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Research Output 2008 2020

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Article
2019
Brain Diseases
Nervous System Malformations
Exome
Mutation
Intellectual Disability

Generalized tonic seizures with autonomic signs are the hallmark of SCN8A developmental and epileptic encephalopathy

Trivisano, M., Pavia, G. C., Ferretti, A., Fusco, L., Vigevano, F. & Specchio, N., Jul 2019, In : Epilepsy and Behavior. 96, p. 219-223 5 p.

Research output: Contribution to journalArticle

Brain Diseases
Seizures
Cyanosis
Tachycardia
Epilepsy
Cannabidiol
Brain Diseases
Epilepsy
Pediatrics
Seizures
2018

A single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletion

Nardella, G., Visci, G., Guarnieri, V., Castellana, S., Biagini, T., Bisceglia, L., Palumbo, O., Trivisano, M., Vaira, C., Scerrati, M., Debrasi, D., D'Angelo, V., Carella, M., Merla, G., Mazza, T., Castori, M., D'Agruma, L. & Fusco, C., Aug 30 2018, In : Human Mutation.

Research output: Contribution to journalArticle

Central Nervous System Cavernous Hemangioma
Penetrance
Autophagy
Computer Simulation
Genes

A single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletion

Nardella, G., Visci, G., Guarnieri, V., Castellana, S., Biagini, T., Bisceglia, L., Palumbo, O., Trivisano, M., Vaira, C., Scerrati, M., Debrasi, D., D'Angelo, V., Carella, M., Merla, G., Mazza, T., Castori, M., D'Agruma, L. & Fusco, C., Dec 1 2018, In : Human Mutation. 39, 12, p. 1885-1900 16 p.

Research output: Contribution to journalArticle

Central Nervous System Cavernous Hemangioma
Penetrance
Autophagy
Computer Simulation
Genes

CHD2-epilepsy: Polygraphic documentation of self-induced seizures due to fixation-off sensitivity

Caputo, D., Trivisano, M., Vigevano, F. & Fusco, L., Apr 2018, In : Seizure. 57, p. 8-10 3 p.

Research output: Contribution to journalArticle

Documentation
Epilepsy
Seizures
Myoclonic Epilepsy
Phenotype

Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry

EURAP Study Group, Jun 1 2018, In : The Lancet Neurology. 17, 6, p. 530-538 9 p.

Research output: Contribution to journalArticle

etiracetam
Anticonvulsants
Registries
Cohort Studies
Prospective Studies

Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study

Trivisano, M., Pietrafusa, N., Terracciano, A., Marini, C., Mei, D., Darra, F., Accorsi, P., Battaglia, D., Caffi, L., Canevini, M. P., Cappelletti, S., Cesaroni, E., de Palma, L., Costa, P., Cusmai, R., Giordano, L., Ferrari, A., Freri, E., Fusco, L., Granata, T. & 20 others, Martino, T., Mastrangelo, M., Bova, S. M., Parmeggiani, L., Ragona, F., Sicca, F., Striano, P., Specchio, L. M., Tondo, I., Zambrelli, E., Zamponi, N., Zanus, C., Boniver, C., Vecchi, M., Avolio, C., Dalla Bernardina, B., Bertini, E., Guerrini, R., Vigevano, F. & Specchio, N., Dec 2018, In : Epilepsia. 59, 12, p. 2260-2271 12 p.

Research output: Contribution to journalArticle

Multicenter Studies
Epilepsy
Seizures
Phenotype
Intellectual Disability

Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study

Trivisano, M., Pietrafusa, N., Terracciano, A., Marini, C., Mei, D., Darra, F., Accorsi, P., Battaglia, D., Caffi, L., Canevini, M. P., Cappelletti, S., Cesaroni, E., de Palma, L., Costa, P., Cusmai, R., Giordano, L., Ferrari, A., Freri, E., Fusco, L., Granata, T. & 20 others, Martino, T., Mastrangelo, M., Bova, S. M., Parmeggiani, L., Ragona, F., Sicca, F., Striano, P., Specchio, L. M., Tondo, I., Zambrelli, E., Zamponi, N., Zanus, C., Boniver, C., Vecchi, M., Avolio, C., Dalla Bernardina, B., Bertini, E., Guerrini, R., Vigevano, F. & Specchio, N., Dec 1 2018, In : Epilepsia. 59, 12, p. 2260-2271 12 p.

