Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 253

1.

Distortion of the cortical motor map in patients with Unverricht-Lundborg disease: A combined TMS-MRI study.

Rossi Sebastiano D, Visani E, Contarino VE, Panzica F, Duran D, D'Incerti L, Franceschetti S, Canafoglia L.

Epilepsy Res. 2020 Feb;160:106278. doi: 10.1016/j.eplepsyres.2020.106278. Epub 2020 Jan 15.

PMID:
31954920
2.

Advances in genetic testing and optimization of clinical management in children and adults with epilepsy.

Scala M, Bianchi A, Bisulli F, Coppola A, Elia M, Trivisano M, Pruna D, Pippucci T, Canafoglia L, Lattanzi S, Franceschetti S, Nobile C, Gambardella A, Michelucci R, Zara F, Striano P.

Expert Rev Neurother. 2020 Mar;20(3):251-269. doi: 10.1080/14737175.2020.1713101. Epub 2020 Jan 27.

PMID:
31941393
3.

Connectivity measures suggest a sub-cortical generator of myoclonus in Angelman syndrome.

Ferlazzo E, Franceschetti S, Gasparini S, Elia M, Canafoglia L, Pantaleoni C, Ascoli M, D'Agostino T, Sueri C, Ferrigno G, Panzica F, Cianci V, Aguglia U.

Clin Neurophysiol. 2019 Dec;130(12):2231-2237. doi: 10.1016/j.clinph.2019.08.031. Epub 2019 Oct 24.

PMID:
31704627
4.

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

Corbett MA, Kroes T, Veneziano L, Bennett MF, Florian R, Schneider AL, 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 AF, 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 KL, 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 JW, Afawi Z, Helbig I, Ishiura H, Tsuji S, Sisodiya SM, Casari G, Sadleir LG, van Coller R, Tijssen MAJ, Klein KM, van den Maagdenberg AMJM, Zara F, Guerrini R, Berkovic SF, Pippucci T, Canafoglia L, Bahlo M, Striano P, Scheffer IE, Brancati F, Depienne C, Gecz J.

Nat Commun. 2019 Oct 29;10(1):4920. doi: 10.1038/s41467-019-12671-y.

5.

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, Gambardella A, Di Bonaventura C, Michelucci R, Granata T, Bisulli F, Licchetta L, Tinuper P, Beccaria F, Visani E, Franceschetti S.

Epilepsy Res. 2019 Oct;156:106191. doi: 10.1016/j.eplepsyres.2019.106191. Epub 2019 Aug 16.

PMID:
31446282
6.

Gamma electroencephalographic coherence and theory of mind in healthy subjects.

Panzica F, Schiaffi E, Visani E, Franceschetti S, Giovagnoli AR.

Epilepsy Behav. 2019 Nov;100(Pt B):106435. doi: 10.1016/j.yebeh.2019.07.036. Epub 2019 Aug 17. Review.

PMID:
31427268
7.

Early clinical and EEG findings associated with the outcome in childhood absence epilepsy.

Canafoglia L, Dettori MS, Duran D, Ragona F, Freri E, Casellato S, Granata T, Franceschetti S, Panzica F.

Epilepsy Behav. 2019 Sep;98(Pt A):273-278. doi: 10.1016/j.yebeh.2019.06.040. Epub 2019 Aug 13.

PMID:
31419648
8.

Higher order spectral analysis of scalp EEG activity reveals non-linear behavior during rhythmic visual stimulation.

Coelli S, Tacchino G, Visani E, Panzica F, Franceschetti S, Bianchi AM.

J Neural Eng. 2019 Sep 17;16(5):056028. doi: 10.1088/1741-2552/ab296e.

PMID:
31189136
9.

Epileptic phenotypes in children with early-onset mitochondrial diseases.

Matricardi S, Canafoglia L, Ardissone A, Moroni I, Ragona F, Ghezzi D, Lamantea E, Nardocci N, Franceschetti S, Granata T.

Acta Neurol Scand. 2019 Sep;140(3):184-193. doi: 10.1111/ane.13130. Epub 2019 Jun 6.

PMID:
31102535
10.

HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature.

DiFrancesco JC, Castellotti B, Milanesi R, Ragona F, Freri E, Canafoglia L, Franceschetti S, Ferrarese C, Magri S, Taroni F, Costa C, Labate A, Gambardella A, Solazzi R, Binda A, Rivolta I, Di Gennaro G, Casciato S, D'Incerti L, Barbuti A, DiFrancesco D, Granata T, Gellera C.

