Search Results - Daniel Viglietti~

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  1. 1
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    A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature by Daniele Zama, Giulia Giulietti, Edoardo Muratore, Immacolata Andolfo, Roberta Russo, Achille Iolascon, Andrea Pession

    Published 2020
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  2. 2
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    All You Need Is Evidence: What We Know About Pneumonia in Children With Neuromuscular Diseases by Claudio Cherchi, Claudio Cherchi, Maria B. Chiarini Testa, Maria B. Chiarini Testa, Daniele Deriu, Alessandra Schiavino, Alessandra Schiavino, Francesca Petreschi, Francesca Petreschi, Nicola Ullmann, Nicola Ullmann, Maria G. Paglietti, Maria G. Paglietti, Renato Cutrera, Renato Cutrera

    Published 2021
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    Ichthyosis Prematurity Syndrome due to a Novel SLC27A4 Homozygous Mutation in an Italian Patient by Andrea Diociaiuti, Enrico Rosati, Maria Giovanna Paglietti, Paola Vacca, Renata Boldrini, Elisa Pisaneschi, Daniele Castiglia, Antonio Novelli, Maya El Hachem

    Published 2018
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    Stopping bDMARDs at the beginning of pregnancy is associated with disease flares and preterm delivery in women with rheumatoid arthritis by Maria Chiara Gerardi, Francesca Crisafulli, Antía García-Fernandez, Daniele Lini, Chiara Bazzani, Ilaria Cavazzana, Matteo Filippini, Micaela Fredi, Roberto Gorla, Maria Grazia Lazzaroni, Cecilia Nalli, Marco Taglietti, Andrea Lojacono, Francesca Ramazzotto, Cristina Zanardini, Sonia Zatti, Franco Franceschini, Angela Tincani, Laura Andreoli

    Published 2022
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