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Items: 1 to 50 of 138

1.

Relapse risk factors in anti-N-methyl-D-aspartate receptor encephalitis.

Nosadini M, Granata T, Matricardi S, Freri E, Ragona F, Papetti L, Suppiej A, Valeriani M, Sartori S; Italian Working Group on Paediatric Anti-N-methyl-D-aspartate Receptor Encephalitis.

Dev Med Child Neurol. 2019 Jun 7. doi: 10.1111/dmcn.14267. [Epub ahead of print]

PMID:
31175679
2.

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 May 18. doi: 10.1111/ane.13130. [Epub ahead of print]

PMID:
31102535
3.

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.

PMID:
30986657
4.

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
5.

When the levee breaks: Effects of flood on offshore water contamination and benthic community in the Mediterranean (Ionian Sea).

Mistri M, Pitacco V, Granata T, Moruzzi L, Munari C.

Mar Pollut Bull. 2019 Mar;140:588-596. doi: 10.1016/j.marpolbul.2019.02.005. Epub 2019 Feb 15.

PMID:
30803680
6.

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.

PMID:
30660924
7.

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 MP, Cappelletti S, Cesaroni E, de Palma L, Costa P, Cusmai R, Giordano L, Ferrari A, Freri E, Fusco L, Granata T, Martino T, Mastrangelo M, Bova SM, Parmeggiani L, Ragona F, Sicca F, Striano P, Specchio LM, 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.

Epilepsia. 2018 Dec;59(12):2260-2271. doi: 10.1111/epi.14600. Epub 2018 Nov 19.

PMID:
30451291
8.

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.

9.

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.

10.

Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications.

Verrotti A, Greco M, Varriale G, Tamborino A, Savasta S, Carotenuto M, Elia M, Operto F, Margari L, Belcastro V, Selicorni A, Freri E, Matricardi S, Granata T, Ragona F, Capovilla G, Spalice A, Coppola G, Striano P.

Acta Neurol Scand. 2018 Dec;138(6):523-530. doi: 10.1111/ane.13006. Epub 2018 Aug 14.

PMID:
30109707
11.

The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders.

Rizzo A, Alfei E, Zibordi F, Saletti V, Zorzi G, Freri E, Estienne M, Girgenti V, D'Arrigo S, Esposito S, Buldrini B, Moroni I, Milani D, Granata T, Ardissone A, Eoli M, Molteni B, Bigoni S, Pantaleoni C, Nardocci N, Sciacca FL.

Am J Med Genet B Neuropsychiatr Genet. 2018 Sep;177(6):557-562. doi: 10.1002/ajmg.b.32649. Epub 2018 Aug 14.

PMID:
30105822
12.

The Movement disorder associated with NMDAR antibody-encephalitis is complex and characteristic: an expert video-rating study.

Varley JA, Webb AJS, Balint B, Fung VSC, Sethi KD, Tijssen MAJ, Lynch T, Mohammad SS, Britton F, Evans M, Hacohen Y, Lin JP, Nardocci N, Granata T, Dale RC, Lim MJ, Bhatia KP, Lang AE, Irani SR.

J Neurol Neurosurg Psychiatry. 2019 Jun;90(6):724-726. doi: 10.1136/jnnp-2018-318584. Epub 2018 Jul 21. No abstract available.

13.

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.

14.

Pediatric NMDAR encephalitis: A single center observation study with a closer look at movement disorders.

Granata T, Matricardi S, Ragona F, Freri E, Zibordi F, Andreetta F, Binelli S, Nardocci N.

Eur J Paediatr Neurol. 2018 Mar;22(2):301-307. doi: 10.1016/j.ejpn.2018.01.012. Epub 2018 Feb 1.

PMID:
29396169
15.

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
16.

Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15).

Matricardi S, Darra F, Spalice A, Basti C, Fontana E, Dalla Bernardina B, Elia M, Giordano L, Accorsi P, Cusmai R, De Liso P, Romeo A, Ragona F, Granata T, Concolino D, Carotenuto M, Pavone P, Pruna D, Striano P, Savasta S, Verrotti A.

