Livia Pisciotta - Dissemin

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All papers authored by Livia Pisciotta

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2024 Elisa Proietti

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, Fabio Rapallo

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, Elena Molinari, Viviana Mucci, Lucio Marinelli

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, Consuelo Borgarelli

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, Bruno Burlando

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, Livia Pisciotta

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, Ilaria Demori

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Online Questionnaire with Fibromyalgia Patients Shows Negative Correlations between Disease Severity and Adherence to Mediterranean Diet

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2023 Cristina Pederiva

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, Marta Gazzotti, Marcello Arca

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, Maurizio Averna, Giuseppe Banderali, Giacomo Biasucci

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, Marta Brambilla, Paola Buonuomo, Paolo Calabrò

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, Francesco Cipollone, Nadia Citroni, Sergio D’Addato

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, Maria Del Ben

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, Simonetta Genovesi

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, Ornella Guardamagna and 23 other authors

Clinical Approach in the Management of Paediatric Patients with Familial Hypercholesterolemia: A National Survey Conducted by the LIPIGEN Paediatric Group

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2021 Samir Giuseppe Sukkar, Ludovica Cogorno, Livia Pisciotta

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, Andrea Pasta, Antonio Vena, Raffaella Gradaschi, Chiara Dentone

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, Erica Guiddo, Eleonora Martino, Sabrina Beltramini, Lorenzo Maria Donini, Luca Carmisciano, Maria Pia Sormani, Matteo Bassetti

Clinical efficacy of eucaloric ketogenic nutrition in the COVID-19 cytokine storm: A retrospective analysis of mortality and intensive care unit admission

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2018 Marco Canepa

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, Nathan Artom, Pietro Ameri, Federico Carbone

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, Fabrizio Montecucco

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, Giorgio Ghigliotti

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, Claudio Brunelli, Franco Dallegri, Aldo Pende, Livia Pisciotta

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Short-term effect of rosuvastatin treatment on arterial stiffness in individuals with newly-diagnosed heterozygous familial hypercholesterolemia

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2017 Livia Pisciotta, Giulia Tozzi, Lorena Travaglini

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, Roberta Taurisano, Tiziano Lucchi

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, Giuseppe Indolfi, Francesco Papadia, Maja Di Rocco, Lorenzo D'Antiga, Patricia Crock, Komal Vora, Scott Nightingale, Helen Michelakakis, Anastasia Garoufi, Lilia Lykopoulou and 2 other authors

Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variants

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2015 Livia Pisciotta, Cecilia Vitali, Elda Favari, Paola Fossa, Maria Pia Adorni, Daniela Leone, Nathan Artom, Raffaele Fresa, Laura Calabresi, Sebastiano Calandra, Stefano Bertolini

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A Complex Phenotype in A Child with Familial HDL Deficiency Due to A Novel Frameshift Mutation in APOA1 Gene (apoA-IGuastalla)

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