Epilepsy Res. 2019 Jul;153:49-58. doi: 10.1016/j.eplepsyres.2019.04.004. Epub 2019 Apr 8. Review.

PMID:
30986657
11.

Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypes.

Castellotti B, Ragona F, Freri E, Solazzi R, Ciardullo S, Tricomi G, Venerando A, Salis B, Canafoglia L, Villani F, Franceschetti S, Nardocci N, Gellera C, DiFrancesco JC, Granata T.

J Neurol. 2019 Jun;266(6):1439-1448. doi: 10.1007/s00415-019-09280-6. Epub 2019 Mar 20.

PMID:
30895386
12.

Different patterns of movement-related cortical oscillations in patients with myoclonus and in patients with spinocerebellar ataxia.

Visani E, Mariotti C, Nanetti L, Mongelli A, Castaldo A, Panzica F, Franceschetti S, Canafoglia L.

Clin Neurophysiol. 2019 May;130(5):714-721. doi: 10.1016/j.clinph.2019.01.021. Epub 2019 Feb 16.

PMID:
30889419
13.

DNA damage and transcriptional regulation in iPSC-derived neurons from Ataxia Telangiectasia patients.

Corti A, Sota R, Dugo M, Calogero RA, Terragni B, Mantegazza M, Franceschetti S, Restelli M, Gasparini P, Lecis D, Chrzanowska KH, Delia D.

Sci Rep. 2019 Jan 24;9(1):651. doi: 10.1038/s41598-018-36912-0.

14.

Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation.

Canafoglia L, Castellotti B, Ragona F, Freri E, Granata T, Chiapparini L, Gellera C, Scaioli V, Franceschetti S, DiFrancesco JC.

Seizure. 2019 Feb;65:106-108. doi: 10.1016/j.seizure.2019.01.005. Epub 2019 Jan 8. No abstract available.

15.

GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary results.

Bersano A, Bedini G, Nava S, Acerbi F, Sebastiano DR, Binelli S, Franceschetti S, Faragò G, Grisoli M, Gioppo A, Ferroli P, Bruzzone MG, Riva D, Ciceri E, Pantaleoni C, Saletti V, Esposito S, Nardocci N, Zibordi F, Caputi L, Marzoli SB, Zedde ML, Pavanello M, Raso A, Capra V, Pantoni L, Sarti C, Pezzini A, Caria F, Dell' Acqua ML, Zini A, Baracchini C, Farina F, Sanguigni S, De Lodovici ML, Bono G, Capone F, Di Lazzaro V, Lanfranconi S, Toscano M, Di Piero V, Sacco S, Carolei A, Toni D, Paciaroni M, Caso V, Perrone P, Calloni MV, Romani A, Cenzato M, Fratianni A, Ciusani E, Prontera P, Lasserve ET, Blecharz K, Vajkoczy P, Parati EA; GEN-O-MA study group.

Neurol Sci. 2019 Mar;40(3):561-570. doi: 10.1007/s10072-018-3664-z. Epub 2019 Jan 3.

PMID:
30604336
16.

Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.

Berkovic SF, Oliver KL, Canafoglia L, Krieger P, Damiano JA, Hildebrand MS, Morbin M, Vears DF, Sofia V, Giuliano L, Garavaglia B, Simonati A, Santorelli FM, Gambardella A, Labate A, Belcastro V, Castellotti B, Ozkara C, Zeman A, Rankin J, Mole SE, Aguglia U, Farrell M, Rajagopalan S, McDougall A, Brammah S, Andermann F, Andermann E, Dahl HM, Franceschetti S, Carpenter S.

Brain. 2019 Jan 1;142(1):59-69. doi: 10.1093/brain/awy297.

PMID:
30561534
17.

ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype.

Nanetti L, Sarto E, Castaldo A, Magri S, Mongelli A, Rossi Sebastiano D, Canafoglia L, Grisoli M, Malaguti C, Rivieri F, D'Amico MC, Di Bella D, Franceschetti S, Mariotti C, Taroni F.

J Neurol. 2019 Feb;266(2):378-385. doi: 10.1007/s00415-018-9141-z. Epub 2018 Dec 4.

PMID:
30515630
18.

HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond.

