Search Results - "G. De Michele"

Metabolic effects of a diet with inulin-enriched pasta in healthy young volunteers by Russo, F, Riezzo, G, Chiloiro, M, De Michele, G, Chimienti, G, Marconi, E, D'Attoma, B, Linsalata, M, Clemente, C

“…Different lines of evidence suggest that higher intake of fiber may somehow protect against metabolic syndrome. The prebiotic inulin has widely been studied in…”
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Insulin-like growth factor-1 predicts cognitive functions at 2-year follow-up in early, drug-naïve Parkinson's disease by Pellecchia, M. T., Santangelo, G., Picillo, M., Pivonello, R., Longo, K., Pivonello, C., Vitale, C., Amboni, M., De Rosa, A., Moccia, M., Erro, R., De Michele, G., Santoro, L., Colao, A., Barone, P.

“…Background and purpose Cognitive impairment is common in Parkinson's disease (PD), even in the early stages. We aimed to assess the relationship between…”
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Static Magnetic Fields Effects on Polysaccharides Production by Different Microalgae Strains by Deamici, Kricelle M., de Morais, Michele G., Santos, Lucielen O., Muylaert, Koenraad, Gardarin, Christine, Costa, Jorge Alberto V., Laroche, Céline

“…Microalgae are able to produce many valuable biomolecules, such as polysaccharides, that presents a large diversity of biochemical structures and functions as…”
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Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism by Piccoli, C, Ripoli, M, Quarato, G, Scrima, R, D'Aprile, A, Boffoli, D, Margaglione, M, Criscuolo, C, De Michele, G, Sardanelli, A, Papa, S, Capitanio, N

“…Various genes have been identified for monogenic disorders resembling Parkinson's disease. The products of some of these genes are associated with mitochondria…”
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Low-dose idebenone treatment in Friedreich’s ataxia with and without cardiac hypertrophy by Rinaldi, C., Tucci, T., Maione, S., Giunta, A., De Michele, G., Filla, A.

“…Left ventricular hypertrophy (LVH) is a frequent finding in Friedreich’s ataxia (FRDA). In previous studies treatment with idebenone, a synthetic analogue of…”
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The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families by Lieto, M., Riso, V., Galatolo, D., De Michele, G., Rossi, S., Barghigiani, M., Cocozza, S., Pontillo, G., Trovato, R., Saccà, F., Salvatore, E., Tessa, A., Filla, A., Santorelli, F. M., De Michele, G., Silvestri, G.

“…Background and purpose Heterozygous mutations in the STUB1 gene have recently been associated with an autosomal dominant form of spinocerebellar ataxia (SCA)…”
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Relationship between apathy and cognitive dysfunctions in de novo untreated Parkinson's disease: a prospective longitudinal study by Santangelo, G., Vitale, C., Trojano, L., Picillo, M., Moccia, M., Pisano, G., Pezzella, D., Cuoco, S., Erro, R., Longo, K., Pellecchia, M. T., Amboni, M., De Rosa, A., De Michele, G., Barone, P.

“…Background and purpose Apathy may be either a symptom of major depression or a behavioral disturbance occurring in concomitance with depression or alone in…”
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Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay by Criscuolo, Chiara, Procaccini, C., Meschini, M. C., Cianflone, A., Carbone, R., Doccini, S., Devos, D., Nesti, C., Vuillaume, I., Pellegrino, M., Filla, A., De Michele, G., Matarese, G., Santorelli, F. M.

“…Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disease due to mutations in SACS, which encodes sacsin, a protein…”
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Mild cognitive impairment in drug-naive patients with PD is associated with cerebral hypometabolism by PAPPATA, S, SANTANGELO, G, PELLECCHIA, M. T, BRUNETTI, A, DE MICHELE, G, SALVATORE, M, BARONE, P, AARSLAND, D, VICIDOMINI, C, LONGO, K, BRONNICK, K, AMBONI, M, ERRO, R, VITALE, C, CAPRIO, M. G

“…To characterize brain metabolic changes associated with mild cognitive impairment (MCI) in drug-naive patients with Parkinson disease (PD) using…”
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Prevalence and phenotype of the c.1529C>T SPG7 variant in adult‐onset cerebellar ataxia in Italy by Mancini, C., Giorgio, E., Rubegni, A., Pradotto, L., Bagnoli, S., Rubino, E., Prontera, P., Cavalieri, S., Di Gregorio, E., Ferrero, M., Pozzi, E., Riberi, E., Ferrero, P., Nigro, P., Mauro, A., Zibetti, M., Tessa, A., Barghigiani, M., Antenora, A., Sirchia, F., Piacentini, S., Silvestri, G., De Michele, G., Filla, A., Orsi, L., Santorelli, F. M., Brusco, A.

