| 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 | 3379 | 2004 |
| 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 | 2421 | 2009 |
| 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 | 1877 | 2009 |
| 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: Basic and Clinical 161 (1), 46-48, 2011 | 1611 | 2011 |
| 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 | 933 | 1996 |
| 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 | 796 | 1992 |
| 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 | 731 | 1986 |
| 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 | 730 | 1992 |
| Sympathetic skin response R Vetrugno, R Liguori, P Cortelli, P Montagna Clinical autonomic research 13 (4), 256-270, 2003 | 490 | 2003 |
| 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 | 459 | 1997 |
| 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 | 400 | 2001 |
| Familial and sporadic fatal insomnia P Montagna, P Gambetti, P Cortelli, E Lugaresi The Lancet Neurology 2 (3), 167-176, 2003 | 362 | 2003 |
| 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 | 359 | 1994 |
| 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 | 347 | 2006 |
| 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 (5), 361-378, 2012 | 282 | 2012 |
| 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 | 241 | 1997 |
| 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 | 240 | 1992 |
| 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 | 238 | 2019 |
| 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 | 238 | 2005 |
| 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 | 238 | 1992 |