G De Michele
Overview
Explore the profile of G De Michele including associated specialties, affiliations and a list of published articles.
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187
Citations
3607
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Recent Articles
1.
Lieto M, Riso V, Galatolo D, Rossi S, Barghigiani M, Cocozza S, et al.
Eur J Neurol
. 2019 Oct;
27(3):498-505.
PMID: 31571321
Background And Purpose: Heterozygous mutations in the STUB1 gene have recently been associated with an autosomal dominant form of spinocerebellar ataxia (SCA) associated with cerebellar cognitive-affective syndrome (CCAS), named SCA48....
2.
Mancini C, Giorgio E, Rubegni A, Pradotto L, Bagnoli S, Rubino E, et al.
Eur J Neurol
. 2018 Aug;
26(1):80-86.
PMID: 30098094
Background And Purpose: Hereditary ataxias are heterogeneous groups of neurodegenerative disorders, characterized by cerebellar syndromes associated with dysarthria, oculomotor and corticospinal signs, neuropathy and cognitive impairment. Recent reports have suggested...
3.
De Rosa A, Pellegrino T, Pappata S, Lieto M, Bonifati V, Palma V, et al.
Parkinsonism Relat Disord
. 2016 Jan;
23:102-5.
PMID: 26725142
Introduction: PARK20 is a rare autosomal recessive parkinsonism related to the SYNJ1 gene and characterized by early-onset of disease and atypical signs such as supranuclear vertical gaze palsy, dementia, dystonia,...
4.
Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay
Criscuolo C, Procaccini C, Meschini M, Cianflone A, Carbone R, Doccini S, et al.
J Neurol
. 2015 Nov;
262(12):2755-63.
PMID: 26530509
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disease due to mutations in SACS, which encodes sacsin, a protein localized on the mitochondrial surface and possibly involved in...
5.
Criscuolo C, Carbone R, Lieto M, Peluso S, Guacci A, Filla A, et al.
Acta Neurol Scand
. 2015 Sep;
133(6):410-4.
PMID: 26370385
Background: Autosomal recessive (AR) spastic paraplegia type 5 (SPG5) is due to mutations in the CYP7B1 gene, encoding for the cytochrome P450-7B1, responsible for oxysterols 7α-hydroxylation. Oxysterol/cholestenoic acids pool plays...
6.
Antenora A, Filla A, Santorelli F, Peluso S, Sacca F, De Michele G
Curr Mol Med
. 2014 Oct;
14(8):959-970.
PMID: 25323876
Metabolic ataxias are rare. They usually start in the childhood and often have autosomal recessive inheritance. They may also present in adulthood. The diagnosis is important since some patients may...
7.
Santangelo G, Vitale C, Trojano L, Picillo M, Moccia M, Pisano G, et al.
Eur J Neurol
. 2014 May;
22(2):253-60.
PMID: 24848193
Background And Purpose: Apathy may be either a symptom of major depression or a behavioral disturbance occurring in concomitance with depression or alone in Parkinson's disease (PD). The aim of...
8.
Pellecchia M, Santangelo G, Picillo M, Pivonello R, Longo K, Pivonello C, et al.
Eur J Neurol
. 2013 Apr;
21(5):802-7.
PMID: 23551560
Background And Purpose: Cognitive impairment is common in Parkinson's disease (PD), even in the early stages. We aimed to assess the relationship between insulin-like growth factor-1 (IGF-1) and cognitive functions...
9.
Pappata S, Santangelo G, Aarsland D, Vicidomini C, Longo K, Bronnick K, et al.
Neurology
. 2011 Sep;
77(14):1357-62.
PMID: 21940621
Objective: To characterize brain metabolic changes associated with mild cognitive impairment (MCI) in drug-naive patients with Parkinson disease (PD) using (18)F-fluorodeoxyglucose (FDG) and PET (FDG-PET). Methods: This cross-sectional study included...
10.
De Rosa A, Rinaldi C, Tucci T, Pappata S, Rossi F, Brescia Morra V, et al.
Parkinsonism Relat Disord
. 2011 Jul;
17(10):771-3.
PMID: 21733736
No abstract available.