“…Background and purpose Hereditary ataxias are heterogeneous groups of neurodegenerative disorders, characterized by cerebellar syndromes associated with…”
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Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich’s ataxia by Santoro, L, De Michele, G, Perretti, A, Crisci, C, Cocozza, S, Cavalcanti, F, Ragno, M, Monticelli, A, Filla, A, Caruso, G

“…OBJECTIVE To verify if GAA expansion size in Friedreich’s ataxia could account for the severity of sensory neuropathy. METHODS Retrospective study of 56…”
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60. The effect of cerebellar degeneration on human sensori-motor plasticity by Dubbioso, R, Pellegrino, G, Antenora, A, De Michele, G, Filla, A, Santoro, L, Manganelli, F

“…We investigated how cerebellar degeneration influences the plasticity of the tprimary motor cortex (M1) by using PAS (paired associative plasticity) technique…”
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Intrafamilial phenotypic variability in Spinocerebellar ataxia type 8 by Antenora, A, Peluso, S, Esposito, M, De Rosa, A, Brusco, A, Filla, A, De Michele, G

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Cognitive assessment in multiple system atrophy cerebellar type by Lieto, M, Saccà, F, Costabile, T, Antenora, A, Abate, F, Liguori, A, De Michele, G, Filla, A

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Brain structural damage in Friedreich’s ataxia by Nave, R Della, Ginestroni, A, Giannelli, M, Tessa, C, Salvatore, E, Salvi, F, Dotti, M T, De Michele, G, Piacentini, S, Mascalchi, M

“…Objective:Neuropathological descriptions of the brain in Friedreich’s ataxia (FRDA) were obtained before availability of the current molecular genetic tests…”
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Ataxia with oculomotor apraxia type 2 : A clinical, pathologic, and genetic study by CRISCUOLO, C, CHESSA, L, PIERELLI, F, RIZZUTO, N, SANTORELLI, F. M, GALLOSTI, L, FILLA, A, CASALI, C, DI GIANDOMENICO, S, MANCINI, P, SACCA, F, GRIECO, G. S, PIANE, M, BARBIERI, F, DE MICHELE, G, BANFI, S

“…Ataxia with oculomotor apraxia type 2 (AOA2) is characterized by onset between age 10 and 22 years, cerebellar atrophy, peripheral neuropathy, oculomotor…”
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Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism by De Rosa, A, Pellegrino, T, Pappatà, S, Lieto, M, Bonifati, V, Palma, V, Topa, A, Santoro, L, Bilo, L, Cuocolo, A, De Michele, G

“…Abstract Introduction PARK20 is a rare autosomal recessive parkinsonism related to the SYNJ1 gene and characterized by early-onset of disease and atypical…”
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Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families by Filla, A, Mariotti, C, Caruso, G, Coppola, G, Cocozza, S, Castaldo, I, Calabrese, O, Salvatore, E, De Michele, G, Riggio, M C, Pareyson, D, Gellera, C, Di Donato, S

“…Two hundred and forty-eight patients from 116 Italian families with dominant ataxia were studied for CAG expansion within SCA1, 2, 3, 6, 7 (spinocerebellar…”
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Spinocerebellar ataxia type 2 in southern Italy : a clinical and molecular study of 30 families by FILLA, A, DE MICHELE, G, SCALA, R, COPPOLA, G, CARUSO, G, COCOZZA, S, SANTORO, L, CALABRESE, O, CASTALDO, I, GIUFFRIDA, S, RESTIVO, D, SERLENGA, L, CONDORELLI, D. F, BONUCCELLI, U

“…Autosomal dominant cerebellar ataxia type I is the most common form of dominant ataxia. A genetic heterogeneity has been identified with five different loci…”
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SPG5 and multiple sclerosis: clinical and genetic overlap? by Criscuolo, C., Carbone, R., Lieto, M., Peluso, S., Guacci, A., Filla, A., Quarantelli, M., Lanzillo, R., Brescia Morra, V., De Michele, G.

“…Background Autosomal recessive (AR) spastic paraplegia type 5 (SPG5) is due to mutations in the CYP7B1 gene, encoding for the cytochrome P450‐7B1, responsible…”
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