20062020

Research output per year

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Research Output

2020

Clinical Reasoning: Young woman with orbital pain and diplopia

Infante, R., Donadio, V., Nucera, B., Toni, F., Marliani, F., Liguori, R. & Licchetta, L., Feb 18 2020, In : Neurology. 94, 7, p. e752-e757

Research output: Contribution to journalArticle

FDG-PET assessment and metabolic patterns in Lafora disease

Muccioli, L., Farolfi, A., Pondrelli, F., d’Orsi, G., Michelucci, R., Freri, E., Canafoglia, L., Licchetta, L., Toni, F., Bonfiglioli, R., Civollani, S., Pettinato, C., Maietti, E., Marotta, G., Fanti, S., Tinuper, P. & Bisulli, F., 2020, In : European Journal of Nuclear Medicine and Molecular Imaging. 47, 6, p. 1576-1584

Research output: Contribution to journalArticle

Ictal vasodepressive syncope in temporal lobe epilepsy

Mastrangelo, V., Bisulli, F., Muccioli, L., Licchetta, L., Menghi, V., Alvisi, L., Barletta, G., Ribani, M. A., Cortelli, P. & Tinuper, P., Jan 2020, In : Clinical Neurophysiology. 131, 1, p. 155-157 3 p.

Research output: Contribution to journalLetter

Open Access

Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients

On behalf of the Collaborative Group of Italian League Against Epilepsy (LICE) Genetic Study Group on SHE, Jan 2020, In : Seizure. 74, p. 60-64 5 p.

Research output: Contribution to journalArticle

Therapy in Sleep-Related Hypermotor Epilepsy (SHE)

Asioli, G. M., Rossi, S., Bisulli, F., Licchetta, L., Tinuper, P. & Provini, F., Jan 1 2020, In : Current Treatment Options in Neurology. 22, 1, 1.

Research output: Contribution to journalReview article

2019

An Italian multicentre study of perampanel in progressive myoclonus epilepsies

Canafoglia, L., Barbella, G., Ferlazzo, E., Striano, P., Magaudda, A., d'Orsi, G., Martino, T., Avolio, C., Aguglia, U., Sueri, C., Giuliano, L., Sofia, V., Zibordi, F., Ragona, F., Freri, E., Costa, C., Nardi Cesarini, E., Fanella, M., Rossi Sebastiano, D., Riguzzi, P. & 10 others, Gambardella, A., Di Bonaventura, C., Michelucci, R., Granata, T., Bisulli, F., Licchetta, L., Tinuper, P., Beccaria, F., Visani, E. & Franceschetti, S., Oct 1 2019, In : Epilepsy Research. 156, 106191.

Research output: Contribution to journalArticle

Clinical features and pathophysiology of disorders of arousal in adults: A window into the sleeping brain

Baldini, T., Loddo, G., Sessagesimi, E., Mignani, F., Cirignotta, F., Mondini, S., Licchetta, L., Bisulli, F., Tinuper, P. & Provini, F., Jan 1 2019, In : Frontiers in Neurology. 10, MAY, 526.

Research output: Contribution to journalArticle

Open Access

Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies

the Collaborative Group of Italian League Against Epilepsy (LICE) Genetic Commission, Mar 1 2019, In : Annals of Clinical and Translational Neurology. 6, 3, p. 475-485 11 p.

Research output: Contribution to journalArticle

Open Access

FDG-PET assessment and metabolic patterns in Lafora disease

Muccioli, L., Farolfi, A., Pondrelli, F., d'Orsi, G., Michelucci, R., Freri, E., Canafoglia, L., Licchetta, L., Toni, F., Bonfiglioli, R., Civollani, S., Pettinato, C., Maietti, E., Marotta, G., Fanti, S., Tinuper, P. & Bisulli, F., Dec 19 2019, In : European Journal of Nuclear Medicine and Molecular Imaging.

