Search Results - Patrizia Bergonzini

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    Grisel's Syndrome in Children: Two Case Reports and Systematic Review of the Literature by Nicole Pini, Martina Ceccoli, Patrizia Bergonzini, Lorenzo Iughetti

    Published 2020
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    EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report by Ilaria Filareto, Giulia Cinelli, Ilaria Scalabrini, Elisa Caramaschi, Patrizia Bergonzini, Elisabetta Spezia, Alessandra Todeschini, Lorenzo Iughetti

    Published 2022
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