Nonmotor Symptoms in Dopa‐Responsive Dystonia

di Antelmi, Elena, Stamelou, Maria, Liguori, Rocco, Bhatia, Kailash P.
Pubblicato in Mov Disord Clin Pract (2015)

Reviewing the Clinical Implications of Treating Narcolepsy as an Autoimmune Disorder

di Giannoccaro, Maria Pia, Liguori, Rocco, Plazzi, Giuseppe, Pizza, Fabio
Pubblicato in Nat Sci Sleep (2021)

Pain Related Channels Are Differentially Expressed in Neuronal and Non-Neuronal Cells of Glabrous Skin of Fabry Knockout Male Mice

di Lakomá, Jarmila, Rimondini, Roberto, Donadio, Vincenzo, Liguori, Rocco, Caprini, Marco
Pubblicazione 2014

Movement Disorders Associated with GABA(A) Receptor Encephalitis: A Video Case Report

di Vacchiano, Veria, Giannoccaro, Maria Pia, Rinaldi, Rita, Guarino, Maria, Liguori, Rocco
Pubblicato in Mov Disord Clin Pract (2020)

The autonomic innervation of hairy skin in humans: an in vivo confocal study

di Donadio, Vincenzo, Incensi, Alex, Vacchiano, Veria, Infante, Rossella, Magnani, Martina, Liguori, Rocco
Pubblicato in Sci Rep (2019)

Benefit and danger from immunotherapy in myasthenia gravis

di Rodolico, Carmelo, Nicocia, Giulia, Damato, Valentina, Antonini, Giovanni, Liguori, Rocco, Evoli, Amelia
Pubblicato in Neurol Sci (2021)

Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model

di Lakomá, Jarmila, Rimondini, Roberto, Ferrer Montiel, Antonio, Donadio, Vincenzo, Liguori, Rocco, Caprini, Marco
Pubblicato in Mol Pain (2016)

Primary progressive narcolepsy type 1: The other side of the coin

di Pizza, Fabio, Vandi, Stefano, Liguori, Rocco, Parchi, Piero, Avoni, Patrizia, Mignot, Emmanuel, Plazzi, Giuseppe
Pubblicato in Neurology (2014)

Nocturnal Sleep Dynamics Identify Narcolepsy Type 1

di Pizza, Fabio, Vandi, Stefano, Iloti, Martina, Franceschini, Christian, Liguori, Rocco, Mignot, Emmanuel, Plazzi, Giuseppe
Pubblicato in Sleep (2015)

Neurofilaments in motor neuron disorders: towards promising diagnostic and prognostic biomarkers

di Zucchi, Elisabetta, Bonetto, Valentina, Sorarù, Gianni, Martinelli, Ilaria, Parchi, Piero, Liguori, Rocco, Mandrioli, Jessica
Pubblicato in Mol Neurodegener (2020)

A Defective SERCA1 Protein Is Responsible for Congenital Pseudomyotonia in Chianina Cattle

di Sacchetto, Roberta, Testoni, Stefania, Gentile, Arcangelo, Damiani, Ernesto, Rossi, Marco, Liguori, Rocco, Drögemüller, Cord, Mascarello, Francesco
Pubblicazione 2009

Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations

di Murgiano, Leonardo, Sacchetto, Roberta, Testoni, Stefania, Dorotea, Tiziano, Mascarello, Francesco, Liguori, Rocco, Gentile, Arcangelo, Drögemüller, Cord
Pubblicazione 2012

Remitting Tics and Narcolepsy Overlap Associated with Streptococcal Infection: A Case Report

di Baiardi, Simone, Antelmi, Elena, Filardi, Marco, Pizza, Fabio, Vandi, Stefano, Veggiotti, Pierangelo, Liguori, Rocco, Plazzi, Giuseppe
Pubblicato in Mov Disord Clin Pract (2014)

First TMEM126A missense mutation in an Italian proband with optic atrophy and deafness

di La Morgia, Chiara, Caporali, Leonardo, Tagliavini, Francesca, Palombo, Flavia, Carbonelli, Michele, Liguori, Rocco, Barboni, Piero, Carelli, Valerio
Pubblicato in Neurol Genet (2019)

A 36‐Year‐Old Woman With Right Eye Ptosis

di Foschi, Matteo, Rizzo, Giovanni, Zoli, Matteo, Mazzatenta, Diego, Marliani, Frederica, Foschini, Maria Pia, Avoni, Patrizia, Liguori, Rocco
Pubblicato in Brain Pathol (2019)

Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases

di Foschi, Matteo, Vacchiano, Veria, Avoni, Patrizia, Incensi, Alex, Battaglia, Stella, Donadio, Vincenzo, Panzeri, Elena, Bassi, Maria Teresa, Liguori, Rocco, Rizzo, Giovanni
Pubblicato in Front Neurol (2019)

A case report of IgG4-related disease: an insidious path to the diagnosis through kidney, heart and brain

di Comai, Giorgia, Cuna, Vania, Fabbrizio, Benedetta, Sabattini, Elena, Leone, Ornella, Tondolo, Francesco, Angeletti, Andrea, Cappuccilli, Maria, Liguori, Rocco, La Manna, Gaetano
Pubblicato in BMC Nephrol (2019)

A Novel Null Homozygous Mutation Confirms CACNA2D2 as a Gene Mutated in Epileptic Encephalopathy

di Pippucci, Tommaso, Parmeggiani, Antonia, Palombo, Flavia, Maresca, Alessandra, Angius, Andrea, Crisponi, Laura, Cucca, Francesco, Liguori, Rocco, Valentino, Maria Lucia, Seri, Marco, Carelli, Valerio
Pubblicazione 2013

Color Choice Preference in Cognitively Impaired Patients: A Look Inside Alzheimer’s Disease Through the Use of Lüscher Color Diagnostic

di Stanzani Maserati, Michelangelo, Mitolo, Micaela, Medici, Federica, D’Onofrio, Renato, Oppi, Federico, Poda, Roberto, De Matteis, Maddalena, Tonon, Caterina, Lodi, Raffaele, Liguori, Rocco, Capellari, Sabina
Pubblicato in Front Psychol (2019)

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

di 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
Pubblicato in Autophagy (2018)