Modoni, Anna
COVID-19 atypical Parsonage-Turner syndrome: a case report
2022 Zazzara, M. B.; Modoni, A.; Bizzarro, A.; Lauria, A.; Ciciarello, F.; Pais, C.; Galluzzo, V.; Landi, F.; Tostato, M.
Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1)
2022 Nicoletti, Tommaso F; Rossi, Salvatore; Vita, Maria Gabriella; Perna, Alessia; Guerrera, Gisella; Lino, Federica; Iacovelli, Chiara; Di Natale, Daniele; Modoni, Anna; Battistini, Luca; Silvestri, Gabriella
Neurophysiological challenges in myasthenia gravis associated with MuSK antibodies: a case report
2022 Monte, G.; Evoli, A.; Sanders, D. B.; Modoni, A.
A man with sarcoidosis and slurred speech
2020 Nicoletti, T; Gaudino, S; Colacicco, G; Ausili Cefaro, L; Tasca, G; Guglielmi, V; Modoni, A; Gessi, M; Silvestri, G; Frisullo, G
Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia
2020 Santoro, M.; Perna, A.; La Rosa, P.; Petrillo, S.; Piemonte, F.; Rossi, S.; Riso, V.; Nicoletti, T. F.; Modoni, A.; Pomponi, M. G.; Chiurazzi, P.; Silvestri, G.
High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study
2020 Perna, A.; Maccora, D.; Rossi, S.; Nicoletti, T. F.; Zocco, M. A.; Riso, V.; Modoni, A.; Petrucci, A.; Valenza, V.; Grieco, A.; Miele, L.; Silvestri, G.
Progressive multifocal leukoencephalopathy in patients with follicular lymphoma treated with bendamustine plus rituximab followed by rituximab maintenance
2020 D'Alo', F.; Malafronte, R.; Piludu, F.; Bellesi, S.; Cuccaro, A.; Maiolo, E.; Modoni, A.; Leccisotti, L.; Macis, G.; Mores, N.; De Stefano, V.; Hohaus, S.
Progressive multifocal leukoencephalopathy in patients with follicular lymphoma treated with bendamustine plus rituximab followed by rituximab maintenance
2020 D'Alo, F.; Malafronte, R.; Piludu, F.; Bellesi, S.; Cuccaro, A.; Maiolo, E.; Modoni, A.; Leccisotti, L.; Macis, G.; Mores, N.; De Stefano, V.; Hohaus, S.
Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype"
2020 Rossi, Salvatore; Perna, Alessia; Modoni, Anna; Bertini, Enrico; Riso, Vittorio; Nicoletti, Tommaso Filippo; Silvestri, Gabriella
Resveratrol corrects aberrant splicing of RYR1 pre-mRNA and Ca2+ signal in myotonic dystrophy type 1 myotubes
2020 Santoro, M.; Piacentini, R.; Perna, A.; Pisano, E.; Severino, A.; Modoni, A.; Grassi, C.; Silvestri, G.
A Late Onset of Wernicke-Korsakoff Encephalopathy After Biliopancreatic Diversion: a Case Report
2019 Negri, M.; Macerola, N.; Mancarella, F. A.; Bruno, C.; De Leva, F.; D'Argento, F.; Pontecorvi, A.; Modoni, A.; Tartaglione, L.; Di Leo, M.; Pitocco, D.
Muscle hypertrophy in amyloid myopathy
2019 Tasca, G.; Modoni, A.; Nicoletti, T.; Monforte, M.; Cuccaro, A.; Ricci, E.
Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2
2018 Rossi, Salvatore; Romano, Angela; Modoni, Anna; Perna, Francesco; Rizzo, Valentina; Santoro, Massimo; Monforte, Mauro; Pieroni, Maurizio; Luigetti, Marco; Pomponi, Maria Grazia; Silvestri, Gabriella
Secondary hypokalemic periodic paralysis as a rare clinical presentation of Conn syndrome
2018 Nicoletti, T.; Modoni, A.; Silvestri, G.
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia
2018 Perna, A.; Masciullo, M.; Modoni, A.; Cellini, E.; Parrini, E.; Ricci, E.; Donati, A. M.; Silvestri, G.
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia
2017 Hasan, S.; Bove, C.; Silvestri, G.; Mantuano, E.; Modoni, A.; Veneziano, L.; Macchioni, L.; Hunter, T.; Hunter, G.; Pessia, M.; D'Adamo, M. C.
