Maria Teresa Pellecchia
Overview
Explore the profile of Maria Teresa Pellecchia including associated specialties, affiliations and a list of published articles.
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Articles
171
Citations
3411
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Recent Articles
1.
Satolli S, Rossi S, Vegezzi E, Pellerin D, Manca M, Barghigiani M, et al.
J Neurol
. 2024 Nov;
271(12):7650-7651.
PMID: 39499281
No abstract available.
2.
Gandolfi M, Sandri A, Mariotto S, Tamburin S, Paolicelli A, Fiorio M, et al.
PLoS One
. 2024 Sep;
19(9):e0309408.
PMID: 39325803
Background And Aims: Functional motor disorders (FMD) present a prevalent, yet misunderstood spectrum of neurological conditions characterized by abnormal movements (i.e., functional limb weakness, tremor, dystonia, gait impairments), leading to...
3.
Abati E, Gagliardi D, Manini A, Del Bo R, Ronchi D, Meneri M, et al.
Brain Commun
. 2024 Sep;
6(5):fcae312.
PMID: 39315308
The gene encodes mitofusin 2, a key protein for mitochondrial fusion, transport, maintenance and cell communication. mutations are primarily linked to Charcot-Marie-Tooth disease type 2A. However, a few cases of...
4.
Tepedino M, Diana F, Abate F, Avallone A, Caterino M, Erro R, et al.
J Neurol
. 2024 Sep;
271(10):6866-6875.
PMID: 39222284
White matter hyperintensities (WMH) are considered magnetic brain imaging (MRI) biomarkers of cerebral small vessel disease but their clinical role in neurodegenerative-related disorders is poorly understood. This study describes the...
5.
Satolli S, Rossi S, Vegezzi E, Pellerin D, Manca M, Barghigiani M, et al.
J Neurol
. 2024 Jun;
271(8):5478-5488.
PMID: 38886208
Background: Autosomal-dominant spinocerebellar ataxia (ADCA) due to intronic GAA repeat expansion in FGF14 (SCA27B) is a recent, relatively common form of late-onset ataxia. Objective: Here, we aimed to: (1) investigate...
6.
Sorrentino C, Dati G, Cuoco S, Barone P, Pellecchia M
Mov Disord Clin Pract
. 2024 Jun;
11(8):1030-1034.
PMID: 38881158
Background: Heterozygous mutations in GBA1 gene are known as most common genetic risk factor for Parkinson's disease (PD). However, role of GBA1 mutations in non-α-synuclein disorders is unclear. Cases: Case...
7.
Chia R, Ray A, Shah Z, Ding J, Ruffo P, Fujita M, et al.
Neuron
. 2024 May;
112(13):2142-2156.e5.
PMID: 38701790
Multiple system atrophy (MSA) is an adult-onset, sporadic synucleinopathy characterized by parkinsonism, cerebellar ataxia, and dysautonomia. The genetic architecture of MSA is poorly understood, and treatments are limited to supportive...
8.
Tepedino M, Avallone A, Abate F, Serio M, Caterino M, Erro R, et al.
Neurol Sci
. 2024 Apr;
45(9):4335-4340.
PMID: 38639893
Introduction: Alterations in metabolic status, body composition, and food intake are present in all neurodegenerative diseases. Aim of this study was to detect the progression of these changes in Progressive...
9.
Cappiello A, Abate F, Adamo S, Tepedino M, Donisi L, Ricciardi C, et al.
Mov Disord
. 2024 Mar;
39(6):1043-1048.
PMID: 38468604
Background: Progressive supranuclear palsy (PSP) is a rare 4R-tauopathy. Transcranial direct current stimulation (tDCS) may improve specific symptoms. Objectives: This randomized, double-blinded, sham-controlled trial aimed at verifying the short-, mid-,...
10.
Cuoco S, Blundo C, Ricci M, Cappiello A, Bisogno R, Carotenuto I, et al.
J Neural Transm (Vienna)
. 2024 Jan;
131(2):173-180.
PMID: 38200268
Objectives: The Caregiver's Inventory Neuropsychological Diagnosis Dementia (CINDD) is an easy tool designed to quantify cognitive, behavioural and functional deficits of patients with cognitive impairment. Aim of the present study...