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Journal of Neuropathology and Experimental Neurology|May 1, 1997
Transforming growth factor-beta 1 in polymyositis and dermatomyositis correlates with fibrosis but not with mononuclear cell infiltrateP Confalonieri, P Bernasconi, F Cornelio, et al.
Journal of Neurology|May 1, 1997
Inflammatory myopathies and systemic disorders: a review of immunopathogenetic mechanisms and clinical featuresR Mantegazza, P Bernasconi, P Confalonieri, et al.
European Neurology|January 1, 1997
Emerging treatments in myopathiesC Antozzi, P Confalonieri, R Mantegazza, et al.
Journal of Neuroimmunology|October 1, 1993
Immune activation in myasthenia gravis: soluble interleukin-2 receptor, interferon-gamma and tumor necrosis factor-alpha levels in patients' serumP Confalonieri, C Antozzi, F Cornelio, et al.
Journal of Neurology|February 1, 1994
Changes in peripheral blood lymphocyte subset frequencies in myasthenia gravis patients are related to immunosuppressionF Crosti, M Armanini, P Confalonieri, et al.
Journal of Neuropathology and Experimental Neurology|April 5, 2000
Increased expression of beta-chemokines in muscle of patients with inflammatory myopathiesP Confalonieri, P Bernasconi, P Megna, et al.
Journal of Neuroimmunology|June 17, 1998
The expression of co-stimulatory and accessory molecules on cultured human muscle cells is not dependent on stimulus by pro-inflammatory cytokines: relevance for the pathogenesis of inflammatory myopathyP Bernasconi, P Confalonieri, F Andreetta, et al.
Italian Journal of Neurological Sciences|October 1, 1994
The POEMS syndrome: report of six casesD Pareyson, R Marazzi, P Confalonieri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2006
A post-marketing study on immunomodulating treatments for relapsing-remitting multiple sclerosis in Lombardia: preliminary resultsC Milanese, E Beghi, L Giordano, et al.
Human Mutation|October 26, 1999
Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenitaR Brugnoni, S Galantini, P Confalonieri, et al.
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