MANGANELLI, FIORE
MANGANELLI, FIORE
DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE
Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease).
2007 Manganelli, Fiore; Iodice, V; Provitera, V; Pisciotta, C; Nolano, M; Perretti, A; Santoro, Lucio
Case of acute motor conduction block neuropathy (AMCBN)
2009 Manganelli, Fiore; Pisciotta, C; Iodice, Rosa; Calandro, S; Dubbioso, R; Ranieri, A; Santoro, Lucio; Dubbioso, Raffaele
Inherited neuromyotonia: A clinical and genetic study of a family.
2007 Falace, A; Striano, P; Manganelli, Fiore; Coppola, A; Striano, Salvatore; Minetti, C; Zara, F.; Coppola, Antonietta
Reply (Acute motor conduction block neuropathy or acute multifocal motor neuropathy: an attempt at a nosological systematization)
2010 Manganelli, Fiore; Pisciotta, Chiara; Iodice, Rosa; Dubbioso, Raffaele; Santoro, Lucio
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.
1998 Santoro, Lucio; Barbieri, Fabrizio; Crisci, C; Gasparo Rippa, P; Manganelli, Fiore
Mutilating fingertip ulcers in uncontrolled type 1 diabetes mellitus.
2014 Dubbioso, Raffaele; Nolano, Maria; Mazzarella, Raffaella; Rivellese, ANGELA ALBAROSA; Manganelli, Fiore
Two families with novel PMP22 point mutations: genotype-phenotype correlation.
2009 Pisciotta, Chiara; Manganelli, Fiore; Iodice, Rosa; Bellone, E; Geroldi, A; Volpi, N; Mandich, P; Santoro, Lucio
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL.
2007 Bianchi, S; Dotti, Mt; Perretti, A; De Rosa, A; Manganelli, Fiore; Federico, A.
Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome.
2006 Santoro, Lucio; Manganelli, Fiore; Bruno, R; Nolano, M; Provitera, V; Barbieri, Fabrizio
Trigeminal stimulation elicits a peripheral vestibular imbalance in migraine patients.
2005 Marano, E; Marcelli, V; Di Stasio, E; Bonuso, S; Vacca, G; Manganelli, Fiore; Marciano, Elio; Perretti, A.
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family.
2002 Santoro, Lucio; Manganelli, Fiore; Di Maio, L; Barbieri, Fabrizio; Carella, M; D'Adamo, P; Casari, G.
Small fiber neuropathy in the chronic phase of Chagas disease: a case report
2013 Nolano, Maria; Provitera, Vincenzo; Manganelli, Fiore; A., Pagano; A., Perretti; Santoro, Lucio
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.
2000 Santoro, Lucio; A., Perretti; B., Lanzillo; G., Coppola; G. D., Joanna; Manganelli, Fiore; Cocozza, Sergio; DE MICHELE, Giuseppe; Filla, Alessandro; G., Caruso
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy
2011 Manganelli, Fiore; Dubbioso, Raffaele; Nolano, M; Iodice, Rosa; Pisciotta, Chiara; Provitera, V; Ruggiero, Lucia; Serlenga, L; Barbieri, Fabrizio; Santoro, Lucio
Somatosensory Temporal Discrimination Threshold Is Increased in Patients with Cerebellar Atrophy.
2013 Manganelli, Fiore; Dubbioso, Raffaele; Pisciotta, Chiara; Antenora, Antonella; Nolano, M; DE MICHELE, Giuseppe; Filla, Alessandro; Berardelli, A; Santoro, Lucio; Nolano, Maria
Central cholinergic dysfunction in the adult form of Niemann Pick disease type C: a further link with Alzheimer's disease?
2014 Manganelli, Fiore; Dubbioso, Raffaele; Iodice, Rosa; Topa, Antonietta; Dardis, A; Russo, Cv; Ruggiero, Lucia; Tozza, S; Filla, Alessandro; Santoro, Lucio
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features.
2006 Biancheri, R; Zara, F; Striano, P; Pedemonte, M; Cassandrini, D; Stringara, S; Manganelli, Fiore; Santoro, Lucio; Schenone, A; Bellone, E; Minetti, C.
A Novel mutat of melin protein zero associated with an axonal form of Charcot-Marie.Tooth disease
2004 Santoro, Lucio; Manganelli, Fiore; DI MARIA, E; Bordo, D; Cassandrini, D; Ajmar, F; Mandich, P; Bellone, E.
Levetiracetam in patients with cortical myoclonus: a clinical and electrophysiological study.
2005 Striano, P; Manganelli, Fiore; Boccella, P; Perretti, A; Striano, Salvatore
Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family.
2005 Ragno, M; Perretti, Ac; Castaldo, I; Scarcella, M; Acciarri, S; Manganelli, Fiore; Santoro, Lucio
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| 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 | |
| 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 | |
| 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 | |
| Reply (Acute motor conduction block neuropathy or acute multifocal motor neuropathy: an attempt at a nosological systematization) | 1.7 Commento, erratum, replica e simili | 2010 | Manganelli, Fiore; Pisciotta, Chiara; Iodice, Rosa; Dubbioso, Raffaele; Santoro, Lucio | |
| 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 | |
| Mutilating fingertip ulcers in uncontrolled type 1 diabetes mellitus. | 1.1 Articolo in rivista | 2014 | Dubbioso, Raffaele; Nolano, Maria; Mazzarella, Raffaella; Rivellese, ANGELA ALBAROSA; Manganelli, Fiore | |
| 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 | |
| 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. | |
| Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome. | 1.1 Articolo in rivista | 2006 | Santoro, Lucio; Manganelli, Fiore; Bruno, R; Nolano, M; Provitera, V; Barbieri, Fabrizio | |
| 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. | |
| Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. | 1.1 Articolo in rivista | 2002 | Santoro, Lucio; Manganelli, Fiore; Di Maio, L; Barbieri, Fabrizio; Carella, M; D'Adamo, P; Casari, G. | |
| Small fiber neuropathy in the chronic phase of Chagas disease: a case report | 1.1 Articolo in rivista | 2013 | Nolano, Maria; Provitera, Vincenzo; Manganelli, Fiore; A., Pagano; A., Perretti; Santoro, Lucio | |
| 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 | |
| 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 | |
| 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 | |
| Central cholinergic dysfunction in the adult form of Niemann Pick disease type C: a further link with Alzheimer's disease? | 1.1 Articolo in rivista | 2014 | Manganelli, Fiore; Dubbioso, Raffaele; Iodice, Rosa; Topa, Antonietta; Dardis, A; Russo, Cv; Ruggiero, Lucia; Tozza, S; Filla, Alessandro; Santoro, Lucio | |
| GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. | 1.1 Articolo in rivista | 2006 | Biancheri, R; Zara, F; Striano, P; Pedemonte, M; Cassandrini, D; Stringara, S; Manganelli, Fiore; Santoro, Lucio; Schenone, A; Bellone, E; Minetti, C. | |
| 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. | |
| 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 | |
| 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 |