Research output: Contribution to journalArticle

Multicenter Studies
Epilepsy
Seizures
Phenotype
Intellectual Disability

Defining the phenotypic spectrum of SLC6A1 mutations

Johannesen, K. M., Gardella, E., Linnankivi, T., Courage, C., de Saint Martin, A., Lehesjoki, A-E., Mignot, C., Afenjar, A., Lesca, G., Abi-Warde, M-T., Chelly, J., Piton, A., Merritt, J. L., Rodan, L. H., Tan, W-H., Bird, L. M., Nespeca, M., Gleeson, J. G., Yoo, Y., Choi, M. & 32 others, Chae, J-H., Czapansky-Beilman, D., Reichert, S. C., Pendziwiat, M., Verhoeven, J. S., Schelhaas, H. J., Devinsky, O., Christensen, J., Specchio, N., Trivisano, M., Weber, Y. G., Nava, C., Keren, B., Doummar, D., Schaefer, E., Hopkins, S., Dubbs, H., Shaw, J. E., Pisani, L., Myers, C. T., Tang, S., Tang, S., Pal, D. K., Millichap, J. J., Carvill, G. L., Helbig, K. L., Mecarelli, O., Striano, P., Helbig, I., Rubboli, G., Mefford, H. C. & Møller, R. S., Feb 2018, In : Epilepsia. 59, 2, p. 389-402 14 p.

Research output: Contribution to journalArticle

Intellectual Disability
Generalized Epilepsy
Mutation
Myoclonic Epilepsy
Epilepsy

The phenotype of SCN8A developmental and epileptic encephalopathy

Gardella, E., Marini, C., Trivisano, M., Fitzgerald, M. P., Alber, M., Howell, K. B., Darra, F., Siliquini, S., Bölsterli, B. K., Masnada, S., Pichiecchio, A., Johannesen, K. M., Jepsen, B., Fontana, E., Anibaldi, G., Russo, S., Cogliati, F., Montomoli, M., Specchio, N., Rubboli, G. & 8 others, Veggiotti, P., Beniczky, S., Wolff, M., Helbig, I., Vigevano, F., Scheffer, I. E., Guerrini, R. & Møller, R. S., Sep 18 2018, In : Neurology. 91, 12, p. e1112-e1124

Research output: Contribution to journalArticle

Brain Diseases
Seizures
Phenotype
Electroencephalography
Cortical Blindness

The phenotype of SCN8A developmental and epileptic encephalopathy

Gardella, E., Marini, C., Trivisano, M., Fitzgerald, M. P., Alber, M., Howell, K. B., Darra, F., Siliquini, S., Bölsterli, B. K., Masnada, S., Pichiecchio, A., Johannesen, K. M., Jepsen, B., Fontana, E., Anibaldi, G., Russo, S., Cogliati, F., Montomoli, M., Specchio, N., Rubboli, G. & 8 others, Veggiotti, P., Beniczky, S., Wolff, M., Helbig, I., Vigevano, F., Scheffer, I. E., Guerrini, R. & Møller, R. S., Sep 18 2018, In : Neurology. 91, 12, p. e1112-e1124

Research output: Contribution to journalArticle

Brain Diseases
Phenotype
Electroencephalography
Seizures
Cortical Blindness

The phenotype of SCN8A developmental and epileptic encephalopathy

Gardella, E., Marini, C., Trivisano, M., Fitzgerald, M. P., Alber, M., Howell, K. B., Darra, F., Siliquini, S., Bölsterli, B. K., Masnada, S., Pichiecchio, A., Johannesen, K. M., Jepsen, B., Fontana, E., Anibaldi, G., Russo, S., Cogliati, F., Montomoli, M., Specchio, N., Rubboli, G. & 8 others, Veggiotti, P., Beniczky, S., Wolff, M., Helbig, I., Vigevano, F., Scheffer, I. E., Guerrini, R. & Møller, R. S., Sep 18 2018, In : Neurology. 91, 12, p. e1112-e1124

Research output: Contribution to journalArticle

2017

Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations

Cetica, V., Chiari, S., Mei, D., Parrini, E., Grisotto, L., Marini, C., Pucatti, D., Ferrari, A., Sicca, F., Specchio, N., Trivisano, M., Battaglia, D., Contaldo, I., Zamponi, N., Petrelli, C., Granata, T., Ragona, F., Avanzini, G. & Guerrini, R., Mar 14 2017, In : Neurology. 88, 11, p. 1037-1044 8 p.

