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Journal of Clinical Neuromuscular Disease|August 23, 2017
Clinical and Laboratory Profiles of Idiopathic Small Fiber Neuropathy in Children: Case SeriesJafar Kafaie, Ali Al Balushi, Minsoo Kim, et al.
Neuropathology and Applied Neurobiology|March 3, 2023
Schwann cells and myelin in human peripheral nerve: Major protein components vary with age, axon size and pathologyAlan Pestronk, Robert E Schmidt, Robert Bucelli, et al.
Muscle & Nerve|January 28, 2003
Sensory neuropathy with monoclonal IgM binding to a trisulfated heparin disaccharideAlan Pestronk, Rati Choksi, Eric Logigian, et al.
Muscle & Nerve|July 2, 2013
Cramps and small-fiber neuropathyGlenn Lopate, Elizabeth Streif, Matthew Harms, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 12, 2007
Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutationsRobert H Baloh, Robert E Schmidt, Alan Pestronk, et al.
Human Molecular Genetics|December 3, 2005
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradationConrad C Weihl, Seema Dalal, Alan Pestronk, et al.
Arthritis and Rheumatism|April 29, 2006
Brachio-cervical inflammatory myopathies: clinical, immune, and myopathologic featuresAlan Pestronk, Ksenija Kos, Glenn Lopate, et al.
Muscle & Nerve|June 20, 2008
Calibrated quantitative ultrasound imaging of skeletal muscle using backscatter analysisCraig M Zaidman, Mark R Holland, Christian C Anderson, et al.
Muscle & Nerve|July 24, 2015
Nerve ultrasound identifies abnormalities in the posterior interosseous nerve in patients with proximal radial neuropathiesAlexander R Dietz, Robert C Bucelli, Alan Pestronk, et al.
Human Molecular Genetics|March 3, 2007
Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in miceConrad C Weihl, Sara E Miller, Phyllis I Hanson, et al.
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