Works by Scarlato, Marina

Results: 36

Muscle MRI findings in facioscapulohumeral muscular dystrophy.

Published in:

2016

By:

Gerevini, Simonetta;
Scarlato, Marina;
Maggi, Lorenzo;
Cava, Mariangela;
Caliendo, Giandomenico;
Pasanisi, Barbara;
Falini, Andrea;
Previtali, Stefano;
Morandi, Lucia;
Previtali, Stefano Carlo

Publication type:

journal article

Validation of a graphic test to quantitatively assess the dominant hand dexterity.

Published in:

PLoS ONE, 2022, v. 17, n. 8, p. 1, doi. 10.1371/journal.pone.0271889

By:

Angelucci, Alessandra;
Tettamanti, Andrea;
Sarasso, Elisabetta;
Filippi, Massimo;
Aliverti, Andrea;
Scarlato, Marina

Publication type:

Article

A fatal case of Churg-Strauss syndrome presenting with acute polyneuropathy mimicking Guillain-Barré syndrome.

Published in:

2011

By:

De Toni Franceschini L;
Amadio S;
Scarlato M;
Fazio R;
Quattrini A;
Dell'antonio G;
Comi G;
Del Carro U;
De Toni Franceschini, Luisa;
Amadio, Stefano;
Scarlato, Marina;
Fazio, Raffaella;
Quattrini, Angelo;
Dell'antonio, Giacomo;
Comi, Giancarlo;
Del Carro, Ubaldo

Publication type:

journal article

A fatal case of Churg-Strauss syndrome presenting with acute polyneuropathy mimicking Guillain-Barré syndrome.

Published in:

Neurological Sciences, 2011, v. 32, n. 5, p. 937, doi. 10.1007/s10072-011-0591-7

By:

Toni Franceschini, Luisa;
Amadio, Stefano;
Scarlato, Marina;
Fazio, Raffaella;
Quattrini, Angelo;
Dell'Antonio, Giacomo;
Comi, Giancarlo;
Carro, Ubaldo

Publication type:

Article

Subcutaneous immunoglobulin therapy for the treatment of multifocal motor neuropathy: a case report.

Published in:

Neurological Sciences, 2010, v. 31, n. 6, p. 829, doi. 10.1007/s10072-010-0352-z

By:

Dacci, Patrizia;
Riva, Nilo;
Scarlato, Marina;
Andresen, Irmgard;
Schmidt, DirkSteffen;
Comi, Giancarlo;
Fazio, Raffaella

Publication type:

Article

Loss of function MPZ mutation causes milder CMT1B neuropathy.

Published in:

Journal of the Peripheral Nervous System, 2021, v. 26, n. 2, p. 177, doi. 10.1111/jns.12452

By:

Howard, Paige;
Feely, Shawna M. E.;
Grider, Tiffany;
Bacha, Alexa;
Scarlato, Marina;
Fazio, Raffaella;
Quattrini, Angelo;
Shy, Michael E.;
Previtali, Stefano C.

Publication type:

Article

A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2.

Published in:

2015

By:

Scarlato, Marina;
Viganò, Fiammetta;
Carrera, Paola;
Previtali, Stefano Carlo;
Bolino, Alessandra

Publication type:

Letter to the Editor

Expanding the central nervous system disease spectrum associated with FLNC mutation.

Published in:

2019

By:

Previtali, Stefano C.;
Scarlato, Marina;
Vezzulli, Paolo;
Ruggieri, Alessandra;
Velardo, Daniele;
Benedetti, Sara;
Torini, Giacomo;
Colombo, Bruno;
Maggi, Lorenzo;
Di Bella, Daniela;
Gellera, Cinzia;
D'Angelo, Grazia;
Mora, Marina

Publication type:

journal article

Correction to: Daytime sleepiness and sleep quality in Charcot–Marie–Tooth disease.