Marini C, Porro A, Rastetter A, Dalle C, Rivolta I, Bauer D, Oegema R, Nava C, Parrini E, Mei D, Mercer C, Dhamija R, Chambers C, Coubes C, Thévenon J, Kuentz P, Julia S, Pasquier L, Dubourg C, Carré W, Rosati A, Melani F, Pisano T, Giardino M, Innes AM, Alembik Y, Scheidecker S, Santos M, Figueiroa S, Garrido C, Fusco C, Frattini D, Spagnoli C, Binda A, Granata T, Ragona F, Freri E, Franceschetti S, Canafoglia L, Castellotti B, Gellera C, Milanesi R, Mancardi MM, Clark DR, Kok F, Helbig KL, Ichikawa S, Sadler L, Neupauerová J, Laššuthova P, Šterbová K, Laridon A, Brilstra E, Koeleman B, Lemke JR, Zara F, Striano P, Soblet J, Smits G, Deconinck N, Barbuti A, DiFrancesco D, LeGuern E, Guerrini R, Santoro B, Hamacher K, Thiel G, Moroni A, DiFrancesco JC, Depienne C.

Brain. 2018 Nov 1;141(11):3160-3178. doi: 10.1093/brain/awy263.

19.

Network characteristics in benign epilepsy with centro-temporal spikes patients indicating defective connectivity during spindle sleep: A partial directed coherence study of EEG signals.

Varotto G, Franceschetti S, Caputo D, Visani E, Canafoglia L, Freri E, Ragona F, Avanzini G, Panzica F.

Clin Neurophysiol. 2018 Nov;129(11):2372-2379. doi: 10.1016/j.clinph.2018.09.008. Epub 2018 Sep 21.

PMID:
30268930
20.

A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability.

Campostrini G, DiFrancesco JC, Castellotti B, Milanesi R, Gnecchi-Ruscone T, Bonzanni M, Bucchi A, Baruscotti M, Ferrarese C, Franceschetti S, Canafoglia L, Ragona F, Freri E, Labate A, Gambardella A, Costa C, Gellera C, Granata T, Barbuti A, DiFrancesco D.

Front Mol Neurosci. 2018 Aug 6;11:269. doi: 10.3389/fnmol.2018.00269. eCollection 2018.

21.

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study.

May P, Girard S, Harrer M, Bobbili DR, Schubert J, Wolking S, Becker F, Lachance-Touchette P, Meloche C, Gravel M, Niturad CE, Knaus J, De Kovel C, Toliat M, Polvi A, Iacomino M, Guerrero-López R, Baulac S, Marini C, Thiele H, Altmüller J, Jabbari K, Ruppert AK, Jurkowski W, Lal D, Rusconi R, Cestèle S, Terragni B, Coombs ID, Reid CA, Striano P, Caglayan H, Siren A, Everett K, Møller RS, Hjalgrim H, Muhle H, Helbig I, Kunz WS, Weber YG, Weckhuysen S, Jonghe P, Sisodiya SM, Nabbout R, Franceschetti S, Coppola A, Vari MS, Kasteleijn-Nolst Trenité D, Baykan B, Ozbek U, Bebek N, Klein KM, Rosenow F, Nguyen DK, Dubeau F, Carmant L, Lortie A, Desbiens R, Clément JF, Cieuta-Walti C, Sills GJ, Auce P, Francis B, Johnson MR, Marson AG, Berghuis B, Sander JW, Avbersek A, McCormack M, Cavalleri GL, Delanty N, Depondt C, Krenn M, Zimprich F, Peter S, Nikanorova M, Kraaij R, van Rooij J, Balling R, Ikram MA, Uitterlinden AG, Avanzini G, Schorge S, Petrou S, Mantegazza M, Sander T, LeGuern E, Serratosa JM, Koeleman BPC, Palotie A, Lehesjoki AE, Nothnagel M, Nürnberg P, Maljevic S, Zara F, Cossette P, Krause R, Lerche H; Epicure Consortium; EuroEPINOMICS CoGIE Consortium; EpiPGX Consortium.

Lancet Neurol. 2018 Aug;17(8):699-708. doi: 10.1016/S1474-4422(18)30215-1. Epub 2018 Jul 17.

22.

Transcutaneous vagal nerve stimulatio (t-VNS): An adjunctive treatment option for refractory epilepsy.

Barbella G, Cocco I, Freri E, Marotta G, Visani E, Franceschetti S, Casazza M.

Seizure. 2018 Aug;60:115-119. doi: 10.1016/j.seizure.2018.06.016. Epub 2018 Jun 18.

23.

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability.