Research output: Contribution to journalArticle

Myoclonic Epilepsy
Seizures
Mutation
ROC Curve
Febrile Seizures

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Wolff, M., Johannesen, K. M., Hedrich, U. B. S., Masnada, S., Rubboli, G., Gardella, E., Lesca, G., Ville, D., Milh, M., Villard, L., Afenjar, A., Chantot-Bastaraud, S., Mignot, C., Lardennois, C., Nava, C., Schwarz, N., Gérard, M., Perrin, L., Doummar, D., Auvin, S. & 30 others, Miranda, M. J., Hempel, M., Brilstra, E., Knoers, N., Verbeek, N., van Kempen, M., Braun, K. P., Mancini, G., Biskup, S., Hörtnagel, K., Döcker, M., Bast, T., Loddenkemper, T., Wong-Kisiel, L., Baumeister, F. M., Fazeli, W., Striano, P., Dilena, R., Fontana, E., Zara, F., Kurlemann, G., Klepper, J., Thoene, J. G., Arndt, D. H., Deconinck, N., Schmitt-Mechelke, T., Maier, O., Muhle, H., Trivisano, M. & Specchio, N., May 1 2017, In : Brain. 140, 5, p. 1316-1336 21 p.

Research output: Contribution to journalArticle

Genetic Heterogeneity
NAV1.2 Voltage-Gated Sodium Channel
Epilepsy
Brain Diseases
Phenotype

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Wolff, M., Johannesen, K. M., Hedrich, U. B. S., Masnada, S., Rubboli, G., Gardella, E., Lesca, G., Ville, D., Milh, M., Villard, L., Afenjar, A., Chantot-Bastaraud, S., Mignot, C., Lardennois, C., Nava, C., Schwarz, N., Gérard, M., Perrin, L., Doummar, D., Auvin, S. & 65 others, Miranda, M. J., Hempel, M., Brilstra, E., Knoers, N., Verbeek, N., Van Kempen, M., Braun, K. P., Mancini, G., Biskup, S., Hörtnagel, K., Döcker, M., Bast, T., Loddenkemper, T., Wong-Kisiel, L., Baumeister, F. M., Fazeli, W., Striano, P., Dilena, R., Fontana, E., Zara, F., Kurlemann, G., Klepper, J., Thoene, J. G., Arndt, D. H., Deconinck, N., Schmitt-Mechelke, T., Maier, O., Muhle, H., Wical, B., Finetti, C., Brückner, R., Pietz, J., Golla, G., Jillella, D., Linnet, K. M., Charles, P., Moog, U., Õiglane-Shlik, E., Mantovani, J. F., Park, K., Deprez, M., Lederer, D., Mary, S., Scalais, E., Selim, L., Van Coster, R., Lagae, L., Nikanorova, M., Hjalgrim, H., Korenke, G. C., Trivisano, M., Specchio, N., Ceulemans, B., Dorn, T., Helbig, K. L., Hardies, K., Stamberger, H., De Jonghe, P., Weckhuysen, S., Lemke, J. R., Krägeloh-Mann, I., Helbig, I., Kluger, G., Lerche, H. & Møller, R. S., May 1 2017, In : Brain. 140, 5, p. 1316-1336 21 p.

Research output: Contribution to journalArticle

Genetic Heterogeneity
Sodium Channel Blockers
Epilepsy
Mutation
Seizures

Long-term applicability of the new ILAE definition of epilepsy. Results from the PRO-LONG study

Beretta, S., Carone, D., Zanchi, C., Bianchi, E., Pirovano, M., Trentini, C., Padovano, G., Colombo, M., Cereda, D., Scanziani, S., Giussani, G., Gasparini, S., Bogliun, G., Ferrarese, C., Beghi, E., Romeo, A., Viri, M., Lodi, M., Specchio, L., Trivisano, M. & 23 others, Mecarelli, O., Zarabla, A., Capovilla, G., Beccaria, F., Sasanelli, F., Andrea Galimberti, C., Tartara, E., Zamponi, N., Cappanera, S., Aguglia, U., Pustorino, G., Ferlazzo, E., La Neve, A., Luisi, C., Pontrelli, G., Basso, P., Pozzi, A., Cantisani, A. T., Papetti, R., De Maria, G., DiFrancesco, J. C., Albanese, Y. & the PRO-LONG Study Group, Sep 1 2017, In : Epilepsia. 58, 9, p. 1518-1523 6 p.