Published in:

2023

By:

Bellofatto, Marta;
Gentile, Luca;
Bertini, Alessandro;
Tramacere, Irene;
Manganelli, Fiore;
Fabrizi, Gian Maria;
Schenone, Angelo;
Santoro, Lucio;
Cavallaro, Tiziana;
Grandis, Marina;
Previtali, Stefano C.;
Scarlato, Marina;
Allegri, Isabella;
Padua, Luca;
Pazzaglia, Costanza;
Villani, Flavio;
Cavalca, Eleonora;
Saveri, Paola;
Quattrone, Aldo;
Valentino, Paola

Publication type:

Correction Notice

Daytime sleepiness and sleep quality in Charcot–Marie–Tooth disease.

Published in:

Journal of Neurology, 2023, v. 270, n. 11, p. 5561, doi. 10.1007/s00415-023-11911-y

By:

Bellofatto, Marta;
Gentile, Luca;
Bertini, Alessandro;
Tramacere, Irene;
Manganelli, Fiore;
Fabrizi, Gian Maria;
Schenone, Angelo;
Santoro, Lucio;
Cavallaro, Tiziana;
Grandis, Marina;
Previtali, Stefano C.;
Scarlato, Marina;
Allegri, Isabella;
Padua, Luca;
Pazzaglia, Costanza;
Villani, Flavio;
Cavalca, Eleonora;
Saveri, Paola;
Quattrone, Aldo;
Valentino, Paola

Publication type:

Article

A 5-year clinical follow-up study from the Italian National Registry for FSHD.

Published in:

Journal of Neurology, 2021, v. 268, n. 1, p. 356, doi. 10.1007/s00415-020-10144-7

By:

Vercelli, Liliana;
Mele, Fabiano;
Ruggiero, Lucia;
Sera, Francesco;
Tripodi, Silvia;
Ricci, Giulia;
Vallarola, Antonio;
Villa, Luisa;
Govi, Monica;
Maranda, Louise;
Di Muzio, Antonio;
Scarlato, Marina;
Bucci, Elisabetta;
Maggi, Lorenzo;
Rodolico, Carmelo;
Moggio, Maurizio;
Filosto, Massimiliano;
Antonini, Giovanni;
Previtali, Stefano;
Angelini, Corrado

Publication type:

Article

Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.

Published in:

2017

By:

Scarlato, Marina;
Citterio, Andrea;
Barbieri, Alessandra;
Godi, Claudia;
Panzeri, Elena;
Bassi, Maria

Publication type:

Letter

A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation.

Published in:

2015

By:

Scarlato, Marina;
Nuara, Arturo;
Gerevini, Simonetta;
Benedetti, Sara;
Rossi, Paolo;
Ferrari, Maurizio;
Previtali, Stefano

Publication type:

Letter

Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy.

Published in:

JAMA Network Open, 2020, v. 3, n. 5, p. e204040, doi. 10.1001/jamanetworkopen.2020.4040

By:

Ruggiero, Lucia;
Mele, Fabiano;
Manganelli, Fiore;
Bruzzese, Dario;
Ricci, Giulia;
Vercelli, Liliana;
Govi, Monica;
Vallarola, Antonio;
Tripodi, Silvia;
Villa, Luisa;
Di Muzio, Antonio;
Scarlato, Marina;
Bucci, Elisabetta;
Antonini, Giovanni;
Maggi, Lorenzo;
Rodolico, Carmelo;
Tomelleri, Giuliano;
Filosto, Massimiliano;
Previtali, Stefano;
Angelini, Corrado

Publication type:

Article

Overcoming therapeutic challenges: Successful management of a supposedly triple seronegative, refractory generalized myasthenia gravis patient with efgartigimod.

Published in:

European Journal of Neurology, 2024, v. 31, n. 7, p. 1, doi. 10.1111/ene.16306

By:

Sorrenti, Benedetta;
Laurini, Christian;
Bosco, Luca;
Strano, Camilla Mirella Maria;
Scarlato, Marina;
Gastaldi, Matteo;
Filippi, Massimo;
Previtali, Stefano Carlo;
Falzone, Yuri Matteo

Publication type:

Article

Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis.

