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Research Output 2006 2019

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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

Progressive Myoclonic Epilepsy
Myoclonus
Multicenter Studies
Seizures
Psychiatry

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
Arousal
Brain
Polysomnography
Video Recording
Sleep

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
Partial Epilepsy
Sirolimus
Genes
Gene Components
Exome

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

Lafora Disease
Positron-Emission Tomography
Frontal Lobe
Temporal Lobe
Thalamus

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., Jan 1 2019, (Accepted/In press) In : European Journal of Nuclear Medicine and Molecular Imaging.

Research output: Contribution to journalArticle

Lafora Disease
Positron-Emission Tomography
Frontal Lobe
Temporal Lobe
Thalamus

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
epilepsy
Myoclonic Epilepsy
Chromosomes, Human, Pair 2
chromosomes
Chromosomes

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

Sleep Arousal Disorders
Epilepsy
Arousal
Sleep
Sensitivity and Specificity

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

Partial Epilepsy
Epilepsy
Mutation
Febrile Seizures
Nuclear Family
Epilepsy
Sleep
Seizures
Cohort Studies
Wakefulness

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
Lafora Disease
Metformin
Therapeutics
Progressive Myoclonic Epilepsy
Orphaned Children
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

Sleep Initiation and Maintenance Disorders
Tremor
Sleep
Electroencephalography
Seizures

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

Valproic Acid
Epilepsy
Pharmacokinetics
Enzymes
zonisamide

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

Epilepsy
Electroencephalography
Hallucinations
Scalp
Age of Onset

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

Reproduction
Epilepsy
Estrogens
Seizures
Hormones

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

Transient Global Amnesia
Absence Epilepsy
Status Epilepticus
Electroencephalography
Seizures

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

Phenotype
Mutation
Genes
Epilepsy
Glucose Transporter Type 1

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

Epilepsy
Sleep
Intellectual Disability
Neurologic Examination
Nonparametric Statistics

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

Arousal
Somnambulism
Video Recording
Head
Head Movements

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

Epilepsy
Seizures
Partial Epilepsy
Sudden Death
Genes
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

Electroencephalography
Epilepsy
Sleep
Mutation
Malformations of Cortical Development

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

Myoclonic Epilepsy
Myoclonus
Fever
Mutation
Temperature

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

Gyrus Cinguli
Protons
Epilepsy
Sleep
Magnetic Resonance Spectroscopy

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

Epilepsy
Sleep
Seizures
Wakefulness
Brain Diseases
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

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

Epilepsy
Seizures
Age of Onset
Status Epilepticus
Ring Chromosome 20 Syndrome

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

Partial Epilepsy
Sirolimus
Epilepsy
Malformations of Cortical Development
Gene Components

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

Myoclonic Epilepsy
Genes
Founder Effect
Gene Expression
Myoclonus

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

Myoclonic Epilepsy
Genes
Founder Effect
Gene Expression
Myoclonus

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

Myoclonic Epilepsy
Genes
Founder Effect
Gene Expression
Myoclonus

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

Myoclonic Epilepsy
Genes
Founder Effect
Gene Expression
Myoclonus

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

Partial Epilepsy
Sirolimus
Mutation
Exome
Genes

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

Tremor
Psychiatry
Comorbidity
Juvenile Myoclonic Epilepsy
Anxiety
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

Ceroid
Neuronal Ceroid-Lipofuscinoses
Mutation
Lysosomal Storage Diseases
Neurologic Manifestations

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

Progressive Myoclonic Epilepsy
Mutation
Exome
Voltage-Gated Potassium Channels
Myoclonus

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

Frontal Lobe Epilepsy
Sudden Death
Epilepsy
Cohort Studies
Incidence

Prevalence of nocturnal frontal lobe epilepsy in the adult population of Bologna and Modena, Emilia-Romagna region, Italy

Vignatelli, L., Bisulli, F., Giovannini, G., Licchetta, L., Naldi, I., Mostacci, B., Rubboli, G., Provini, F. & Tinuper, P., Mar 1 2015, In : Sleep. 38, 3, p. 479-485 7 p.

Research output: Contribution to journalArticle

Frontal Lobe Epilepsy
Italy
Population
Epilepsy
Rare Diseases
2014

Auditory aura in nocturnal frontal lobe epilepsy: A red flag to suspect an extra-frontal epileptogenic zone

Ferri, L., Bisulli, F., Nobili, L., Tassi, L., Licchetta, L., Mostacci, B., Stipa, C., Mainieri, G., Bernabè, G., Provini, F. & Tinuper, P., Nov 1 2014, In : Sleep Medicine. 15, 11, p. 1417-1423 7 p.