Research output: Contribution to journalArticle

Epilepsy
Seizures
Recurrence
Neurologic Examination
Neuroimaging

Photosensitivity is an early marker of neuronal ceroid lipofuscinosis type 2 disease

Specchio, N., Bellusci, M., Pietrafusa, N., Trivisano, M., de Palma, L. & Vigevano, F., Aug 1 2017, In : Epilepsia. 58, 8, p. 1380-1388 9 p.

Research output: Contribution to journalArticle

Ceroid
Magnetic Resonance Imaging
Atrophy
Seizures
Ceroid Lipofuscinosis, Neuronal, 2

Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features

Niturad, C. E., Lev, D., Kalscheuer, V. M., Charzewska, A., Schubert, J., Lerman-Sagie, T., Kroes, H. Y., Oegema, R., Traverso, M., Specchio, N., Lassota, M., Chelly, J., Bennett-Back, O., Carmi, N., Koffler-Brill, T., Iacomino, M., Trivisano, M., Capovilla, G., Striano, P., Nawara, M. & 19 others, Rzoca, S., Fischer, U., Bienek, M., Jensen, C., Hu, H., Thiele, H., Altmüller, J., Krause, R., May, P., Becker, F., Balling, R., Biskup, S., Haas, S. A., Nürnberg, P., Van Gassen, K. L. I., Lerche, H., Zara, F., Maljevic, S. & Leshinsky-Silver, E., Nov 1 2017, In : Brain. 140, 11, p. 2879-2894 16 p.

Research output: Contribution to journalArticle

Brain Diseases
Epilepsy
Genes
Mutation
GABA-A Receptors

Reduced steroidogenesis in patients with PCDH19-female limited epilepsy

Trivisano, M., Lucchi, C., Rustichelli, C., Terracciano, A., Cusmai, R., Ubertini, G. M., Giannone, G., Bertini, E. S., Vigevano, F., Gecz, J., Biagini, G. & Specchio, N., Jun 1 2017, In : Epilepsia. 58, 6, p. e91-e95

Research output: Contribution to journalArticle

Pregnanolone
Progesterone
Epilepsy
Adrenocorticotropic Hormone
Hydrocortisone
2016

Intravenous lacosamide in seizure emergencies: Observations from a hospitalized in-patient adult population

d'Orsi, G., Pascarella, M. G., Martino, T., Carapelle, E., Pacillo, F., Di Claudio, M. T., Mancini, D., Trivisano, M., Avolio, C. & Specchio, L. M., Nov 1 2016, In : Seizure. 42, p. 20-28 9 p.

Research output: Contribution to journalArticle

Seizures
Emergencies
Status Epilepticus
Population
lacosamide
Missense Mutation
Ataxia
Migraine Disorders
Cerebellar Diseases
Mutation
Myoclonic Epilepsy
Epilepsy
Fever
Medical Records
Students
Epilepsy
Point Mutation
Seizures
X-Linked Genes
Mutation
2015

Acute intralesional recording in hypothalamic hamartoma: description of 4 cases

Specchio, N., Rizzi, M., Trivisano, M., Fusco, L., Rebessi, E., Cappelletti, S., De Palma, L., Villani, F., Savioli, A., De Benedictis, A., Marras, C. E., Vigevano, F. & Delalande, O., Sep 24 2015, In : Acta Neurologica Belgica. 115, 3, p. 233-239 7 p.

Research output: Contribution to journalArticle

Electroencephalography
Scalp
Partial Epilepsy
Seizures
Stroke

Bilateral putaminal necrosis and bronopol toxicity

Trivisano, M., Carapelle, E., Martino, T. & Specchio, L. M., Feb 19 2015, In : BMJ Case Reports. 2015

Research output: Contribution to journalArticle

formic acid
Methanol
Necrosis
Alcoholic Intoxication
Local Anti-Infective Agents
Induced Pluripotent Stem Cells
Neurogenesis
Stem Cells
Neurons
Cadherins

CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures

Trivisano, M., Striano, P., Sartorelli, J., Giordano, L., Traverso, M., Accorsi, P., Cappelletti, S., Claps, D. J., Vigevano, F., Zara, F. & Specchio, N., Oct 1 2015, In : Epilepsy and Behavior. 51, p. 53-56 4 p.