Bonzanni M, DiFrancesco JC, Milanesi R, Campostrini G, Castellotti B, Bucchi A, Baruscotti M, Ferrarese C, Franceschetti S, Canafoglia L, Ragona F, Freri E, Labate A, Gambardella A, Costa C, Rivolta I, Gellera C, Granata T, Barbuti A, DiFrancesco D.

Neurobiol Dis. 2018 Oct;118:55-63. doi: 10.1016/j.nbd.2018.06.012. Epub 2018 Jun 21.

24.

Usefulness of EEG-EMG coherence analysis to confirm epileptic nature of spells mimicking hemifacial spasms.

Ferlazzo E, Gasparini S, Sueri C, Cianci V, Branca D, Franceschetti S, Panzica F, Canafoglia L, Aguglia U.

Clin Neurophysiol. 2018 Aug;129(8):1649-1650. doi: 10.1016/j.clinph.2018.06.001. Epub 2018 Jun 8. No abstract available.

PMID:
29913340
25.

A response to: "Sleep and circadian rhythms in severely brain-injured patients - A comment".

Rossi Sebastiano D, Franceschetti S.

Clin Neurophysiol. 2018 Aug;129(8):1788. doi: 10.1016/j.clinph.2018.04.744. Epub 2018 May 8. No abstract available.

PMID:
29754831
26.

Effect of repetitive transcranial magnetic stimulation on action myoclonus: A pilot study in patients with EPM1.

Rossi Sebastiano D, Magaudda A, Quartarone A, Brizzi T, Visani E, Capovilla G, Beccaria F, Anversa P, Franceschetti S, Canafoglia L.

Epilepsy Behav. 2018 Mar;80:33-36. doi: 10.1016/j.yebeh.2017.11.031. Epub 2018 Feb 3.

PMID:
29396360
27.

Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP2-Dependent K+ Channel Gating.

Ambrosino P, Freri E, Castellotti B, Soldovieri MV, Mosca I, Manocchio L, Gellera C, Canafoglia L, Franceschetti S, Salis B, Iraci N, Miceli F, Ragona F, Granata T, DiFrancesco JC, Taglialatela M.

Mol Neurobiol. 2018 Aug;55(8):7009-7024. doi: 10.1007/s12035-018-0883-5. Epub 2018 Jan 30.

PMID:
29383681
28.

Sleep patterns associated with the severity of impairment in a large cohort of patients with chronic disorders of consciousness.

Rossi Sebastiano D, Visani E, Panzica F, Sattin D, Bersano A, Nigri A, Ferraro S, Parati E, Leonardi M, Franceschetti S.

Clin Neurophysiol. 2018 Mar;129(3):687-693. doi: 10.1016/j.clinph.2017.12.012. Epub 2017 Dec 24.

PMID:
29307451
29.

Corrigendum to "Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study" [Epilepsy Behav 74 (2017) Pages 69-72].

Vasta R, Sarica A, Bisulli F, Di Gennaro G, D'Aniello A, Difrancesco JC, Canafoglia L, Casazza M, Franceschetti S, Stipa C, Tinuper P, Mumoli L, Gambardella A, Labate A.

Epilepsy Behav. 2017 Dec;77:114. doi: 10.1016/j.yebeh.2017.11.011. No abstract available.

PMID:
29173952
30.

Ultrasonography reappraisal of tubal patency in assisted reproduction technology patients: comparison between 2D and 3D-sonohysterosalpingography. A pilot study.

Riganelli L, Casorelli A, Caccetta J, Merlino L, Mariani M, Savone D, Carrone A, Franceschetti S, Aragona C, Pietrangeli D, Aragona A, Capri O, Piccioni MG.

Minerva Ginecol. 2018 Apr;70(2):123-128. doi: 10.23736/S0026-4784.17.04161-2. Epub 2017 Oct 27.

PMID:
29083139
31.

Period3 gene in disorder of consciousness: The role of neuroimaging in understanding the relationship between genotype and sleep. A brief communication.

Bedini G, Bersano A, D'Incerti L, Marotta G, Rosazza C, Rossi Sebastiano D, Franceschetti S, Sattin D, Leonardi M, Nigri A, Ferraro S, Parati EA.

J Neurol Sci. 2017 Oct 15;381:220-225. doi: 10.1016/j.jns.2017.08.3253. Epub 2017 Aug 30.

PMID:
28991686
32.

Variable course of Unverricht-Lundborg disease: Early prognostic factors.