Research output: Contribution to journalArticle

Frontal Lobe Epilepsy
Epilepsy
Temporal Lobe
Seizures
Auditory Cortex

Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11-q13.31

Bisulli, F., Naldi, I., Baldassari, S., Magini, P., Licchetta, L., Castegnaro, G., Fabbri, M., Stipa, C., Ferrari, S., Seri, M., Gonçalves Silva, G. E., Tinuper, P. & Pippucci, T., 2014, In : Epilepsia. 55, 6, p. 841-848 8 p.

Research output: Contribution to journalArticle

Single Nucleotide Polymorphism
Chromosomes
Haplotypes
Epilepsy
Seizures

LGI1 microdeletions are not a frequent cause of partial epilepsy with auditory features (PEAF)

Magini, P., Bisulli, F., Baldassari, S., Stipa, C., Naldi, I., Licchetta, L., Menghi, V., Tinuper, P., Seri, M. & Pippucci, T., 2014, In : Epilepsy Research. 108, 5, p. 972-977 6 p.

Research output: Contribution to journalArticle

Leucine
Glioma
Genes
Genetic Heterogeneity
Multiplex Polymerase Chain Reaction

Limbic encephalitis with anti-GAD antibodies and Thomsen myotonia: A casual or causal association?

Licchetta, L., Bisulli, F., Naldi, I., Mainieri, G. & Tinuper, P., Sep 1 2014, In : Epileptic Disorders. 16, 3, p. 362-365 4 p.

Research output: Contribution to journalArticle

Limbic Encephalitis
Myotonia
Anti-Idiotypic Antibodies
Epilepsy
Mutation

Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations

Scheffer, I. E., Heron, S. E., Regan, B. M., Mandelstam, S., Crompton, D. E., Hodgson, B. L., Licchetta, L., Provini, F., Bisulli, F., Vadlamudi, L., Gecz, J., Connelly, A., Tinuper, P., Ricos, M. G., Berkovic, S. F. & Dibbens, L. M., 2014, In : Annals of Neurology. 75, 5, p. 782-787 6 p.

Research output: Contribution to journalArticle

Partial Epilepsy
Sirolimus
Mutation
Brain
Tuberous Sclerosis

Tailored surgery for drug-resistant epilepsy due to temporal pole encephalocele and microdysgenesis

Giulioni, M., Licchetta, L., Bisulli, F., Rubboli, G., Mostacci, B., Marucci, G., Martinoni, M., Ferri, L., Volpi, L., Calbucci, F., Baruzzi, A. & Tinuper, P., Feb 2014, In : Seizure. 23, 2, p. 164-166 3 p.

Research output: Contribution to journalArticle

2013

A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype

Licchetta, L., Pippucci, T., Bisulli, F., Cantalupo, G., Magini, P., Alvisi, L., Baldassari, S., Martinelli, P., Naldi, I., Vanni, N., Liguori, R., Seri, M. & Tinuper, P., Jul 2013, In : Epilepsia. 54, 7, p. 1298-1306 9 p.

Research output: Contribution to journalArticle

Pedigree
Haplotypes
Tremor
Seizures
Chromosomes

Erratum: A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype (Epilepsia (2013) 54 (1298-1306))

Licchetta, L., Pippucci, T., Bisulli, F., Cantalupo, G., Magini, P., Alvisi, L., Baldassari, S., Martinelli, P., Naldi, I., Vanni, N., Liguori, R., Seri, M. & Tinuper, P., Sep 2013, In : Epilepsia. 54, 9, p. 1709 1 p.

Research output: Contribution to journalArticle

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

Dibbens, L. M., De Vries, B., Donatello, S., Heron, S. E., Hodgson, B. L., Chintawar, S., Crompton, D. E., Hughes, J. N., Bellows, S. T., Klein, K. M., Callenbach, P. M. C., Corbett, M. A., Gardner, A. E., Kivity, S., Iona, X., Regan, B. M., Weller, C. M., Crimmins, D., O'Brien, T. J., Guerrero-López, R. & 15 others, Mulley, J. C., Dubeau, F., Licchetta, L., Bisulli, F., Cossette, P., Thomas, P. Q., Gecz, J., Serratosa, J., F Brouwer, O., Andermann, F., Andermann, E., Van Den Maagdenberg, A. M. J. M., Pandolfo, M., Berkovic, S. F. & Scheffer, I. E., May 2013, In : Nature Genetics. 45, 5, p. 546-551 6 p.

Research output: Contribution to journalArticle

Partial Epilepsy
Mutation
Seizures
Exome
Brain

Tobacco habits in nocturnal frontal lobe epilepsy

Naldi, I., Bisulli, F., Vignatelli, L., Licchetta, L., Pittau, F., Di Vito, L., Mostacci, B., Menghi, V., Provini, F., Montagna, P. & Tinuper, P., Jan 2013, In : Epilepsy and Behavior. 26, 1, p. 114-117 4 p.

Research output: Contribution to journalArticle

Frontal Lobe Epilepsy
Tobacco Use
Habits
Tobacco
Arousal