Published in:

Brain: A Journal of Neurology, 2005, v. 128, n. 8, p. 1911, doi. 10.1093/brain/awh519

By:

Marina Scarlato;
Stefano Carlo Previtali;
Marinella Carpo;
Davide Pareyson;
Chiara Briani;
Roberto Del Bo;
Eduardo Nobile-Orazio;
Angelo Quattrini;
Giacomo Pietro Comi

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 2005, v. 58, n. 3, p. 488

By:

Roberto Del Bo;
Marina Scarlato;
Filippo Martinelli Boneschi;
Serena Ghezzi;
Nereo Bresolin;
Giacomo P. Comi

Publication type:

Article

Vascular endothelial growth factor gene variability is associated with increased risk for AD.

Published in:

Annals of Neurology, 2005, v. 57, n. 3, p. 373

By:

Roberto Del Bo;
Marina Scarlato;
Serena Ghezzi;
Filippo Martinelli Boneschi;
Chiara Fenoglio;
Sara Galbiati;
Roberta Virgilio;
Daniela Galimberti;
Gloria Galimberti;
Marco Crimi;
Carlo Ferrarese;
Elio Scarpini;
Nereo Bresolin;
Giacomo P. Comi

Publication type:

Article

Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy.

Published in:

EMBO Molecular Medicine, 2016, v. 8, n. 12, p. 1470, doi. 10.15252/emmm.201607129

By:

Cossu, Giulio;
Previtali, Stefano C;
Napolitano, Sara;
Cicalese, Maria Pia;
Tedesco, Francesco Saverio;
Nicastro, Francesca;
Noviello, Maddalena;
Roostalu, Urmas;
Natali Sora, Maria Grazia;
Scarlato, Marina;
De Pellegrin, Maurizio;
Godi, Claudia;
Giuliani, Serena;
Ciotti, Francesca;
Tonlorenzi, Rossana;
Lorenzetti, Isabella;
Rivellini, Cristina;
Benedetti, Sara;
Gatti, Roberto;
Marktel, Sarah

Publication type:

Article

Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy.

Published in:

EMBO Molecular Medicine, 2015, v. 7, n. 12, p. 1513, doi. 10.15252/emmm.201505636

By:

Cossu, Giulio;
Previtali, Stefano C;
Napolitano, Sara;
Cicalese, Maria Pia;
Tedesco, Francesco Saverio;
Nicastro, Francesca;
Noviello, Maddalena;
Roostalu, Urmas;
Natali Sora, Maria Grazia;
Scarlato, Marina;
De Pellegrin, Maurizio;
Godi, Claudia;
Giuliani, Serena;
Ciotti, Francesca;
Tonlorenzi, Rossana;
Lorenzetti, Isabella;
Rivellini, Cristina;
Benedetti, Sara;
Gatti, Roberto;
Marktel, Sarah

Publication type:

Article

Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy.

Published in:

BMC Musculoskeletal Disorders, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12891-023-07150-x

By:

Bettio, Cinzia;
Banchelli, Federico;
Salsi, Valentina;
Vicini, Roberto;
Crisafulli, Oscar;
Ruggiero, Lucia;
Ricci, Giulia;
Bucci, Elisabetta;
Angelini, Corrado;
Berardinelli, Angela;
Bonanno, Silvia;
D'Angelo, Maria Grazia;
Di Muzio, Antonio;
Filosto, Massimiliano;
Frezza, Erica;
Maggi, Lorenzo;
Mongini, Tiziana;
Pegoraro, Elena;
Rodolico, Carmelo;
Scarlato, Marina

Publication type:

Article

ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis.

Published in:

Autophagy, 2019, v. 15, n. 1, p. 34, doi. 10.1080/15548627.2018.1507438

By:

Vantaggiato, Chiara;
Panzeri, Elena;
Castelli, Marianna;
Citterio, Andrea;
Arnoldi, Alessia;
Santorelli, Filippo Maria;
Liguori, Rocco;
Scarlato, Marina;
Musumeci, Olimpia;
Toscano, Antonio;
Clementi, Emilio;
Bassi, Maria Teresa

Publication type:

Article

Diffuse intraneural leiomyoma in a case of sensorimotor neuropathy.

