Showing 1 - 2 results of 2 for search 'L. Magnani', query time: 0.01s Refine Results
  1. 1
    Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene

    Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene by E. Conticini, A. Negro, L. Magnani, R. Ugolini, B. Atienza-Mateo, B. Frediani, C. Salvarani

    Published 2020
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  2. 2
    Disease activity assessment in large vessel vasculitis

    Disease activity assessment in large vessel vasculitis by N. Pipitone, G. Bajocchi, D. Formisano, L. Pulsatelli, R. Meliconi, G. Germanò, D. Salvo, M. Casali, A. Versari, L. Magnani, L. Boiardi, C. Salvarani

    Published 2011
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