Serial neuroimaging findings in a novel case of sporadic progressive ataxia and palatal tremor (PAPT)
2017 Di Blasi, Chiara; Rizzo, Valentina; Di Lella, Giuseppe Maria; Modoni, Anna; Calcagni, Maria Lucia; Picciotti, Pasqualina Maria; Silvestri, Gabriella
An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy.
2016 Vanacore, N; Rastelli, E; Antonini, G; Bianchi, Maria Laura Ester; Botta, A; Bucci, E; Casali, C; Costanzi Porrini, S; Giacanelli, M; Gibellini, M; Modoni, Anna; Novelli, Giuseppe; Pennisi, Em; Petrucci, A; Piantadosi, C; Silvestri, Gabriella; Terracciano, C; Massa, R.
An atypical case of acute disseminated encephalomyelitis associated with cytomegalovirus infection
2016 De Fino, Chiara; Nociti, Viviana; Modoni, Anna; Bizzarro, Alessandra; Mirabella, Massimiliano
DJ-1 modulates mitochondrial response to oxidative stress: Clues from a novel diagnosis of PARK7
2016 Di Nottia, M.; Masciullo, M.; Verrigni, D.; Petrillo, S.; Modoni, Anna; Rizzo, Valentina; Di Giuda, Daniela; Rizza, T.; Niceta, M.; Torraco, A.; Bianchi, M.; Santoro, M.; Bentivoglio, Anna Rita; Bertini, Enrico Silvio; Piemonte, F.; Carrozzo, R; Silvestri, Gabriella
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
1-gen-2022 | COVID-19 atypical Parsonage-Turner syndrome: a case report | Zazzara, M. B.; Modoni, A.; Bizzarro, A.; Lauria, A.; Ciciarello, F.; Pais, C.; Galluzzo, V.; Landi, F.; Tostato, M. | |
1-gen-2022 | Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1) | Nicoletti, Tommaso F; Rossi, Salvatore; Vita, Maria Gabriella; Perna, Alessia; Guerrera, Gisella; Lino, Federica; Iacovelli, Chiara; Di Natale, Daniele; Modoni, Anna; Battistini, Luca; Silvestri, Gabriella | |
1-gen-2022 | Neurophysiological challenges in myasthenia gravis associated with MuSK antibodies: a case report | Monte, G.; Evoli, A.; Sanders, D. B.; Modoni, A. | |
1-gen-2020 | A man with sarcoidosis and slurred speech | Nicoletti, T; Gaudino, S; Colacicco, G; Ausili Cefaro, L; Tasca, G; Guglielmi, V; Modoni, A; Gessi, M; Silvestri, G; Frisullo, G | |
1-gen-2020 | Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia | Santoro, M.; Perna, A.; La Rosa, P.; Petrillo, S.; Piemonte, F.; Rossi, S.; Riso, V.; Nicoletti, T. F.; Modoni, A.; Pomponi, M. G.; Chiurazzi, P.; Silvestri, G. | |
1-gen-2020 | High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study | Perna, A.; Maccora, D.; Rossi, S.; Nicoletti, T. F.; Zocco, M. A.; Riso, V.; Modoni, A.; Petrucci, A.; Valenza, V.; Grieco, A.; Miele, L.; Silvestri, G. | |
1-gen-2020 | Progressive multifocal leukoencephalopathy in patients with follicular lymphoma treated with bendamustine plus rituximab followed by rituximab maintenance | D'Alo', F.; Malafronte, R.; Piludu, F.; Bellesi, S.; Cuccaro, A.; Maiolo, E.; Modoni, A.; Leccisotti, L.; Macis, G.; Mores, N.; De Stefano, V.; Hohaus, S. | |
1-gen-2020 | Progressive multifocal leukoencephalopathy in patients with follicular lymphoma treated with bendamustine plus rituximab followed by rituximab maintenance | D'Alo, F.; Malafronte, R.; Piludu, F.; Bellesi, S.; Cuccaro, A.; Maiolo, E.; Modoni, A.; Leccisotti, L.; Macis, G.; Mores, N.; De Stefano, V.; Hohaus, S. | |
