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Giuseppe Plazzi
Giuseppe Plazzi
Alma Mater Studiorum, Bologna, Italy
Verified email at unibo.it
Title
Cited by
Cited by
Year
Validation of the International Restless Legs Syndrome Study Group rating scale for restless legs syndrome.
AS Walters, C LeBrocq, A Dhar, W Hening, R Rosen, RP Allen, ...
Sleep medicine 4 (2), 121, 2003
18092003
National Sleep Foundation's sleep quality recommendations: first report
M Ohayon, EM Wickwire, M Hirshkowitz, SM Albert, A Avidan, FJ Daly, ...
Sleep health 3 (1), 6-19, 2017
12922017
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
7612019
Nocturnal frontal lobe epilepsy: a clinical and polygraphic overview of 100 consecutive cases
F Provini, G Plazzi, P Tinuper, S Vandi, E Lugaresi, P Montagna
Brain 122 (6), 1017-1031, 1999
6441999
Narcolepsy is strongly associated with the T-cell receptor alpha locus
J Hallmayer, J Faraco, L Lin, S Hesselson, J Winkelmann, M Kawashima, ...
Nature genetics 41 (6), 708-711, 2009
5522009
The official World Association of Sleep Medicine (WASM) standards for recording and scoring periodic leg movements in sleep (PLMS) and wakefulness (PLMW) developed in …
M Zucconi, R Ferri, R Allen, PC Baier, O Bruni, S Chokroverty, ...
Sleep medicine 7 (2), 175-184, 2006
5112006
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
5041997
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
Elevated anti-streptococcal antibodies in patients with recent narcolepsy onset
A Aran, L Lin, S Nevsimalova, G Plazzi, SC Hong, K Weiner, J Zeitzer, ...
Sleep 32 (8), 979-983, 2009
4272009
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy
SE Heron, KR Smith, M Bahlo, L Nobili, E Kahana, L Licchetta, KL Oliver, ...
Nature genetics 44 (11), 1188-1190, 2012
4142012
Italian version of the Epworth sleepiness scale: external validity
L Vignatelli, G Plazzi, A Barbato, L Ferini-Strambi, R Manni, F Pompei, ...
Neurological Sciences 23, 295-300, 2003
3942003
REM sleep behaviour disorder
Y Dauvilliers, CH Schenck, RB Postuma, A Iranzo, PH Luppi, G Plazzi, ...
Nature reviews Disease primers 4 (1), 19, 2018
3892018
Narcolepsy as an autoimmune disease: the role of H1N1 infection and vaccination
M Partinen, BR Kornum, G Plazzi, P Jennum, I Julkunen, O Vaarala
The Lancet Neurology 13 (6), 600-613, 2014
3182014
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24
HA Phillips, IE Scheffer, KM Crossland, KP Bhatia, DR Fish, CD Marsden, ...
The American Journal of Human Genetics 63 (4), 1108-1116, 1998
3061998
The incidence of narcolepsy in Europe: before, during, and after the influenza A (H1N1) pdm09 pandemic and vaccination campaigns
L Wijnans, C Lecomte, C de Vries, D Weibel, C Sammon, A Hviid, ...
Vaccine 31 (8), 1246-1254, 2013
3032013
Neural network analysis of sleep stages enables efficient diagnosis of narcolepsy
JB Stephansen, AN Olesen, M Olsen, A Ambati, EB Leary, HE Moore, ...
Nature communications 9 (1), 5229, 2018
2862018
Insomnia, anxiety, and depression during the COVID-19 pandemic: an international collaborative study
CM Morin, B Bjorvatn, F Chung, B Holzinger, M Partinen, T Penzel, ...
Sleep medicine 87, 38-45, 2021
2812021
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
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
2691997
Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
J Winkelmann, L Lin, B Schormair, BR Kornum, J Faraco, G Plazzi, ...
Human molecular genetics 21 (10), 2205-2210, 2012
2672012
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