Published in:

2009

By:

Cerri, Federica;
Gavazzi, Armando;
Previtali, Stefano;
Franceschi, Massimo;
Lopez, Ignazio D.;
Scarlato, Marina;
Podini, Paola;
Comi, Giancarlo;
Quattrini, Angelo

Publication type:

Letter

Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial.

Published in:

2017

By:

Schöls, Ludger;
Rattay, Tim W.;
Martus, Peter;
Meisner, Christoph;
Baets, Jonathan;
Fischer, Imma;
Jägle, Christine;
Fraidakis, Matthew J.;
Martinuzzi, Andrea;
Saute, Jonas Alex;
Scarlato, Marina;
Antenora, Antonella;
Stendel, Claudia;
Höflinger, Philip;
Lourenco, Charles Marques;
Abreu, Lisa;
Smets, Katrien;
Paucar, Martin;
Deconinck, Tine;
Bis, Dana M.

Publication type:

journal article

CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

Published in:

2015

By:

Ronchi, Dario;
Riboldi, Giulietta;
Del Bo, Roberto;
Ticozzi, Nicola;
Scarlato, Marina;
Galimberti, Daniela;
Corti, Stefania;
Silani, Vincenzo;
Bresolin, Nereo;
Comi, Giacomo Pietro

Publication type:

journal article

Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15.

Published in:

Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3119, doi. 10.1093/brain/awt227

By:

Vantaggiato, Chiara;
Crimella, Claudia;
Airoldi, Giovanni;
Polishchuk, Roman;
Bonato, Sara;
Brighina, Erika;
Scarlato, Marina;
Musumeci, Olimpia;
Toscano, Antonio;
Martinuzzi, Andrea;
Santorelli, Filippo Maria;
Ballabio, Andrea;
Bresolin, Nereo;
Clementi, Emilio;
Bassi, Maria Teresa

Publication type:

Article

Motor nerve biopsy: Clinical usefulness and histopathological criteria.

Published in:

Annals of Neurology, 2011, v. 69, n. 1, p. 197, doi. 10.1002/ana.22110

By:

Riva, Nilo;
Iannaccone, Sandro;
Corbo, Massimo;
Casellato, Chiara;
Sferrazza, Barbara;
Lazzerini, Alberto;
Scarlato, Marina;
Cerri, Federica;
Previtali, Stefano C.;
Nobile-Orazio, Eduardo;
Comi, Giancarlo;
Quattrini, Angelo

Publication type:

Article

Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy.

Published in:

Annals of Clinical & Translational Neurology, 2016, v. 3, n. 8, p. 607, doi. 10.1002/acn3.319

By:

Godi, Claudia;
Ambrosi, Alessandro;
Nicastro, Francesca;
Previtali, Stefano C.;
Santarosa, Corrado;
Napolitano, Sara;
Iadanza, Antonella;
Scarlato, Marina;
Natali Sora, Maria Grazia;
Tettamanti, Andrea;
Gerevini, Simonetta;
Cicalese, Maria Pia;
Sitzia, Clementina;
Venturini, Massimo;
Falini, Andrea;
Gatti, Roberto;
Ciceri, Fabio;
Cossu, Giulio;
Torrente, Yvan;
Politi, Letterio S.

Publication type:

Article

Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-78578-7

By:

Ricci, Giulia;
Mele, Fabiano;
Govi, Monica;
Ruggiero, Lucia;
Sera, Francesco;
Vercelli, Liliana;
Bettio, Cinzia;
Santoro, Lucio;
Mongini, Tiziana;
Villa, Luisa;
Moggio, Maurizio;
Filosto, Massimiliano;
Scarlato, Marina;
Previtali, Stefano C.;
Tripodi, Silvia Maria;
Pegoraro, Elena;
Telese, Roberta;
Di Muzio, Antonio;
Rodolico, Carmelo;
Bucci, Elisabetta

Publication type:

Article

Sodium Channel Myotonia Due to Novel Mutations in Domain I of Na<sub>v</sub>1.4.