Research output: Contribution to journalArticle

Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2

Corbett, M. A., Kroes, T., Veneziano, L., Bennett, M. F., Florian, R., Schneider, A. L., Coppola, A., Licchetta, L., Franceschetti, S., Suppa, A., Wenger, A., Mei, D., Pendziwiat, M., Kaya, S., Delledonne, M., Straussberg, R., Xumerle, L., Regan, B., Crompton, D., van Rootselaar, A. F. & 49 others, Correll, A., Catford, R., Bisulli, F., Chakraborty, S., Baldassari, S., Tinuper, P., Barton, K., Carswell, S., Smith, M., Berardelli, A., Carroll, R., Gardner, A., Friend, K. L., Blatt, I., Iacomino, M., Di Bonaventura, C., Striano, S., Buratti, J., Keren, B., Nava, C., Forlani, S., Rudolf, G., Hirsch, E., Leguern, E., Labauge, P., Balestrini, S., Sander, J. W., Afawi, Z., Helbig, I., Ishiura, H., Tsuji, S., Sisodiya, S. M., Casari, G., Sadleir, L. G., van Coller, R., Tijssen, M. A. J., Klein, K. M., van den Maagdenberg, A. M. J. M., Zara, F., Guerrini, R., Berkovic, S. F., Pippucci, T., Canafoglia, L., Bahlo, M., Striano, P., Scheffer, I. E., Brancati, F., Depienne, C. & Gecz, J., Dec 1 2019, In : Nature Communications. 10, 1, 4920.

Research output: Contribution to journalArticle

Open Access

Polysomnographic features differentiating disorder of arousals from sleep-related hypermotor epilepsy

Proserpio, P., Loddo, G., Zubler, F., Ferini-Strambi, L., Licchetta, L., Bisulli, F., Tinuper, P., Agostoni, E. C., Bassetti, C., Tassi, L., Menghi, V., Provini, F. & Nobili, L., Dec 24 2019, In : Sleep. 42, 12

Research output: Contribution to journalArticle

SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus

Bisulli, F., Licchetta, L., Baldassari, S., Muccioli, L., Marconi, C., Cantalupo, G., Myers, C., Menghi, V., Minardi, R., Caporali, L., Marini, C., Guerrini, R., Mefford, H. C., Tinuper, P. & Pippucci, T., Apr 2019, In : Epileptic Disorders. 21, 2, p. 185-191 7 p.

Research output: Contribution to journalArticle

Treatment with metformin in twelve patients with Lafora disease

Bisulli, F., Muccioli, L., D'Orsi, G., Canafoglia, L., Freri, E., Licchetta, L., Mostacci, B., Riguzzi, P., Pondrelli, F., Avolio, C., Martino, T., Michelucci, R. & Tinuper, P., Jun 21 2019, In : Orphanet Journal of Rare Diseases. 14, 1, 149.

Research output: Contribution to journalArticle

Open Access

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Epi25 Collaborative. Electronic address: s.berkovic@unimelb.edu.au, Aug 1 2019, In : American Journal of Human Genetics. 105, 2, p. 267-282 16 p.

Research output: Contribution to journalArticle

2018

Cortical myoclonic tremor induced by fixation-off sensitivity: An unusual cause of insomnia

Licchetta, L., Bisulli, F., Ferri, L., Cantalupo, G., Alvisi, L., Vignatelli, L., Loddo, G., Provini, F. & Tinuper, P., Dec 4 2018, In : Neurology. 91, 23, p. 1061-1063 3 p.

Research output: Contribution to journalArticle

Effect of valproic acid on perampanel pharmacokinetics in patients with epilepsy

the Perampanel Study Group, Jul 1 2018, In : Epilepsia. 59, 7, p. e103-e108

Research output: Contribution to journalArticle

Epilepsy with auditory features: Long-term outcome and predictors of terminal remission

Bisulli, F., Menghi, V., Vignatelli, L., Licchetta, L., Zenesini, C., Stipa, C., Morigi, F., Gizzi, M., Avoni, P., Provini, F., Mostacci, B., d'Orsi, G., Pippucci, T., Muccioli, L. & Tinuper, P., Apr 1 2018, In : Epilepsia. 59, 4, p. 834-843 10 p.

Research output: Contribution to journalArticle

Estrogen-related seizure exacerbation following hormone therapy for assisted reproduction in women with epilepsy

Mostacci, B., Esposto, R., Lello, S., Bisulli, F., Licchetta, L. & Tinuper, P., Oct 1 2018, In : Seizure. 61, p. 200-202 3 p.