Canafoglia L, Ferlazzo E, Michelucci R, Striano P, Magaudda A, Gambardella A, Pasini E, Belcastro V, Riguzzi P, Fanella M, Granata T, Beccaria F, Trentini C, Bianchi A, Aguglia U, Panzica F, Franceschetti S.

Neurology. 2017 Oct 17;89(16):1691-1697. doi: 10.1212/WNL.0000000000004518. Epub 2017 Sep 20.

PMID:
28931642
33.

Epileptic spikes in Rasmussen's encephalitis: Migratory pattern and short-term evolution. A MEG study.

Rossi Sebastiano D, Visani E, Duran D, Freri E, Panzica F, Chiapparini L, Ragona F, Granata T, Franceschetti S.

Clin Neurophysiol. 2017 Oct;128(10):1898-1905. doi: 10.1016/j.clinph.2017.07.401. Epub 2017 Jul 28.

PMID:
28826020
34.

Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study.

Vasta R, Sarica A, Bisulli F, Di Gennaro G, D'Aniello A, Difrancesco JC, Canafoglia L, Casazza M, Franceschetti S, Stipa C, Tinuper P, Mumoli L, Gambardella A, Labate A.

Epilepsy Behav. 2017 Sep;74:69-72. doi: 10.1016/j.yebeh.2017.06.017. Epub 2017 Jul 17. Erratum in: Epilepsy Behav. 2017 Dec;77:114.

PMID:
28728046
35.

Post-translational dysfunctions in channelopathies of the nervous system.

Terragni B, Scalmani P, Franceschetti S, Cestèle S, Mantegazza M.

Neuropharmacology. 2018 Apr;132:31-42. doi: 10.1016/j.neuropharm.2017.05.028. Epub 2017 May 29. Review.

PMID:
28571716
36.

The impact of genetic and experimental studies on classification and therapy of the epilepsies.

Avanzini G, Mantegazza M, Terragni B, Canafoglia L, Scalmani P, Franceschetti S.

Neurosci Lett. 2018 Feb 22;667:17-26. doi: 10.1016/j.neulet.2017.05.026. Epub 2017 May 15. Review.

PMID:
28522348
37.

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

Oliver KL, Franceschetti S, Milligan CJ, Muona M, Mandelstam SA, Canafoglia L, Boguszewska-Chachulska AM, Korczyn AD, Bisulli F, Di Bonaventura C, Ragona F, Michelucci R, Ben-Zeev B, Straussberg R, Panzica F, Massano J, Friedman D, Crespel A, Engelsen BA, Andermann F, Andermann E, Spodar K, Lasek-Bal A, Riguzzi P, Pasini E, Tinuper P, Licchetta L, Gardella E, Lindenau M, Wulf A, Møller RS, Benninger F, Afawi Z, Rubboli G, Reid CA, Maljevic S, Lerche H, Lehesjoki AE, Petrou S, Berkovic SF.

Ann Neurol. 2017 May;81(5):677-689. doi: 10.1002/ana.24929.

PMID:
28380698
38.

Alternating Hemiplegia and Epilepsia Partialis Continua: A new phenotype for a novel compound TBC1D24 mutation.

Ragona F, Castellotti B, Salis B, Magri S, DiFrancesco JC, Nardocci N, Franceschetti S, Gellera C, Granata T.

Seizure. 2017 Apr;47:71-73. doi: 10.1016/j.seizure.2017.03.003. Epub 2017 Mar 6.

39.

Evidence of altered pressure pain thresholds in persons with disorders of consciousness as measured by the Nociception Coma Scale-Italian version.

Sattin D, Schnakers C, Pagani M, Arenare F, Devalle G, Giunco F, Guizzetti G, Lanfranchi M, Giovannetti AM, Covelli V, Bersano A, Nigri A, Minati L, Rossi Sebastiano D, Parati E, Bruzzone M, Franceschetti S, Leonardi M.

Neuropsychol Rehabil. 2018 Dec;28(8):1295-1310. doi: 10.1080/09602011.2017.1290532. Epub 2017 Feb 28. Erratum in: Neuropsychol Rehabil. 2018 Dec;28(8):x.

PMID:
28278590
40.

Movement-activated cortical myoclonus in Dravet syndrome.

Canafoglia L, Ragona F, Panzica F, Piazza E, Freri E, Binelli S, Scaioli V, Avanzini G, Granata T, Franceschetti S.

Epilepsy Res. 2017 Feb;130:47-52. doi: 10.1016/j.eplepsyres.2017.01.007. Epub 2017 Jan 19.

PMID:
28126647
41.

