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Pietro Cortelli
Pietro Cortelli
DIBINEM - University of Bologna; IRCCS-ISN
在 unibo.it 的电子邮件经过验证
标题
引用次数
引用次数
年份
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
EM Valente, PM Abou-Sleiman, V Caputo, MMK Muqit, K Harvey, ...
Science 304 (5674), 1158-1160, 2004
41772004
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
TJ Kwiatkowski Jr, DA Bosco, AL Leclerc, E Tamrazian, CR Vanderburg, ...
Science 323 (5918), 1205-1208, 2009
30732009
Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome
R Freeman, W Wieling, FB Axelrod, DG Benditt, E Benarroch, I Biaggioni, ...
Autonomic Neuroscience 161 (1-2), 46-48, 2011
22992011
Guidelines for the diagnosis and management of syncope (version 2009): the Task Force for the Diagnosis and Management of Syncope of the European Society of Cardiology (ESC)
A Moya, R Sutton
European heart journal 30 (21), 2631-2671, 2009
21062009
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity
GC Telling, P Parchi, SJ DeArmond, P Cortelli, P Montagna, R Gabizon, ...
Science 274 (5295), 2079-2082, 1996
10591996
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism
LG Goldfarb, RB Petersen, M Tabaton, P Brown, AC LeBlanc, P Montagna, ...
Science 258 (5083), 806-808, 1992
8801992
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei.
E Lugaresi, R Medori, P Montagna, A Baruzzi, P Cortelli, A Lugaresi, ...
The New England journal of medicine, 1986
8491986
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
R Medori, HJ Tritschler, A LeBlanc, F Villare, V Manetto, HY Chen, R Xue, ...
New England Journal of Medicine 326 (7), 444-449, 1992
8461992
Risk and predictors of dementia and parkinsonism in idiopathic REM sleep behaviour disorder: a multicentre study
RB Postuma, A Iranzo, M Hu, B Högl, BF Boeve, R Manni, WH Oertel, ...
Brain 142 (3), 744-759, 2019
7582019
Sympathetic skin response: basic mechanisms and clinical applications
R Vetrugno, R Liguori, P Cortelli, P Montagna
Clinical autonomic research 13, 256-270, 2003
5992003
REM sleep behavior disorders in multiple system atrophy
G Plazzi, R Corsini, F Provini, G Pierangeli, P Martinelli, P Montagna, ...
Neurology 48 (4), 1094-1096, 1997
5031997
Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels
R Liguori, A Vincent, L Clover, P Avoni, G Plazzi, P Cortelli, A Baruzzi, ...
Brain 124 (12), 2417-2426, 2001
4522001
EFNS guidelines on the diagnosis and management of orthostatic hypotension
H Lahrmann, P Cortelli, M Hilz, CJ Mathias, W Struhal, M Tassinari
European journal of neurology 13 (9), 930-936, 2006
4322006
Familial and sporadic fatal insomnia
P Montagna, P Gambetti, P Cortelli, E Lugaresi
The Lancet Neurology 2 (3), 167-176, 2003
4162003
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
L Monari, SG Chen, P Brown, P Parchi, RB Petersen, J Mikol, F Gray, ...
Proceedings of the National Academy of Sciences 91 (7), 2839-2842, 1994
4011994
Cost of healthcare for patients with migraine in five European countries: results from the International Burden of Migraine Study (IBMS)
LM Bloudek, M Stokes, DC Buse, TK Wilcox, RB Lipton, PJ Goadsby, ...
The journal of headache and pain 13, 361-378, 2012
3722012
The movement disorder society criteria for the diagnosis of multiple system atrophy
GK Wenning, I Stankovic, L Vignatelli, A Fanciulli, G Calandra‐Buonaura, ...
Movement Disorders 37 (6), 1131-1148, 2022
3092022
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
DJH Moss, AF Pardiñas, D Langbehn, K Lo, BR Leavitt, R Roos, A Durr, ...
The Lancet Neurology 16 (9), 701-711, 2017
3062017
Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy
P Barboni, G Savini, ML Valentino, P Montagna, P Cortelli, AM De Negri, ...
Ophthalmology 112 (1), 120-126, 2005
2812005
Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies
M Rossi, N Candelise, S Baiardi, S Capellari, G Giannini, CD Orrù, ...
Acta neuropathologica 140, 49-62, 2020
2712020
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