Research output: Contribution to journalArticle

Juvenile absence epilepsy relapsing as recurrent absence status, mimicking transient global amnesia, in an elderly patient

Muccioli, L., Licchetta, L., Stipa, C., Tinuper, P. & Bisulli, F., Dec 1 2018, In : Epileptic Disorders. 20, 6, p. 557-561 5 p.

Research output: Contribution to journalArticle

Nocturnal motor behaviors with unexpected EEG and brain MRI findings

Baldini, T., Loddo, G., Mignani, F., Licchetta, L., Bisulli, F., Tinuper, P. & Provini, F., Dec 1 2018, In : Sleep Medicine. 52, p. 116-117 2 p.

Research output: Contribution to journalLetter

Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations

Di Vito, L., Licchetta, L., Pippucci, T., Baldassari, S., Stipa, C., Mostacci, B., Alvisi, L., Tinuper, P. & Bisulli, F., Feb 1 2018, In : Epilepsy and Behavior. 79, p. 169-173 5 p.

Research output: Contribution to journalArticle

Profile of neuropsychological impairment in Sleep-related Hypermotor Epilepsy

Licchetta, L., Poda, R., Vignatelli, L., Pippucci, T., Zenesini, C., Menghi, V., Mostacci, B., Baldassari, S., Provini, F., Tinuper, P. & Bisulli, F., Aug 1 2018, In : Sleep Medicine. 48, p. 8-15 8 p.

Research output: Contribution to journalArticle

Specific motor patterns of arousal disorders in adults: A video-polysomnographic analysis of 184 episodes

Loddo, G., Sessagesimi, E., Mignani, F., Cirignotta, F., Mondini, S., Licchetta, L., Bisulli, F., Tinuper, P. & Provini, F., 2018, In : Sleep Medicine. 41, p. 102-9

Research output: Contribution to journalArticle

The landscape of epilepsy-related GATOR1 variants

Baldassari, S., Picard, F., Verbeek, N. E., van Kempen, M., Brilstra, E. H., Lesca, G., Conti, V., Guerrini, R., Bisulli, F., Licchetta, L., Pippucci, T., Tinuper, P., Hirsch, E., de Saint Martin, A., Chelly, J., Rudolf, G., Chipaux, M., Ferrand-Sorbets, S., Dorfmüller, G., Sisodiya, S. & 69 others, Balestrini, S., Schoeler, N., Hernandez-Hernandez, L., Krithika, S., Oegema, R., Hagebeuk, E., Gunning, B., Deckers, C., Berghuis, B., Wegner, I., Niks, E., Jansen, F. E., Braun, K., de Jong, D., Rubboli, G., Talvik, I., Sander, V., Uldall, P., Jacquemont, M. L., Nava, C., Leguern, E., Julia, S., Gambardella, A., d’Orsi, G., Crichiutti, G., Faivre, L., Darmency, V., Benova, B., Krsek, P., Biraben, A., Lebre, A. S., Jennesson, M., Sattar, S., Marchal, C., Nordli, D. R., Lindstrom, K., Striano, P., Lomax, L. B., Kiss, C., Bartolomei, F., Lepine, A. F., Schoonjans, A. S., Stouffs, K., Jansen, A., Panagiotakaki, E., Ricard-Mousnier, B., Thevenon, J., de Bellescize, J., Catenoix, H., Dorn, T., Zenker, M., Müller-Schlüter, K., Brandt, C., Krey, I., Polster, T., Wolff, M., Balci, M., Rostasy, K., Achaz, G., Zacher, P., Becher, T., Cloppenborg, T., Yuskaitis, C. J., Weckhuysen, S., Poduri, A., Lemke, J. R., Møller, R. S., Baulac, S. & Baulac, S., 2018, In : Genetics in Medicine.

Research output: Contribution to journalArticle

2017

A stereo EEG study in a patient with sleep-related hypermotor epilepsy due to DEPDC5 mutation

Ferri, L., Bisulli, F., Mai, R., Licchetta, L., Leta, C., Nobili, L., Mostacci, B., Pippucci, T. & Tinuper, P., Dec 1 2017, In : Seizure. 53, p. 51-54 4 p.

