Maria Teresa Pellecchia
Maria Teresa Pellecchia
Professore di Neurologia, Università di Salerno
Verified email at
TitleCited byYear
The natural history of multiple system atrophy: a prospective European cohort study
GK Wenning, F Geser, F Krismer, K Seppi, S Duerr, S Boesch, ...
The lancet neurology 12 (3), 264-274, 2013
SNCA variants are associated with increased risk for multiple system atrophy
SW Scholz, H Houlden, C Schulte, M Sharma, A Li, D Berg, A Melchers, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians
D Ghezzi, C Marelli, A Achilli, S Goldwurm, G Pezzoli, P Barone, ...
European Journal of Human Genetics 13 (6), 748, 2005
Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry
M Köllensperger, F Geser, JP Ndayisaba, S Boesch, K Seppi, ...
Movement Disorders 25 (15), 2604-2612, 2010
Resting-state brain connectivity in patients with Parkinson's disease and freezing of gait
A Tessitore, M Amboni, F Esposito, A Russo, M Picillo, L Marcuccio, ...
Parkinsonism & related disorders 18 (6), 781-787, 2012
Red flags for multiple system atrophy
M Köllensperger, F Geser, K Seppi, M Stampfer‐Kountchev, M Sawires, ...
Movement disorders: official journal of the Movement Disorder Society 23 (8 …, 2008
Idiopathic cerebellar ataxia associated with celiac disease: lack of distinctive neurological features
MT Pellecchia, R Scala, A Filla, G De Michele, C Ciacci, P Barone
Journal of Neurology, Neurosurgery & Psychiatry 66 (1), 32-35, 1999
Progression of multiple system atrophy (MSA): a prospective natural history study by the European MSA Study Group (EMSA SG)
F Geser, GK Wenning, K Seppi, M Stampfer‐Kountchev, C Scherfler, ...
Movement disorders 21 (2), 179-186, 2006
The heterogeneity of early Parkinson’s disease: a cluster analysis on newly diagnosed untreated patients
R Erro, C Vitale, M Amboni, M Picillo, M Moccia, K Longo, G Santangelo, ...
PloS one 8 (8), e70244, 2013
The diverse phenotype and genotype of pantothenate kinase-associated neurodegeneration
MT Pellecchia, EM Valente, L Cif, S Salvi, A Albanese, V Scarano, ...
Neurology 64 (10), 1810-1812, 2005
Unawareness of dyskinesias in Parkinson's and Huntington's diseases
C Vitale, MT Pellecchia, D Grossi, N Fragassi, T Cuomo, L Di Maio, ...
Neurological Sciences 22 (1), 105-106, 2001
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group
C Kamm, DG Healy, NP Quinn, U Wüllner, JC Moller, L Schols, F Geser, ...
Brain 128 (8), 1855-1860, 2005
Non-motor symptoms in early Parkinson's disease: a 2-year follow-up study on previously untreated patients
R Erro, M Picillo, C Vitale, M Amboni, M Moccia, K Longo, A Cozzolino, ...
J Neurol Neurosurg Psychiatry 84 (1), 14-17, 2013
Health‐related quality of life in multiple system atrophy
A Schrag, F Geser, M Stampfer‐Kountchev, K Seppi, M Sawires, ...
Movement Disorders 21 (6), 809-815, 2006
Ropinirole as a treatment of restless legs syndrome in patients on chronic hemodialysis: an open randomized crossover trial versus levodopa sustained release
MT Pellecchia, C Vitale, M Sabatini, K Longo, M Amboni, V Bonavita, ...
Clinical neuropharmacology 27 (4), 178-181, 2004
Physical therapy in Parkinson’s disease: an open long-term rehabilitation trial
MT Pellecchia, A Grasso, LG Biancardi, M Squillante, V Bonavita, ...
Journal of neurology 251 (5), 595-598, 2004
Frontal dysfunction contributes to the genesis of hallucinations in non‐demented Parkinsonian patients
D Grossi, L Trojano, MT Pellecchia, M Amboni, NA Fragassi, P Barone
International Journal of Geriatric Psychiatry: A journal of the psychiatry …, 2005
Cerebellar ataxia associated with subclinical celiac disease responding to gluten-free diet
MT Pellecchia, R Scala, A Perretti, G De Michele, L Santoro, A Filla, ...
Neurology 53 (7), 1606-1606-a, 1999
The European multiple system atrophy-study group (EMSA-SG)
F Geser, K Seppi, M Stampfer-Kountchev, M Köllensperger, A Diem, ...
Journal of neural transmission 112 (12), 1677-1686, 2005
PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum
R Marongiu, A Ferraris, T Ialongo, S Michiorri, F Soleti, F Ferrari, AE Elia, ...
Human mutation 29 (4), 565-565, 2008
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