1-gen-2020 | Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype" | Rossi, Salvatore; Perna, Alessia; Modoni, Anna; Bertini, Enrico; Riso, Vittorio; Nicoletti, Tommaso Filippo; Silvestri, Gabriella | |
1-gen-2020 | Resveratrol corrects aberrant splicing of RYR1 pre-mRNA and Ca2+ signal in myotonic dystrophy type 1 myotubes | Santoro, M.; Piacentini, R.; Perna, A.; Pisano, E.; Severino, A.; Modoni, A.; Grassi, C.; Silvestri, G. | |
1-gen-2019 | A Late Onset of Wernicke-Korsakoff Encephalopathy After Biliopancreatic Diversion: a Case Report | Negri, M.; Macerola, N.; Mancarella, F. A.; Bruno, C.; De Leva, F.; D'Argento, F.; Pontecorvi, A.; Modoni, A.; Tartaglione, L.; Di Leo, M.; Pitocco, D. | |
1-gen-2019 | Muscle hypertrophy in amyloid myopathy | Tasca, G.; Modoni, A.; Nicoletti, T.; Monforte, M.; Cuccaro, A.; Ricci, E. | |
1-gen-2018 | Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2 | Rossi, Salvatore; Romano, Angela; Modoni, Anna; Perna, Francesco; Rizzo, Valentina; Santoro, Massimo; Monforte, Mauro; Pieroni, Maurizio; Luigetti, Marco; Pomponi, Maria Grazia; Silvestri, Gabriella | |
1-gen-2018 | Secondary hypokalemic periodic paralysis as a rare clinical presentation of Conn syndrome | Nicoletti, T.; Modoni, A.; Silvestri, G. | |
1-gen-2018 | Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia | Perna, A.; Masciullo, M.; Modoni, A.; Cellini, E.; Parrini, E.; Ricci, E.; Donati, A. M.; Silvestri, G. | |
1-gen-2017 | A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia | Hasan, S.; Bove, C.; Silvestri, G.; Mantuano, E.; Modoni, A.; Veneziano, L.; Macchioni, L.; Hunter, T.; Hunter, G.; Pessia, M.; D'Adamo, M. C. | |
1-gen-2017 | Serial neuroimaging findings in a novel case of sporadic progressive ataxia and palatal tremor (PAPT) | Di Blasi, Chiara; Rizzo, Valentina; Di Lella, Giuseppe Maria; Modoni, Anna; Calcagni, Maria Lucia; Picciotti, Pasqualina Maria; Silvestri, Gabriella | |
1-gen-2016 | An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy. | Vanacore, N; Rastelli, E; Antonini, G; Bianchi, Maria Laura Ester; Botta, A; Bucci, E; Casali, C; Costanzi Porrini, S; Giacanelli, M; Gibellini, M; Modoni, Anna; Novelli, Giuseppe; Pennisi, Em; Petrucci, A; Piantadosi, C; Silvestri, Gabriella; Terracciano, C; Massa, R. | |
1-gen-2016 | An atypical case of acute disseminated encephalomyelitis associated with cytomegalovirus infection | De Fino, Chiara; Nociti, Viviana; Modoni, Anna; Bizzarro, Alessandra; Mirabella, Massimiliano | |
1-gen-2016 | DJ-1 modulates mitochondrial response to oxidative stress: Clues from a novel diagnosis of PARK7 | Di Nottia, M.; Masciullo, M.; Verrigni, D.; Petrillo, S.; Modoni, Anna; Rizzo, Valentina; Di Giuda, Daniela; Rizza, T.; Niceta, M.; Torraco, A.; Bianchi, M.; Santoro, M.; Bentivoglio, Anna Rita; Bertini, Enrico Silvio; Piemonte, F.; Carrozzo, R; Silvestri, Gabriella |