Research output: Contribution to journalArticle

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties

Oliver, K. L., Franceschetti, S., Milligan, C. J., Muona, M., Mandelstam, S. A., Canafoglia, L., Boguszewska-Chachulska, A. M., Korczyn, A. D., Bisulli, F., Di Bonaventura, C., Ragona, F., Michelucci, R., Ben-Zeev, B., Straussberg, R., Panzica, F., Massano, J., Friedman, D., Crespel, A., Engelsen, B. A., Andermann, F. & 20 others, Andermann, E., Spodar, K., Lasek-Bal, A., Riguzzi, P., Pasini, E., Tinuper, P., Licchetta, L., Gardella, E., Lindenau, M., Wulf, A., Møller, R. S., Benninger, F., Afawi, Z., Rubboli, G., Reid, C. A., Maljevic, S., Lerche, H., Lehesjoki, A. E., Petrou, S. & Berkovic, S. F., May 1 2017, In : Annals of Neurology. 81, 5, p. 677-689 13 p.

Research output: Contribution to journalArticle

Prevalence of sleep-related hypermotor epilepsy-formerly named nocturnal frontal lobe epilepsy-in the adult population of the emilia-romagna region, Italy

Vignatelli, L., Bisulli, F., Giovannini, G., Licchetta, L., Naldi, I., Mostacci, B., Rubboli, G., Provini, F., Tinuper, P. & Meletti, S., Feb 1 2017, In : Sleep. 40, 2, zsw041.

Research output: Contribution to journalLetter

Proton MR spectroscopy in patients with sleep-related hypermotor epilepsy (SHE): Evidence of altered cingulate cortex metabolism

Naldi, I., Bisulli, F., Testa, C., Rizzo, G., Ferri, L., Gramegna, L. L., Licchetta, L., Lodi, R., Tonon, C. & Tinuper, P., 2017, In : Sleep. 40, 9, zsx115.

Research output: Contribution to journalArticle

Sleep-related hypermotor epilepsy: Long-term outcome in a large cohort

Licchetta, L., Bisulli, F., Vignatelli, L., Zenesini, C., Di Vito, L., Mostacci, B., Rinaldi, C., Trippi, I., Naldi, I., Plazzi, G., Provini, F. & Tinuper, P., Jan 3 2017, In : Neurology. 88, 1, p. 70-77 8 p.

Research output: Contribution to journalArticle

2016

Behçet disease presenting with movement disorders and antibasal ganglia antibodies

Rizzo, G., Licchetta, L., Scaglione, C., Buttiglione, M., Capellari, S., Martinelli, P. & Martino, D., Mar 1 2016, In : Autoimmunity Reviews. 15, 3, p. 287-288 2 p.

Research output: Contribution to journalArticle

Definition and diagnostic criteria of sleep-related hypermotor epilepsy

Tinuper, P., Bisulli, F., Cross, J. H., Hesdorffer, D. C., Kahane, P., Nobili, L., Provini, F., Scheffer, I. E., Tassi, L., Vignatelli, L., Bassetti, C. L., Cirignotta, F., Derry, C., Gambardella, A., Guerrini, R., Halasz, P., Licchetta, L., Mahowald, M., Manni, R., Marini, C. & 10 others, Mostacci, B., Naldi, I., Parrino, L., Picard, F., Pugliatti, M., Ryvlin, P., Vigevano, F., Zucconi, M., Berkovic, S. F. & Ottman, R., May 10 2016, In : Neurology. 86, 19, p. 1834-1842 9 p.

Research output: Contribution to journalReview article

Definition and diagnostic criteria of sleep-related hypermotor epilepsy

Tinuper, P., Bisulli, F., Cross, J. H., Hesdorffer, D., Kahane, P., Nobili, L., Provini, F., Scheffer, I. E., Tassi, L., Vignatelli, L., Bassetti, C., Cirignotta, F., Derry, C., Gambardella, A., Guerrini, R., Halasz, P., Licchetta, L., Mahowald, M., Manni, R., Marini, C. & 10 others, Mostacci, B., Naldi, I., Parrino, L., Picard, F., Pugliatti, M., Ryvlin, P., Vigevano, F., Zucconi, M., Berkovic, S. & Ottman, R., May 10 2016, In : Neurology. 86, 19, p. 1834-1842 9 p.

