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Journal of Neuropathology and Experimental Neurology|December 6, 2019
Chronic Graft Versus Host Myopathies: Noninflammatory, Multi-Tissue Pathology With Glycosylation DisordersAlan PestronkCurrent Opinion in Rheumatology|September 22, 2011
Acquired immune and inflammatory myopathies: pathologic classificationAlan PestronkJournal of Neuroimmunology|October 13, 2022
Sarcoidosis, granulomas and myopathy syndromes: A clinical-pathology reviewMark Garret, Alan PestronkMuscle & Nerve|December 21, 2020
Treatable, motor-sensory, axonal neuropathies with C5b-9 complement on endoneurial microvesselsBhavesh Trikamji, Alan PestronkJournal of Neuropathology and Experimental Neurology|August 7, 2021
Pathology Features of Immune and Inflammatory Myopathies, Including a Polymyositis Pattern, Relate Strongly to Serum AutoantibodiesAlan Pestronk, Rati ChoksiCurrent Treatment Options in Neurology|January 19, 2011
Inflammatory demyelinating neuropathiesGlenn Lopate, Alan PestronkSeminars in Neurology|August 2, 2003
Antibody-associated polyneuropathy syndromes: principles and treatmentAndrew J Kornberg, Alan PestronkNeurology(R) Neuroimmunology & Neuroinflammation|January 24, 2018
Immune myopathies with perimysial pathology: Clinical and laboratory featuresRobert C Bucelli, Alan PestronkMuscle & Nerve|March 12, 2014
Nerve size in chronic inflammatory demyelinating neuropathy varies with disease activity and therapy response over time: a retrospective ultrasound studyCraig M Zaidman, Alan PestronkCurrent Opinion in Neurology|July 29, 2010
Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkersConrad C Weihl, Alan PestronkPageof 14