Research output: Contribution to journalArticle

Myoclonic Epilepsy
Generalized Epilepsy
Seizures
Mutation
Intellectual Disability
Intellectual Disability
Epilepsy
Seizures
Genes
Language Development Disorders
Epilepsy
Myoclonic Epilepsy
Valproic Acid
Anticonvulsants
Clinical Trials
Temporal Lobe Epilepsy
Vomiting
Electroencephalography
Stroke
Seizures
Nicotinic Receptors
Epilepsy
Seizures
Phenotype
Mutation

Peri-ictal water drinking: A rare automatic behaviour in temporal lobe epilepsy

Pietrafusa, N., Trivisano, M., De Palma, L., Serino, D., Moavero, R., Benvenga, A., Cappelletti, S., Boero, G., Vigevano, F., La Neve, A. & Specchio, N., Dec 1 2015, In : Epileptic Disorders. 17, 4, p. 384-396 13 p.

Research output: Contribution to journalArticle

Temporal Lobe Epilepsy
Drinking Water
Stroke
Automatism
Seizures
2014

Lacosamide in absence status epilepticus

D'Orsi, G., Pacillo, F., Trivisano, M., Pascarella, M. G., Ferrara, M. A. & Specchio, L. M., 2014, In : Seizure. 23, 5, p. 397-398 2 p.

Research output: Contribution to journalArticle

Lentiform fork sign: A magnetic resonance finding in a case of acute metabolic acidosis

Grasso, D., Borreggine, C., Perfetto, F., Bertozzi, V., Trivisano, M., Specchio, L. M., Grilli, G. & Macarini, L., 2014, In : Neuroradiology Journal. 27, 3, p. 288-292 5 p.

Research output: Contribution to journalArticle

Acidosis
Stupor
Edema
Magnetic Resonance Spectroscopy
Necrosis
Myoclonic Epilepsy
Photic Stimulation
Seizures
Temporal Lobe
Beginning of Human Life
2013

Brain SPECT imaging of ictal smile seizure

Modoni, S., Urbano, N., Trivisano, M., Pascarella, M. G., D'Orsi, G., Di Claudio, T. & Specchio, L. M., Mar 11 2013, (Accepted/In press) In : Clinical Nuclear Medicine.

Research output: Contribution to journalArticle

Single-Photon Emission-Computed Tomography
Neuroimaging
Happiness
Seizures
Stroke

Brain SPECT imaging of ictal smile seizure.

Modoni, S., Urbano, N., Trivisano, M., Pascarella, M. G., D'Orsi, G., Di Claudio, T. & Specchio, L. M., May 2013, In : Clinical Nuclear Medicine. 38, 5

Research output: Contribution to journalArticle

Single-Photon Emission-Computed Tomography
Neuroimaging
Happiness
Seizures
Stroke

Efficacia della lacosamide nello stato epilettico focale motorio: Studio clinico e video-poligrafico

Translated title of the contribution: Efficacy of intravenous lacosamide in symptomatic focal motor status epilepticus: A clinical and video-polygraphic studyTrivisano, M., D'Orsi, G., Pascarella, M. G., Ferrara, M., Pacillo, F., Luisi, C., Carapelle, E., Di Claudio, M. T. & Specchio, L. M., Apr 2013, In : Bollettino - Lega Italiana contro l'Epilessia. 145, p. 284-286 3 p.

Research output: Contribution to journalArticle

Status Epilepticus
Seizures
Aphasia
Therapeutics
Neuroepithelial Neoplasms

Partial Trisomy 18q and Epileptic Spasms Induced by Eating Associated With Bilateral Opercular Dysplasia

D'Orsi, G., Pascarella, M. G., Pansini, A., Buonadonna, A. L., Trivisano, M., Pacillo, F., Carapelle, E., Demaio, V., Minervini, M., Gentile, M. & Specchio, L. M., May 2013, In : American Journal of Medical Genetics, Part A. 161, 5, p. 1194-1195 2 p.

