Clinical Health Care during the COVID-19 Pandemic

Tekijä Luigetti, Marco, Frisullo, Giovanni
Julkaisussa J Clin Med (2020)

Nerve Biopsy in Peripheral Neuropathies: Not All Water Is under the Bridge

Tekijä Luigetti, Marco, Di Paolantonio, Andrea
Julkaisussa Brain Sci (2021)

Peripheral Nervous System Involvement in Lymphoproliferative Disorders

Tekijä Sabatelli, Mario, Laurenti, Luca, Luigetti, Marco
Julkaisussa Mediterr J Hematol Infect Dis (2018)

Reassessing IVIg therapy in chronic inflammatory demyelinating polyradiculoneuropathy during COVID-19: a chance to verify the need for chronic maintenance therapy

Tekijä Romozzi, Marina, Bisogni, Giulia, Sabatelli, Mario, Luigetti, Marco
Julkaisussa Neurol Sci (2021)

Diagnosis and Treatment of Hereditary Transthyretin Amyloidosis (hATTR) Polyneuropathy: Current Perspectives on Improving Patient Care

Tekijä Luigetti, Marco, Romano, Angela, Di Paolantonio, Andrea, Bisogni, Giulia, Sabatelli, Mario
Julkaisussa Ther Clin Risk Manag (2020)

Pathological Findings in Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Single-Center Experience

Tekijä Luigetti, Marco, Romano, Angela, Di Paolantonio, Andrea, Bisogni, Giulia, Rossi, Salvatore, Conte, Amelia, Madia, Francesca, Sabatelli, Mario
Julkaisussa Brain Sci (2020)

Small Fibre Involvement in Multifocal Motor Neuropathy Explored with Sudoscan: A Single-Centre Experience

Tekijä Luigetti, Marco, Giovannini, Silvia, Romano, Angela, Bisogni, Giulia, Barbato, Francesco, Di Paolantonio, Andrea, Servidei, Serenella, Granata, Giuseppe, Sabatelli, Mario
Julkaisussa Diagnostics (Basel) (2020)

Ocular Involvement in Hereditary Transthyretin Amyloidosis: A Case Series Describing Novel Potential Biomarkers

Tekijä Minnella, Angelo Maria, Rissotto, Roberta, Maceroni, Martina, Romano, Angela, Fasciani, Romina, Luigetti, Marco, Sabatelli, Mario, Rizzo, Stanislao, Falsini, Benedetto
Julkaisussa Genes (Basel) (2021)

Restless Leg Syndrome in Different Types of Demyelinating Neuropathies: A Single-Center Pilot Study

Tekijä Luigetti, Marco, Del Grande, Alessandra, Testani, Elisa, Bisogni, Giulia, Losurdo, Anna, Giannantoni, Nadia Mariagrazia, Mazza, Salvatore, Sabatelli, Mario, Della Marca, Giacomo
Julkaistu 2013

Pediatric Motor Inflammatory Neuropathy: The Role of Antiphospholipid Antibodies

Tekijä Brogna, Claudia, Luigetti, Marco, Norcia, Giulia, Scalise, Roberta, Ferrantini, Gloria, Berti, Beatrice, Romeo, Domenico M., Manna, Raffaele, Mercuri, Eugenio, Pane, Marika
Julkaisussa Brain Sci (2020)

Ocular Involvement in Hereditary Amyloidosis

Tekijä Minnella, Angelo Maria, Rissotto, Roberta, Antoniazzi, Elena, Di Girolamo, Marco, Luigetti, Marco, Maceroni, Martina, Bacherini, Daniela, Falsini, Benedetto, Rizzo, Stanislao, Obici, Laura
Julkaisussa Genes (Basel) (2021)

Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis

Tekijä Iorio, Andrea, De Angelis, Flavio, Di Girolamo, Marco, Luigetti, Marco, Pradotto, Luca G., Mazzeo, Anna, Frusconi, Sabrina, My, Filomena, Manfellotto, Dario, Fuciarelli, Maria, Polimanti, Renato
Julkaisussa BMC Genomics (2017)

Patisiran in hATTR Amyloidosis: Six-Month Latency Period before Efficacy

Tekijä Gentile, Luca, Russo, Massimo, Luigetti, Marco, Bisogni, Giulia, Di Paolantonio, Andrea, Romano, Angela, Guglielmino, Valeria, Arimatea, Ilenia, Sabatelli, Mario, Toscano, Antonio, Vita, Giuseppe, Mazzeo, Anna
Julkaisussa Brain Sci (2021)

Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis

Tekijä De Lillo, Antonella, Pathak, Gita A., De Angelis, Flavio, Di Girolamo, Marco, Luigetti, Marco, Sabatelli, Mario, Perfetto, Federico, Frusconi, Sabrina, Manfellotto, Dario, Fuciarelli, Maria, Polimanti, Renato
Julkaisussa Clin Epigenetics (2020)

Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis

Tekijä Iorio, Andrea, De Lillo, Antonella, De Angelis, Flavio, Di Girolamo, Marco, Luigetti, Marco, Sabatelli, Mario, Pradotto, Luca, Mauro, Alessandro, Mazzeo, Anna, Stancanelli, Claudia, Perfetto, Federico, Frusconi, Sabrina, My, Filomena, Manfellotto, Dario, Fuciarelli, Maria, Polimanti, Renato
Julkaisussa Eur J Hum Genet (2017)

hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers

Tekijä Luigetti, Marco, Romozzi, Marina, Bisogni, Giulia, Cardellini, Davide, Cavallaro, Tiziana, Di Paolantonio, Andrea, Fabrizi, Gian Maria, Fenu, Silvia, Gentile, Luca, Grandis, Marina, Marucci, Gianluca, Massucco, Sara, Mazzeo, Anna, Pareyson, Davide, Romano, Angela, Russo, Massimo, Schenone, Angelo, Tagliapietra, Matteo, Tozza, Stefano, Vita, Giuseppe, Sabatelli, Mario
Julkaisussa Brain Sci (2020)

Nerve ultrasound in hereditary transthyretin amyloidosis: red flags and possible progression biomarkers

Tekijä Salvalaggio, Alessandro, Coraci, Daniele, Cacciavillani, Mario, Obici, Laura, Mazzeo, Anna, Luigetti, Marco, Pastorelli, Francesca, Grandis, Marina, Cavallaro, Tiziana, Bisogni, Giulia, Lozza, Alessandro, Gemelli, Chiara, Gentile, Luca, Ermani, Mario, Fabrizi, Gian Maria, Plasmati, Rosaria, Campagnolo, Marta, Castellani, Francesca, Gasparotti, Roberto, Martinoli, Carlo, Padua, Luca, Briani, Chiara
Julkaisussa J Neurol (2020)

ATTRv in Lazio-Italy: A High-Prevalence Region in a Non-Endemic Country

Tekijä Luigetti, Marco, Guglielmino, Valeria, Antonini, Giovanni, Casali, Carlo, Ceccanti, Marco, Chiappini, Maria Grazia, De Giglio, Laura, Di Lazzaro, Vincenzo, Di Muzio, Antonio, Goglia, Mariangela, Inghilleri, Maurizio, Leonardi, Luca, Massa, Roberto, Pennisi, Elena Maria, Petrucci, Antonio, Proietti, Emanuela, Rispoli, Marianna, Sabatelli, Mario, Di Girolamo, Marco
Julkaisussa Genes (Basel) (2021)

Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy

Tekijä Magliano, Lorenza, Obici, Laura, Sforzini, Claudia, Mazzeo, Anna, Russo, Massimo, Cappelli, Francesco, Fenu, Silvia, Luigetti, Marco, Tagliapietra, Matteo, Gemelli, Chiara, Leonardi, Luca, Tozza, Stefano, Pradotto, Luca Guglielmo, Citarelli, Giulia, Mauro, Alessandro, Manganelli, Fiore, Antonini, Giovanni, Grandis, Marina, Fabrizi, Gian Maria, Sabatelli, Mario, Pareyson, Davide, Perfetto, Federico, Merlini, Giampaolo, Vita, Giuseppe
Julkaisussa Orphanet J Rare Dis (2021)

A multicentre retrospective study of Charcot-Marie-Tooth disease type 4B (CMT4B) due to mutations in Myotubularin-related proteins (MTMRs)

Tekijä Pareyson, Davide, Stojkovic, Tanya, Reilly, Mary M., Leonard-Louis, Sarah, Laurà, Matilde, Blake, Julian, Parman, Yesim, Battaloglu, Esra, Tazir, Meriem, Bellatache, Mounia, Bonello-Palot, Nathalie, Lévy, Nicolas, Sacconi, Sabrina, Guimarães-Costa, Raquel, Attarian, Sharham, Latour, Philippe, Solé, Guilhem, Megarbane, André, Horvath, Rita, Ricci, Giulia, Choi, Byung-Ok, Schenone, Angelo, Gemelli, Chiara, Geroldi, Alessandro, Sabatelli, Mario, Luigetti, Marco, Santoro, Lucio, Manganelli, Fiore, Quattrone, Aldo, Valentino, Paola, Murakami, Tatsufumi, Scherer, Steven S., Dankwa, Lois, Shy, Michael E., Bacon, Chelsea J, Herrmann, David N., Zambon, Alberto, Tramacere, Irene, Pisciotta, Chiara, Magri, Stefania, Previtali, Stefano C., Bolino, Alessandra
Julkaisussa Ann Neurol (2019)