8 results on '"Doneddu, Pietro Emiliano"'
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2. Unclassified clinical presentations of chronic inflammatory demyelinating polyradiculoneuropathy
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Doneddu, Pietro Emiliano, primary, Akyil, Houseyin, additional, Manganelli, Fiore, additional, Briani, Chiara, additional, Cocito, Dario, additional, Benedetti, Luana, additional, Mazzeo, Anna, additional, Fazio, Raffaella, additional, Filosto, Massimiliano, additional, Cosentino, Giuseppe, additional, Di Stefano, Vincenzo, additional, Antonini, Giovanni, additional, Marfia, Girolama Alessandra, additional, Inghilleri, Maurizio, additional, Siciliano, Gabriele, additional, Clerici, Angelo Maurizio, additional, Carpo, Marinella, additional, Schenone, Angelo, additional, Luigetti, Marco, additional, Lauria, Giuseppe, additional, Matà, Sabrina, additional, Rosso, Tiziana, additional, Minicuci, Giacomo Maria, additional, Lucchetta, Marta, additional, Cavaletti, Guido, additional, Liberatore, Giuseppe, additional, Spina, Emanuele, additional, Campagnolo, Marta, additional, Peci, Erdita, additional, Germano, Francesco, additional, Gentile, Luca, additional, Strano, Camilla, additional, Cotti Piccinelli, Stefano, additional, Vegezzi, Elisa, additional, Leonardi, Luca, additional, Mataluni, Giorgia, additional, Ceccanti, Marco, additional, Schirinzi, Erika, additional, Romozzi, Marina, additional, and Nobile-Orazio, Eduardo, additional
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- 2023
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3. Comparison of the diagnostic accuracy of the 2021 EAN/PNS and 2010 EFNS/PNS diagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy
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Doneddu, Pietro Emiliano, primary, De Lorenzo, Alberto, additional, Manganelli, Fiore, additional, Cocito, Dario, additional, Fazio, Raffaella, additional, Briani, Chiara, additional, Mazzeo, Anna, additional, Filosto, Massimiliano, additional, Cosentino, Giuseppe, additional, Benedetti, Luana, additional, Schenone, Angelo, additional, Marfia, Girolama Alessandra, additional, Antonini, Giovanni, additional, Matà, Sabrina, additional, Luigetti, Marco, additional, Liberatore, Giuseppe, additional, Spina, Emanuele, additional, Peci, Erdita, additional, Strano, Camilla, additional, Cacciavillani, Mario, additional, Gentile, Luca, additional, Cotti Piccinelli, Stefano, additional, Cortese, Andrea, additional, Bianchi, Elisa, additional, and Nobile-Orazio, Eduardo, additional
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- 2022
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4. Guillain-Barré syndrome and COVID-19: an observational multicentre study from two Italian hotspot regions
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Filosto, Massimiliano, primary, Cotti Piccinelli, Stefano, additional, Gazzina, Stefano, additional, Foresti, Camillo, additional, Frigeni, Barbara, additional, Servalli, Maria Cristina, additional, Sessa, Maria, additional, Cosentino, Giuseppe, additional, Marchioni, Enrico, additional, Ravaglia, Sabrina, additional, Briani, Chiara, additional, Castellani, Francesca, additional, Zara, Gabriella, additional, Bianchi, Francesca, additional, Del Carro, Ubaldo, additional, Fazio, Raffaella, additional, Filippi, Massimo, additional, Magni, Eugenio, additional, Natalini, Giuseppe, additional, Palmerini, Francesco, additional, Perotti, Anna Maria, additional, Bellomo, Andrea, additional, Osio, Maurizio, additional, Scopelliti, Giuseppe, additional, Carpo, Marinella, additional, Rasera, Andrea, additional, Squintani, Giovanna, additional, Doneddu, Pietro Emiliano, additional, Bertasi, Valeria, additional, Cotelli, Maria Sofia, additional, Bertolasi, Laura, additional, Fabrizi, Gian Maria, additional, Ferrari, Sergio, additional, Ranieri, Federico, additional, Caprioli, Francesca, additional, Grappa, Elena, additional, Broglio, Laura, additional, De Maria, Giovanni, additional, Leggio, Ugo, additional, Poli, Loris, additional, Rasulo, Frank, additional, Latronico, Nicola, additional, Nobile-Orazio, Eduardo, additional, Padovani, Alessandro, additional, and Uncini, Antonino, additional
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- 2020
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5. Frequency of diabetes and other comorbidities in chronic inflammatory demyelinating polyradiculoneuropathy and their impact on clinical presentation and response to therapy