Research output: Contribution to journalArticle

Seizures
Proteins
Mutation
Epilepsy
Carbamazepine

Stato epilettico focale frontale "da paura": Correlazioni EEG - SPECT

Translated title of the contribution: Fear as nonconvulsive status epilepticus of frontal origin: EEG-SPECT correlationPacillo, F., D'Orsi, G., Pascarella, M. G., Trivisano, M., Di Claudio, M. T., Luisi, C., Boero, G., Grilli, G., Modoni, S. & Specchio, L. M., Apr 2013, In : Bollettino - Lega Italiana contro l'Epilessia. 145, p. 247-250 4 p.

Research output: Contribution to journalArticle

Status Epilepticus
Single-Photon Emission-Computed Tomography
Fear
Electroencephalography
Occipital Lobe
2012

Electroencephalographic features in Dravet syndrome: Five-year follow-up study in 22 patients

Specchio, N., Balestri, M., Trivisano, M., Japaridze, N., Striano, P., Carotenuto, A., Cappelletti, S., Specchio, L. M., Fusco, L. & Vigevano, F., Apr 2012, In : Journal of Child Neurology. 27, 4, p. 439-444 6 p.

Research output: Contribution to journalArticle

Myoclonic Epilepsy
Electroencephalography
Voltage-Gated Sodium Channels
Mutation

Epilepsy in ring 14 chromosome syndrome

Specchio, N., Trivisano, M., Serino, D., Cappelletti, S., Carotenuto, A., Claps, D., Marras, C. E., Fusco, L., Elia, M. & Vigevano, F., Dec 2012, In : Epilepsy and Behavior. 25, 4, p. 585-592 8 p.

Research output: Contribution to journalArticle

Epilepsy
Seizures
Electroencephalography
Muscle Hypotonia
Motor Skills

Epileptic seizures, movement disorders, and breathing disturbances in Rett syndrome: Diagnostic relevance of video-polygraphy

D'Orsi, G., Trivisano, M., Luisi, C., Demaio, V., Di Claudio, M. T., Pascarella, M. G., Sciruicchio, V., Galeone, D., La Neve, A., Scarpelli, F., Calvario, T., Minervini, M., La Selva, L. & Specchio, L. M., Nov 2012, In : Epilepsy and Behavior. 25, 3, p. 401-407 7 p.

Research output: Contribution to journalArticle

Rett Syndrome
Movement Disorders
Epilepsy
Respiration
Seizures

Fear as nonconvulsive status epilepticus of frontal origin: EEG-SPECT correlation

d'Orsi, G., Pacillo, F., Trivisano, M., Pascarella, M. G., Luisi, C., Di Claudio, M. T., Boero, G., Grilli, G., Modoni, S. & Specchio, L. M., Jun 2012, In : Epilepsy and Behavior. 24, 2, p. 288-289 2 p.

Research output: Contribution to journalArticle

Lacosamide: Tollerabilità ed efficacia nelle prime esperienze di utilizzo nella pratica clinica

Translated title of the contribution: Lacosamide: Tolerability and efficacy in early experiences of use in clinical practiceFerrara, M. S., D'Orsi, G., Trivisano, M., Pascarella, M. G., Carapelle, E., Grasso, R. & Specchio, L. M., May 2012, In : Bollettino - Lega Italiana contro l'Epilessia. 144, p. 198-201 4 p.

Research output: Contribution to journalArticle

Ataxia
Diplopia
Sodium Channels
Sleep Stages
Vertigo

Neonatal hemifacial spasm and fourth ventricle mass

Specchio, N., Trivisano, M., Bernardi, B., Marras, C. E., Faggioli, R., Fiumana, E., Cappelletti, S., Delalande, O., Vigevano, F. & Fusco, L., Aug 2012, In : Developmental Medicine and Child Neurology. 54, 8, p. 697-703 7 p.

Research output: Contribution to journalArticle

Hemifacial Spasm
Fourth Ventricle
Electroencephalography
Stroke
Blinking

Studio video-poligrafico nella sindrome delle assenze con mioclonie periorali

Translated title of the contribution: Ictal video-polygraphic features of perioral myoclonia with absencesTrivisano, M., D'Orsi, G., Pascarella, M. G., Carapelle, E., Grasso, R., Demaio, V. & Specchio, L. M., May 2012, In : Bollettino - Lega Italiana contro l'Epilessia. 144, p. 122-124 3 p.

Research output: Contribution to journalArticle

Electromyography
Electroencephalography
Stroke
Central Pattern Generators
Automatism