Pietro Cortelli
Pietro Cortelli
DIBINEM - University of Bologna; IRCCS-ISN
Verified email at unibo.it
TitleCited byYear
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
28092004
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
TJ Kwiatkowski, DA Bosco, AL Leclerc, E Tamrazian, CR Vanderburg, ...
Science 323 (5918), 1205-1208, 2009
19552009
Guidelines: 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 …
A Moya, R Sutton, F Ammirati, JJ Blanc, M Brignole, JB Dahm, JC Deharo, ...
European heart journal 30 (21), 2631, 2009
16972009
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, ...
Clinical Autonomic Research 21 (2), 69-72, 2011
10962011
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
8371996
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
7491992
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei
E Lugaresi, R Medori, P Montagna, A Baruzzi, P Cortelli, A Lugaresi, ...
New England Journal of Medicine 315 (16), 997-1003, 1986
6771986
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
6711992
Sympathetic skin response
R Vetrugno, R Liguori, P Cortelli, P Montagna
Clinical autonomic research 13 (4), 256-270, 2003
4102003
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
4081997
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
3622001
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
3281994
Familial and sporadic fatal insomnia
P Montagna, P Gambetti, P Cortelli, E Lugaresi
The Lancet Neurology 2 (3), 167-176, 2003
3062003
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
2942006
Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178
R Medori, P Montagna, HJ Tritschler, A LeBlanc, P Cortelli, P Tinuper, ...
Neurology 42 (3), 669-669, 1992
2271992
Fatal familial insomnia: clinical and pathologic study of five new cases
V Manetto, R Medori, P Cortelli, P Montagna, P Tinuper, A Baruzzi, ...
Neurology 42 (2), 312-312, 1992
2241992
Undiagnosed sleep-disordered breathing among male nondippers with essential hypertension
F Portaluppi, F Provini, P Cortelli, G Plazzi, N Bertozzi, R Manfredini, ...
Journal of hypertension 15 (11), 1227-1233, 1997
2231997
Abnormal brain and muscle energy metabolism shown by 31P magnetic resonance spectroscopy in patients affected by migraine with aura
B Barbiroli, P Montagna, P Cortelli, R Funicello, S Iotti, L Monari, ...
Neurology 42 (6), 1209-1209, 1992
2161992
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
2082005
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
1922005
The system can't perform the operation now. Try again later.
Articles 1–20