Research output: Contribution to journalReview article

Definition and diagnostic criteria of sleep-related hypermotor epilepsy

Tinuper, P., Bisulli, F., Cross, J. H., Hesdorffer, D. C., Kahane, P., Nobili, L., Provini, F., Scheffer, I. E., Tassi, L., Vignatelli, L., Bassetti, C. L., Cirignotta, F., Derry, C., Gambardella, A., Guerrini, R., Halasz, P., Licchetta, L., Mahowald, M., Manni, R., Marini, C. & 10 others, Mostacci, B., Naldi, I., Parrino, L., Picard, F., Pugliatti, M., Ryvlin, P., Vigevano, F., Zucconi, M., Berkovic, S. F. & Ottman, R., May 10 2016, In : Neurology. 86, 19, p. 1834-1842 9 p.

Research output: Contribution to journalReview article

Definition and diagnostic criteria of sleep-related hypermotor epilepsy

Tinuper, P., Bisulli, F., Cross, J. H., Hesdorffer, D. C., Kahane, P., Nobili, L., Provini, F., Scheffer, I. E., Tassi, L., Vignatelli, L., Bassetti, C. L., Cirignotta, F., Derry, C., Gambardella, A., Guerrini, R., Halasz, P., Licchetta, L., Mahowald, M., Manni, R., Marini, C. & 10 others, Mostacci, B., Naldi, I., Parrino, L., Picard, F., Pugliatti, M., Ryvlin, P., Vigevano, F., Zucconi, M., Berkovic, S. F. & Ottman, R., May 10 2016, In : Neurology. 86, 19, p. 1834-1842 9 p.

Research output: Contribution to journalReview article

DEPDC5 mutations in epilepsy with auditory features

Bisulli, F., Licchetta, L., Baldassari, S., Pippucci, T. & Tinuper, P., Feb 1 2016, In : Epilepsia. 57, 2, p. 335 1 p.

Research output: Contribution to journalArticle

Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)

ANCL Gene Discovery Consortium, Bisulli, F., Licchetta, L. & Tinuper, P., Aug 9 2016, In : Neurology. 87, 6, p. 579-584 6 p.

Research output: Contribution to journalArticle

Epilepsy in ring chromosome 20 syndrome

Vignoli, A., Bisulli, F., Darra, F., Mastrangelo, M., Barba, C., Giordano, L., Turner, K., Zambrelli, E., Chiesa, V., Bova, S., Fiocchi, I., Peron, A., Naldi, I., Milito, G., Licchetta, L., Tinuper, P., Guerrini, R., Dalla Bernardina, B. & Canevini, M. P., Dec 1 2016, In : Epilepsy Research. 128, p. 83-93 11 p.

Research output: Contribution to journalArticle

GATOR1 complex: The common genetic actor in focal epilepsies

Baldassari, S., Licchetta, L., Tinuper, P., Bisulli, F. & Pippucci, T., 2016, In : Journal of Medical Genetics. 53, p. 503-10

Research output: Contribution to journalArticle

Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2

Henden, L., Freytag, S., Afawi, Z., Baldassari, S., Berkovic, S. F., Bisulli, F., Canafoglia, L., Casari, G., Crompton, D. E., Depienne, C., Gecz, J., Guerrini, R., Helbig, I., Hirsch, E., Keren, B., Klein, K. M., Labauge, P., LeGuern, E., Licchetta, L., Mei, D. & 9 others, Nava, C., Pippucci, T., Rudolf, G., Scheffer, I. E., Striano, P., Tinuper, P., Zara, F., Corbett, M. & Bahlo, M., 2016, In : Human Genetics. 135, 10, p. 1117-25

Research output: Contribution to journalArticle

Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2

Henden, L., Freytag, S., Afawi, Z., Baldassari, S., Berkovic, S. F., Bisulli, F., Canafoglia, L., Casari, G. N., Crompton, D. E., Depienne, C., Gecz, J., Guerrini, R., Helbig, I., Hirsch, E., Keren, B., Klein, K. M., Labauge, P., Leguern, E., Licchetta, L., Mei, D. & 9 others, Nava, C., Pippucci, T., Rudolf, G., Scheffer, I. E., Striano, P., Tinuper, P., Zara, F., Corbett, M. A. & Bahlo, M., Jul 1 2016, (Accepted/In press) In : Human Genetics. p. 1-9 9 p.