Published in:

Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00255

By:

Pagliarani, Serena;
Lucchiari, Sabrina;
Scarlato, Marina;
Redaelli, Elisa;
Modoni, Anna;
Magri, Francesca;
Fossati, Barbara;
Previtali, Stefano C.;
Sansone, Valeria A.;
Lecchi, Marzia;
Lo Monaco, Mauro;
Meola, Giovanni;
Comi, Giacomo P.

Publication type:

Article

Sodium Channel Myotonia Due to Novel Mutations in Domain I of Na<sub>v</sub>1.4.

Published in:

Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00255

By:

Pagliarani, Serena;
Lucchiari, Sabrina;
Scarlato, Marina;
Redaelli, Elisa;
Modoni, Anna;
Magri, Francesca;
Fossati, Barbara;
Previtali, Stefano C.;
Sansone, Valeria A.;
Lecchi, Marzia;
Lo Monaco, Mauro;
Meola, Giovanni;
Comi, Giacomo P.

Publication type:

Article

Urokinase Plasminogen Receptor and the Fibrinolytic Complex Play a Role in Nerve Repair after Nerve Crush in Mice, and in Human Neuropathies.

Published in:

PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0032059

By:

Rivellini, Cristina;
Dina, Giorgia;
Porrello, Emanuela;
Cerri, Federica;
Scarlato, Marina;
Domi, Teuta;
Ungaro, Daniela;
Del Carro, Ubaldo;
Bolino, Alessandra;
Quattrini, Angelo;
Comi, Giancarlo;
Previtali, Stefano C.

Publication type:

Article

ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases.

Published in:

2015

By:

Magri, Francesca;
Colombo, Irene;
Bo, Roberto Del;
Previtali, Stefano;
Brusa, Roberta;
Ciscato, Patrizia;
Scarlato, Marina;
Ronchi, Dario;
D'Angelo, Maria Grazia;
Corti, Stefania;
Moggio, Maurizio;
Bresolin, Nereo;
Comi, Giacomo Pietro;
Del Bo, Roberto

Publication type:

journal article

Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures.

Published in:

BMC Neurology, 2012, v. 12, n. 1, p. 91, doi. 10.1186/1471-2377-12-91

By:

Lerario, Alberto;
Bonfiglio, Serena;
Sormani, MariaPia;
Tettamanti, Andrea;
Marktel, Sarah;
Napolitano, Sara;
Previtali, Stefano;
Scarlato, Marina;
Natali-Sora, MariaGrazia;
Mercuri, Eugenio;
Bresolin, Nereo;
Mongini, Tiziana;
Comi, Giancarlo;
Gatti, Roberto;
Ciceri, Fabio;
Cossu, Giulio;
Torrente, Yvan

Publication type:

Article

VEGF gene variability and type 1 diabetes: evidence for a protective role.

Published in:

Immunogenetics, 2006, v. 58, n. 2/3, p. 107, doi. 10.1007/s00251-006-0089-2

By:

Del Bo, Roberto;
Scarlato, Marina;
Ghezzi, Serena;
Maestroni, Anna;
Sjölind, Lisa;
Forsblom, Carol;
Wessman, Maija;
Groop, Per-Henrik;
Pietro Comi, Giacomo;
Bresolin, Nereo;
Luzi, Livio;
Zerbini, Gianpaolo

Publication type:

Article

Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias.

Published in:

Muscle & Nerve, 2011, v. 43, n. 2, p. 164, doi. 10.1002/mus.21872

By:

Briani, Chiara;
Fabrizi, Gian Maria;
Ruggero, Susanna;
Torre, Chiara Dalla;
Ferrarini, Moreno;
Campagnolo, Marta;
Cavallaro, Tiziana;
Ferrari, Sergio;
Scarlato, Marina;
Taioli, Federica;
Adami, Fausto

Publication type:

Article