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Items: 1 to 20 of 210

1.

Value of Multimodal Imaging Approach to Diagnosis of Neurosarcoidosis.

Sammarra I, Barbagallo G, Labate A, Mondello B, Albonico G, Maisano M, Cascini GL, Quattrone A, Gambardella A.

Brain Sci. 2019 Sep 21;9(10). pii: E243. doi: 10.3390/brainsci9100243.

2.

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
3.

Declining malformation rates with changed antiepileptic drug prescribing: An observational study.

Tomson T, Battino D, Bonizzoni E, Craig J, Lindhout D, Perucca E, Sabers A, Thomas SV, Vajda F; EURAP Study Group.

Neurology. 2019 Aug 27;93(9):e831-e840. doi: 10.1212/WNL.0000000000008001. Epub 2019 Aug 7.

PMID:
31391249
4.

Usefulness of cardiac parasympathetic index in CPAP-treated patients with obstructive sleep apnea: A preliminary study.

Salsone M, Marelli S, Vescio B, Quattrone A, Gambardella A, Castelnuovo A, Quattrone A, Ferini Strambi L.

J Sleep Res. 2019 Jul 31:e12893. doi: 10.1111/jsr.12893. [Epub ahead of print]

PMID:
31368146
5.

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; Epi25 Collaborative.

Am J Hum Genet. 2019 Aug 1;105(2):267-282. doi: 10.1016/j.ajhg.2019.05.020. Epub 2019 Jul 18.

PMID:
31327507
6.

Functional activity changes in memory and emotional systems of healthy subjects with déjà vu.

Nigro S, Cavalli SM, Cerasa A, Riccelli R, Fortunato F, Bianco MG, Martino I, Chiriaco C, Vaccaro MG, Quattrone A, Gambardella A, Labate A.

Epilepsy Behav. 2019 Aug;97:8-14. doi: 10.1016/j.yebeh.2019.05.018. Epub 2019 Jun 7.

PMID:
31181431
7.

REM-Sleep Behavior Disorder in Patients With Essential Tremor: What Is Its Clinical Significance?

Salsone M, Arabia G, Manfredini L, Quattrone A, Chiriaco C, Vescio B, Sturniolo M, Morelli M, Nistico' R, Novellino F, Gambardella A, Quattrone A.

Front Neurol. 2019 Apr 24;10:315. doi: 10.3389/fneur.2019.00315. eCollection 2019.

8.

Hypertension, seizures, and epilepsy: a review on pathophysiology and management.

Gasparini S, Ferlazzo E, Sueri C, Cianci V, Ascoli M, Cavalli SM, Beghi E, Belcastro V, Bianchi A, Benna P, Cantello R, Consoli D, De Falco FA, Di Gennaro G, Gambardella A, Gigli GL, Iudice A, Labate A, Michelucci R, Paciaroni M, Palumbo P, Primavera A, Sartucci F, Striano P, Villani F, Russo E, De Sarro G, Aguglia U; Epilepsy Study Group of the Italian Neurological Society.

Neurol Sci. 2019 Sep;40(9):1775-1783. doi: 10.1007/s10072-019-03913-4. Epub 2019 May 4. Review.

PMID:
31055731
9.

Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy.

Lerche H, Berkovic SF, Lowenstein DH; EuroEPINOMICS-CoGIE Consortium; EpiPGX Consortium; Epi4K Consortium/Epilepsy Phenome/Genome Project.

N Engl J Med. 2019 Apr 18;380(16):e24. doi: 10.1056/NEJMc1805100. No abstract available.

PMID:
30995385
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.

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

Pippucci T, Licchetta L, Baldassari S, Marconi C, De Luise M, Myers C, Nardi E, Provini F, Cameli C, Minardi R, Bacchelli E, Giordano L, Crichiutti G, d'Orsi G, Seri M, Gasparre G, Mefford HC, Tinuper P, Bisulli F; Collaborative Group of Italian League Against Epilepsy (LICE) Genetic Commission.

Ann Clin Transl Neurol. 2019 Feb 25;6(3):475-485. doi: 10.1002/acn3.722. eCollection 2019 Mar.

12.

A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.

Berghuis B, Stapleton C, Sonsma ACM, Hulst J, de Haan GJ, Lindhout D, Demurtas R; EpiPGX Consortium, Krause R, Depondt C, Kunz WS, Zara F, Striano P, Craig J, Auce P, Marson AG, Stefansson H, O'Brien TJ, Johnson MR, Sills GJ, Wolking S, Lerche H, Sisodiya SM, Sander JW, Cavalleri GL, Koeleman BPC, McCormack M.

Epilepsia Open. 2019 Jan 17;4(1):102-109. doi: 10.1002/epi4.12297. eCollection 2019 Mar.

13.

Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study.

Nabbout R, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, Dahlin M, D Amato L, d'Augères GB, de Vries PJ, Ferreira JC, Feucht M, Fladrowski C, Hertzberg C, Jozwiak S, Lawson JA, Macaya A, Marques R, O'Callaghan F, Qin J, Sander V, Sauter M, Shah S, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Jansen A, Kingswood JC; TOSCA Consortium and TOSCA Investigators.

Epilepsia Open. 2018 Dec 21;4(1):73-84. doi: 10.1002/epi4.12286. eCollection 2019 Mar.

14.

Abdominal Fat SIRT6 Expression and Its Relationship with Inflammatory and Metabolic Pathways in Pre-Diabetic Overweight Patients.

D'Onofrio N, Pieretti G, Ciccarelli F, Gambardella A, Passariello N, Rizzo MR, Barbieri M, Marfella R, Nicoletti G, Balestrieri ML, Sardu C.

Int J Mol Sci. 2019 Mar 6;20(5). pii: E1153. doi: 10.3390/ijms20051153.

15.

Psychiatric Assessment in Patients with Mild Temporal Lobe Epilepsy.

Bruni A, Martino I, Caligiuri ME, Vaccaro MG, Trimboli M, Segura Garcia C, De Fazio P, Gambardella A, Labate A.

Behav Neurol. 2019 Jan 14;2019:4139404. doi: 10.1155/2019/4139404. eCollection 2019.

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.

Synovial sarcoma diagnosis on fine needle cytology sample confirmed by fluorescence in situ hybridisation.

Ronchi A, Panarese I, Aquino G, Gambardella A, Franco R, Cozzolino I.

Cytopathology. 2019 May;30(3):314-317. doi: 10.1111/cyt.12651. Epub 2018 Dec 6. No abstract available.

PMID:
30417957
18.

Potential Role of miRNAs as Theranostic Biomarkers of Epilepsy.

Cava C, Manna I, Gambardella A, Bertoli G, Castiglioni I.

Mol Ther Nucleic Acids. 2018 Dec 7;13:275-290. doi: 10.1016/j.omtn.2018.09.008. Epub 2018 Sep 13. Review.

19.

The application of artificial intelligence to understand the pathophysiological basis of psychogenic nonepileptic seizures.

Vasta R, Cerasa A, Sarica A, Bartolini E, Martino I, Mari F, Metitieri T, Quattrone A, Gambardella A, Guerrini R, Labate A.

Epilepsy Behav. 2018 Oct;87:167-172. doi: 10.1016/j.yebeh.2018.09.008. Epub 2018 Sep 28.

20.

Correction: The landscape of epilepsy-related GATOR1 variants.

Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, 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, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks EH, Jansen FE, Braun K, de Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, NordliJr DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, 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 CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S.

Genet Med. 2019 Aug;21(8):1896. doi: 10.1038/s41436-018-0325-9.

PMID:
30262923

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