Research output: Contribution to journalArticle

Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2

Henden, L., Freytag, S., Afawi, Z., Baldassari, S., Berkovic, S. F., Bisulli, F., Canafoglia, L., Casari, G. N., Crompton, D. E., Depienne, C., Gecz, J., Guerrini, R., Helbig, I., Hirsch, E., Keren, B., Klein, K. M., Labauge, P., Leguern, E., Licchetta, L., Mei, D. & 9 others, Nava, C., Pippucci, T., Rudolf, G., Scheffer, I. E., Striano, P., Tinuper, P., Zara, F., Corbett, M. A. & Bahlo, M., 2016, In : Human Genetics. p. 1-9 9 p.

Research output: Contribution to journalArticle

Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2

Henden, L., Freytag, S., Afawi, Z., Baldassari, S., Berkovic, S. F., Bisulli, F., Canafoglia, L., Casari, G., Crompton, D. E., Depienne, C., Gecz, J., Guerrini, R., Helbig, I., Hirsch, E., Keren, B., Klein, K. M., Labauge, P., LeGuern, E., Licchetta, L., Mei, D. & 9 others, Nava, C., Pippucci, T., Rudolf, G., Scheffer, I. E., Striano, P., Tinuper, P., Zara, F., Corbett, M. & Bahlo, M., Oct 1 2016, In : Human Genetics. 135, 10, p. 1117 - 1125 9 p.

Research output: Contribution to journalArticle

Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy

Ricos, M. G., Hodgson, B. L., Pippucci, T., Saidin, A., Ong, Y. S., Heron, S. E., Licchetta, L., Bisulli, F., Bayly, M. A., Hughes, J., Baldassari, S., Palombo, F., Santucci, M., Meletti, S., Berkovic, S. F., Rubboli, G., Thomas, P. Q., Scheffer, I. E., Tinuper, P., Geoghegan, J. & 2 others, Schreiber, A. W. & Dibbens, L. M., Jan 1 2016, In : Annals of Neurology. 79, 1, p. 120-131 12 p.

Research output: Contribution to journalArticle

Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy

Coppola, A., Caccavale, C., Santulli, L., Balestrini, S., Cagnetti, C., Licchetta, L., Esposito, M., Bisulli, F., Tinuper, P., Provinciali, L., Minetti, C., Zara, F., Striano, P. & Striano, S., Mar 1 2016, In : Epilepsy and Behavior. 56, p. 38-43 6 p.

Research output: Contribution to journalArticle

2015

A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy

Licchetta, L., Bisulli, F., Fietz, M., Valentino, M. L., Morbin, M., Mostacci, B., Oliver, K. L., Berkovic, S. F. & Tinuper, P., Oct 1 2015, In : European Journal of Medical Genetics. 58, 10, p. 540-544 5 p.

Research output: Contribution to journalArticle

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

Muona, M., Berkovic, S. F., Dibbens, L. M., Oliver, K. L., Maljevic, S., Bayly, M. A., Joensuu, T., Canafoglia, L., Franceschetti, S., Michelucci, R., Markkinen, S., Heron, S. E., Hildebrand, M. S., Andermann, E., Andermann, F., Gambardella, A., Tinuper, P., Licchetta, L., Scheffer, I. E., Criscuolo, C. & 31 others, Filla, A., Ferlazzo, E., Ahmad, J., Ahmad, A., Baykan, B., Said, E., Topcu, M., Riguzzi, P., King, M. D., Ozkara, C., Andrade, D. M., Engelsen, B. A., Crespel, A., Lindenau, M., Lohmann, E., Saletti, V., Massano, J., Privitera, M., Espay, A. J., Kauffmann, B., Duchowny, M., Møller, R. S., Straussberg, R., Afawi, Z., Ben-Zeev, B., Samocha, K. E., Daly, M. J., Petrou, S., Lerche, H., Palotie, A. & Lehesjoki, A. E., Jan 1 2015, In : Nature Genetics. 47, 1, p. 39-46 8 p.

Research output: Contribution to journalArticle

Incidence of sudden unexpected death in nocturnal frontal lobe epilepsy: A cohort study

Mostacci, B., Bisulli, F., Vignatelli, L., Licchetta, L., Di Vito, L., Rinaldi, C., Trippi, I., Ferri, L., Plazzi, G., Provini, F. & Tinuper, P., Feb 1 2015, In : Sleep Medicine. 16, 2, p. 232-236 5 p.

Research output: Contribution to journalArticle