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Doneddu, Pietro Emiliano, primary, Cocito, Dario, additional, Manganelli, Fiore, additional, Fazio, Raffaella, additional, Briani, Chiara, additional, Filosto, Massimiliano, additional, Benedetti, Luana, additional, Bianchi, Elisa, additional, Jann, Stefano, additional, Mazzeo, Anna, additional, Antonini, Giovanni, additional, Cosentino, Giuseppe, additional, Marfia, Girolama Alessandra, additional, Cortese, Andrea, additional, Clerici, Angelo Maurizio, additional, Carpo, Marinella, additional, Schenone, Angelo, additional, Siciliano, Gabriele, additional, Luigetti, Marco, additional, Lauria, Giuseppe, additional, Rosso, Tiziana, additional, Cavaletti, Guido, additional, Beghi, Ettore, additional, Liberatore, Giuseppe, additional, Santoro, Lucio, additional, Spina, Emanuele, additional, Peci, Erdita, additional, Tronci, Stefano, additional, Ruiz, Marta, additional, Cotti Piccinelli, Stefano, additional, Verrengia, Elena Pinuccia, additional, Gentile, Luca, additional, Leonardi, Luca, additional, Mataluni, Giorgia, additional, Piccolo, Laura, additional, and Nobile-Orazio, Eduardo, additional
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- 2020
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6. Atypical CIDP: diagnostic criteria, progression and treatment response. Data from the Italian CIDP Database
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Doneddu, Pietro Emiliano, primary, Cocito, Dario, additional, Manganelli, Fiore, additional, Fazio, Raffaella, additional, Briani, Chiara, additional, Filosto, Massimiliano, additional, Benedetti, Luana, additional, Mazzeo, Anna, additional, Marfia, Girolama Alessandra, additional, Cortese, Andrea, additional, Fierro, Brigida, additional, Jann, Stefano, additional, Beghi, Ettore, additional, Clerici, Angelo Maurizio, additional, Carpo, Marinella, additional, Schenone, Angelo, additional, Luigetti, Marco, additional, Lauria, Giuseppe, additional, Antonini, Giovanni, additional, Rosso, Tiziana, additional, Siciliano, Gabriele, additional, Cavaletti, Guido, additional, Liberatore, Giuseppe, additional, Santoro, Lucio, additional, Peci, Erdita, additional, Tronci, Stefano, additional, Ruiz, Marta, additional, Cotti Piccinelli, Stefano, additional, Toscano, Antonio, additional, Mataluni, Giorgia, additional, Piccolo, Laura, additional, Cosentino, Giuseppe, additional, Sabatelli, Mario, additional, and Nobile-Orazio, Eduardo, additional
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- 2018
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7. Atypical CIDP: diagnostic criteria, progression and treatment response. Data from the Italian CIDP Database.
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Doneddu, Pietro Emiliano, Cocito, Dario, Manganelli, Fiore, Fazio, Raffaella, Briani, Chiara, Filosto, Massimiliano, Benedetti, Luana, Mazzeo, Anna, Marfia, Girolama Alessandra, Cortese, Andrea, Fierro, Brigida, Jann, Stefano, Beghi, Ettore, Clerici, Angelo Maurizio, Carpo, Marinella, Schenone, Angelo, Luigetti, Marco, Lauria, Giuseppe, Antonini, Giovanni, and Rosso, Tiziana
- Subjects
DISEASE duration ,FATHERS ,SYMPTOMS - Abstract
Objectives: A few variants of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) have been described, but their frequency and evolution to typical CIDP remain unclear. To determine the frequency and characteristics of the CIDP variants, their possible evolution to typical CIDP, and treatment response.Methods: We applied a set of diagnostic criteria to 460 patients included in a database of Italian patients with CIDP. Clinical characteristics and treatment response were reviewed for each patient. The Kaplan-Meier curve was used to estimate the progression rate from atypical to typical CIDP.Results: At the time of inclusion, 376 (82%) patients had a diagnosis of typical CIDP while 84 (18%) had atypical CIDP, including 34 (7%) with distal acquired demyelinating symmetric neuropathy (DADS), 17 (4%) with purely motor, 17 (4%) with Lewis-Sumner syndrome (LSS) and 16 (3.5%) with purely sensory CIDP. Based on retrospective review of the symptoms and signs present at onset and for at least 1 year, 180 (39%) patients had an initial diagnosis compatible with atypical CIDP that in 96 (53%) patients evolved to typical CIDP. Mean disease duration was longer in patients evolving to typical CIDP than in those not evolving (p=0.0016). Patients with DADS and LSS had a less frequent response to immunoglobulin than those with typical CIDP, while patients with purely motor and sensory CIDP had a similar treatment response.Conclusions: The proportion of patients with atypical CIDP varies during the disease course. DADS and LSS have a less frequent response to intravenous immunoglobulin compared with typical CIDP, raising the possibility of a different underlying pathogenetic mechanism. [ABSTRACT FROM AUTHOR]- Published
