IRIS

MANGANELLI, FIORE

MANGANELLI, FIORE  

DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE  

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Titolo Tipologia Data di pubblicazione Autore(i) File
Ross syndrome: a rare or a misknown disorder of thermoregulation? A skin innervation study on 12 subjects. 1.1 Articolo in rivista 2006 Nolano, M; Provitera, V; Perretti, A; Stancanelli, A; Saltalamacchia, Am; Donadio, V; Manganelli, Fiore; Lanzillo, B; Santoro, Lucio
Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease). 1.1 Articolo in rivista 2007 Manganelli, Fiore; Iodice, V; Provitera, V; Pisciotta, C; Nolano, M; Perretti, A; Santoro, Lucio
Inherited neuromyotonia: A clinical and genetic study of a family. 1.1 Articolo in rivista 2007 Falace, A; Striano, P; Manganelli, Fiore; Coppola, A; Striano, Salvatore; Minetti, C; Zara, F.; Coppola, Antonietta
Influence of GAA expansion size and disease duration on central nervous system impairment in Friedreich's ataxia: contribution to the understanding of the pathophysiology of the disease. 1.1 Articolo in rivista 2000 Santoro, Lucio; A., Perretti; B., Lanzillo; G., Coppola; G. D., Joanna; Manganelli, Fiore; Cocozza, Sergio; DE MICHELE, Giuseppe; Filla, Alessandro; G., Caruso
Case of acute motor conduction block neuropathy (AMCBN) 1.1 Articolo in rivista 2009 Manganelli, Fiore; Pisciotta, C; Iodice, Rosa; Calandro, S; Dubbioso, R; Ranieri, A; Santoro, Lucio; Dubbioso, Raffaele
Somatosensory Temporal Discrimination Threshold Is Increased in Patients with Cerebellar Atrophy. 1.1 Articolo in rivista 2013 Manganelli, Fiore; Dubbioso, Raffaele; Pisciotta, Chiara; Antenora, Antonella; Nolano, M; DE MICHELE, Giuseppe; Filla, Alessandro; Berardelli, A; Santoro, Lucio; Nolano, Maria
Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population 1.1 Articolo in rivista 2014 Manganelli, Fiore; Tozza, Stefano; Pisciotta, Chiara; Bellone, Emilia; Iodice, Rosa; Nolano, Maria; Geroldi, Alessandro; Capponi, Simona; Mandich, Paola; Santoro, Lucio; Nolano, Maria
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. 1.1 Articolo in rivista 2011 Santoro, Lucio; Breedveld, Gj; Manganelli, Fiore; Iodice, Rosa; Pisciotta, Chiara; Nolano, M; Punzo, F; Quarantelli, Mario; Pappatà, S; Di Fonzo, A; Oostra, Ba; Bonifati, V.
Post-exercise facilitation and depression of motor evoked potentials to transcranial magnetic stimulation: a study in multiple sclerosis 1.1 Articolo in rivista 2004 Perretti, ANNA CARMELA AGNESE; Balbi, P; Orefice, Giuseppe; Trojano, L; Marcantonio, L; BRESCIA MORRA, Vincenzo; Ascione, S; Manganelli, Fiore; Conte, G; Santoro, Lucio
Levetiracetam in patients with cortical myoclonus: a clinical and electrophysiological study. 1.1 Articolo in rivista 2005 Striano, P; Manganelli, Fiore; Boccella, P; Perretti, A; Striano, Salvatore
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL. 1.1 Articolo in rivista 2007 Bianchi, S; Dotti, Mt; Perretti, A; De Rosa, A; Manganelli, Fiore; Federico, A.
A Novel mutat of melin protein zero associated with an axonal form of Charcot-Marie.Tooth disease 1.1 Articolo in rivista 2004 Santoro, Lucio; Manganelli, Fiore; DI MARIA, E; Bordo, D; Cassandrini, D; Ajmar, F; Mandich, P; Bellone, E.
Trigeminal stimulation elicits a peripheral vestibular imbalance in migraine patients. 1.1 Articolo in rivista 2005 Marano, E; Marcelli, V; Di Stasio, E; Bonuso, S; Vacca, G; Manganelli, Fiore; Marciano, Elio; Perretti, A.
Distal hypoglycemic neuropathy. An insulinoma-associated case, misdiagnosed as temporal lobe epilepsy. 1.1 Articolo in rivista 2003 Striano, Salvatore; Striano, P; Manganelli, Fiore; Boccella, P; Bruno, R; Santoro, Lucio; Percopo, V.
A second family with hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibres, detected in the same geographic area as the first family. 1.1 Articolo in rivista 1998 Santoro, Lucio; Barbieri, Fabrizio; Crisci, C; Gasparo Rippa, P; Manganelli, Fiore
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 1.1 Articolo in rivista 2011 Manganelli, Fiore; Dubbioso, Raffaele; Nolano, M; Iodice, Rosa; Pisciotta, Chiara; Provitera, V; Ruggiero, Lucia; Serlenga, L; Barbieri, Fabrizio; Santoro, Lucio
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 1.1 Articolo in rivista 2006 Santoro, Lucio; Manganelli, Fiore; Lanzillo, Roberta; Tessa, A; Barbieri, Fabrizio; Pierelli, F; Di Giacinto, G; Nigro, V; Santorelli, F. M.
Two families with novel PMP22 point mutations: genotype-phenotype correlation. 1.1 Articolo in rivista 2009 Pisciotta, Chiara; Manganelli, Fiore; Iodice, Rosa; Bellone, E; Geroldi, A; Volpi, N; Mandich, P; Santoro, Lucio
Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family. 1.1 Articolo in rivista 2005 Ragno, M; Perretti, Ac; Castaldo, I; Scarcella, M; Acciarri, S; Manganelli, Fiore; Santoro, Lucio
Anti-GAD antibody ocular flutter: expanding the spectrum of autoimmune ocular motor disorders 1.1 Articolo in rivista 2013 Dubbioso, Raffaele; Vincenzo, Marcelli; Manganelli, Fiore; Iodice, Rosa; Esposito, Marcello; Santoro, Lucio