The network sustaining action myoclonus: a MEG-EMG study in patients with EPM1.

Franceschetti S, Canafoglia L, Rotondi F, Visani E, Granvillano A, Panzica F.

BMC Neurol. 2016 Nov 7;16(1):214.

42.

Primary cutaneous B-cell lymphoma other than marginal zone: clinicopathologic analysis of 161 cases: Comparison with current classification and definition of prognostic markers.

Lucioni M, Berti E, Arcaini L, Croci GA, Maffi A, Klersy C, Goteri G, Tomasini C, Quaglino P, Riboni R, Arra M, Dallera E, Grandi V, Alaibac M, Ramponi A, Rattotti S, Cabras MG, Franceschetti S, Fraternali-Orcioni G, Zerbinati N, Onida F, Ascani S, Fierro MT, Rupoli S, Gambacorta M, Zinzani PL, Pimpinelli N, Santucci M, Paulli M.

Cancer Med. 2016 Oct;5(10):2740-2755. doi: 10.1002/cam4.865. Epub 2016 Sep 26.

43.

Cerebellar Involvement in Patients with Mild to Moderate Myoclonus Due to EPM1: Structural and Functional MRI Findings in Comparison with Healthy Controls and Ataxic Patients.

Nigri A, Visani E, Bertolino N, Nanetti L, Mariotti C, Panzeri M, Bruzzone MG, Franceschetti S, Canafoglia L.

Brain Topogr. 2017 May;30(3):380-389. doi: 10.1007/s10548-016-0534-y. Epub 2016 Oct 26.

PMID:
27785699
44.

PARADISE 24 instrument: An observational study on psychosocial difficulties, quality of life, and disability levels in patients with epilepsy.

Quintas R, Cerniauskaite M, Giovannetti AM, Schiavolin S, Raggi A, Covelli V, Villani F, Didato G, Deleo F, Franceschetti S, Binelli S, Canafoglia L, Casazza M, Leonardi M.

Epilepsy Behav. 2016 Nov;64(Pt A):160-165. doi: 10.1016/j.yebeh.2016.08.019. Epub 2016 Oct 12.

PMID:
27743548
45.

The neural correlates of lexical processing in disorders of consciousness.

Nigri A, Catricalà E, Ferraro S, Bruzzone MG, D'Incerti L, Sattin D, Sebastiano DR, Franceschetti S, Marotta G, Benti R, Leonardi M, Cappa SF; CRC - Coma Research Centre members.

Brain Imaging Behav. 2017 Oct;11(5):1526-1537. doi: 10.1007/s11682-016-9613-7.

PMID:
27738996
46.

Neurophysiology of myoclonus and progressive myoclonus epilepsies.

Avanzini G, Shibasaki H, Rubboli G, Canafoglia L, Panzica F, Franceschetti S, Hallett M.

Epileptic Disord. 2016 Sep 1;18(S2):11-27. Review.

PMID:
27702708
47.

Sialidoses.

Franceschetti S, Canafoglia L.

Epileptic Disord. 2016 Sep 1;18(S2):89-93. Review.

PMID:
27621198
48.

Unverricht-Lundborg disease.

Crespel A, Ferlazzo E, Franceschetti S, Genton P, Gouider R, Kälviäinen R, Korja M, Lehtinen MK, Mervaala E, Simonato M, Vaarmann A.

Epileptic Disord. 2016 Sep 1;18(S2):28-37. Review.

PMID:
27582036
49.

Early effect of dalfampridine in patients with MS: A multi-instrumental approach to better investigate responsiveness.

Brambilla L, Rossi Sebastiano D, Aquino D, Torri Clerici V, Brenna G, Moscatelli M, Frangiamore R, Giovannetti AM, Antozzi C, Mantegazza R, Franceschetti S, Bruzzone MG, Erbetta A, Confalonieri P.

J Neurol Sci. 2016 Sep 15;368:402-7. doi: 10.1016/j.jns.2016.06.019. Epub 2016 Jul 2.

PMID:
27538672
50.

Ovarian function during hormonal contraception assessed by endocrine and sonographic markers: a systematic review.

D'Arpe S, Di Feliciantonio M, Candelieri M, Franceschetti S, Piccioni MG, Bastianelli C.

Reprod Biomed Online. 2016 Oct;33(4):436-448. doi: 10.1016/j.rbmo.2016.07.010. Epub 2016 Aug 4. Review.

PMID:
27527655

Supplemental Content

Loading ...
Support Center