Search Results - L. Magnani

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    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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    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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