- 2019
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8. Atypical CIDP: diagnostic criteria, progression and treatment response. Data from the Italian CIDP Database
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Pietro Emiliano, Doneddu, Dario, Cocito, Fiore, Manganelli, Raffaella, Fazio, Chiara, Briani, Massimiliano, Filosto, Luana, Benedetti, Anna, Mazzeo, Girolama Alessandra, Marfia, Andrea, Cortese, Brigida, Fierro, Stefano, Jann, Ettore, Beghi, Angelo Maurizio, Clerici, Marinella, Carpo, Angelo, Schenone, Marco, Luigetti, Giuseppe, Lauria, Giovanni, Antonini, Tiziana, Rosso, Gabriele, Siciliano, Guido, Cavaletti, Giuseppe, Liberatore, Lucio, Santoro, Erdita, Peci, Stefano, Tronci, Marta, Ruiz, Stefano, Cotti Piccinelli, Antonio, Toscano, Giorgia, Mataluni, Laura, Piccolo, Giuseppe, Cosentino, Mario, Sabatelli, Eduardo, Nobile-Orazio, Claudia, Balducci, Doneddu, P, Cocito, D, Manganelli, F, Fazio, R, Briani, C, Filosto, M, Benedetti, L, Mazzeo, A, Marfia, G, Cortese, A, Fierro, B, Jann, S, Beghi, E, Clerici, A, Carpo, M, Schenone, A, Luigetti, M, Lauria, G, Antonini, G, Rosso, T, Siciliano, G, Cavaletti, G, Liberatore, G, Santoro, L, Peci, E, Tronci, S, Ruiz, M, Cotti Piccinelli, S, Toscano, A, Mataluni, G, Piccolo, L, Cosentino, G, Sabatelli, M, Nobile-Orazio, E, Doneddu, Pietro Emiliano, Cocito, Dario, Manganelli, Fiore, Fazio, Raffaella, Briani, Chiara, Filosto, Massimiliano, Benedetti, Luana, Mazzeo, Anna, Marfia, Girolama Alessandra, Cortese, Andrea, Fierro, Brigida, Jann, Stefano, Beghi, Ettore, Clerici, Angelo Maurizio, Carpo, Marinella, Schenone, Angelo, Luigetti, Marco, Lauria, Giuseppe, Antonini, Giovanni, Rosso, Tiziana, Siciliano, Gabriele, Cavaletti, Guido, Liberatore, Giuseppe, Santoro, Lucio, Peci, Erdita, Tronci, Stefano, Ruiz, Marta, Cotti Piccinelli, Stefano, Toscano, Antonio, Mataluni, Giorgia, Piccolo, Laura, Cosentino, Giuseppe, Sabatelli, Mario, and Nobile-Orazio, Eduardo
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Adult ,Male ,Treatment response ,lewis-sumner syndrome ,Adolescent ,Databases, Factual ,Disease duration ,chronic inflammatory demyelinating polyradiculoneuropathy ,CIDP ,diagnostic criteria ,distal acquired demyelinating symmetric neuropathy ,Surgery ,Neurology (clinical) ,Psychiatry and Mental Health ,Kaplan-Meier Estimate ,computer.software_genre ,Disease course ,Young Adult ,lewis–sumner syndrome ,03 medical and health sciences ,0302 clinical medicine ,Humans ,Medicine ,In patient ,Child ,Aged ,Retrospective Studies ,Aged, 80 and over ,Retrospective review ,Database ,business.industry ,Polyradiculoneuropathy ,Middle Aged ,medicine.disease ,Psychiatry and Mental health ,surgery ,neurology ,psychiatry and mental health ,Italy ,Polyradiculoneuropathy, Chronic Inflammatory Demyelinating ,Disease Progression ,Female ,Settore MED/26 - Neurologia ,Progression rate ,business ,computer ,030217 neurology & neurosurgery - Abstract
ObjectivesA few variants of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) have been described, but their frequency and evolution to typical CIDP remain unclear. To determine the frequency and characteristics of the CIDP variants, their possible evolution to typical CIDP, and treatment response.MethodsWe applied a set of diagnostic criteria to 460 patients included in a database of Italian patients with CIDP. Clinical characteristics and treatment response were reviewed for each patient. The Kaplan-Meier curve was used to estimate the progression rate from atypical to typical CIDP.ResultsAt the time of inclusion, 376 (82%) patients had a diagnosis of typical CIDP while 84 (18%) had atypical CIDP, including 34 (7%) with distal acquired demyelinating symmetric neuropathy (DADS), 17 (4%) with purely motor, 17 (4%) with Lewis-Sumner syndrome (LSS) and 16 (3.5%) with purely sensory CIDP. Based on retrospective review of the symptoms and signs present at onset and for at least 1 year, 180 (39%) patients had an initial diagnosis compatible with atypical CIDP that in 96 (53%) patients evolved to typical CIDP. Mean disease duration was longer in patients evolving to typical CIDP than in those not evolving (p=0.0016). Patients with DADS and LSS had a less frequent response to immunoglobulin than those with typical CIDP, while patients with purely motor and sensory CIDP had a similar treatment response.ConclusionsThe proportion of patients with atypical CIDP varies during the disease course. DADS and LSS have a less frequent response to intravenous immunoglobulin compared with typical CIDP, raising the possibility of a different underlying pathogenetic mechanism.
- Published
- 2018
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