzel, et al.Neuromuscular Disorders : NMD|September 7, 2010
Quantitative ultrasound using backscatter analysis in Duchenne and Becker muscular dystrophyCraig M Zaidman, Anne M Connolly, Elizabeth C Malkus, et al.Pageof 14