Acta Neurol Scand. 2018 Jun;137(6):575-581. doi: 10.1111/ane.12902. Epub 2018 Jan 23.

PMID:
29363096
17.

Toxic inorganic pollutants in foods from agricultural producing areas of Southern Italy: Level and risk assessment.

Salvo A, La Torre GL, Mangano V, Casale KE, Bartolomeo G, Santini A, Granata T, Dugo G.

Ecotoxicol Environ Saf. 2018 Feb;148:114-124. doi: 10.1016/j.ecoenv.2017.10.015. Epub 2017 Nov 6.

PMID:
29035753
18.

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
19.

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
20.

Small plastic debris in sediments from the Central Adriatic Sea: Types, occurrence and distribution.

Mistri M, Infantini V, Scoponi M, Granata T, Moruzzi L, Massara F, De Donati M, Munari C.

Mar Pollut Bull. 2017 Nov 15;124(1):435-440. doi: 10.1016/j.marpolbul.2017.07.063. Epub 2017 Aug 2.

PMID:
28779887
21.

A causality algorithm to guide diagnosis and treatment of catatonia due to autoimmune conditions in children and adolescents.

Ferrafiat V, Raffin M, Freri E, Granata T, Nardocci N, Zibordi F, Bodeau N, Benarous X, Olliac B, Riquin E, Xavier J, Viaux S, Haroche J, Amoura Z, Gerardin P, Cohen D, Consoli A.

Schizophr Res. 2018 Oct;200:68-76. doi: 10.1016/j.schres.2017.06.036. Epub 2017 Jun 26.

PMID:
28659239
22.

Perisylvian, including insular, childhood epilepsy: Presurgical workup and surgical outcome.

Freri E, Matricardi S, Gozzo F, Cossu M, Granata T, Tassi L.

Epilepsia. 2017 Aug;58(8):1360-1369. doi: 10.1111/epi.13816. Epub 2017 Jun 23.

23.

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.

24.

Outcome of childhood-onset epilepsy from adolescence to adulthood: Transition issues.

Nabbout R, Andrade DM, Bahi-Buisson N, Cross H, Desquerre I, Dulac O, Granata T, Hirsch E, Navarro V, Ouss L, Pearl PL, Schmidt D, Thiele E, Camfield PR, Camfield CS.

Epilepsy Behav. 2017 Apr;69:161-169. doi: 10.1016/j.yebeh.2016.11.010. Epub 2017 Feb 28. Review.

PMID:
28256379
25.

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.

Neurology. 2017 Mar 14;88(11):1037-1044. doi: 10.1212/WNL.0000000000003716. Epub 2017 Feb 15.

26.

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
27.

FCD Type II and mTOR pathway: Evidence for different mechanisms involved in the pathogenesis of dysmorphic neurons.

Rossini L, Villani F, Granata T, Tassi L, Tringali G, Cardinale F, Aronica E, Spreafico R, Garbelli R.

Epilepsy Res. 2017 Jan;129:146-156. doi: 10.1016/j.eplepsyres.2016.12.002. Epub 2016 Dec 7.

PMID:
28056425
28.

Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study.

Vecchi M, Barba C, De Carlo D, Stivala M, Guerrini R, Albamonte E, Ranalli D, Battaglia D, Lunardi G, Boniver C, Piccolo B, Pisani F, Cantalupo G, Nieddu G, Casellato S, Cappanera S, Cesaroni E, Zamponi N, Serino D, Fusco L, Iodice A, Palestra F, Giordano L, Freri E, De Giorgi I, Ragona F, Granata T, Fiocchi I, Bova SM, Mastrangelo M, Verrotti A, Matricardi S, Fontana E, Caputo D, Darra F, Dalla Bernardina B, Beccaria F, Capovilla G, Baglietto MP, Gagliardi A, Vignoli A, Canevini MP, Perissinotto E, Francione S.

Epilepsia. 2016 Nov;57(11):1808-1816. doi: 10.1111/epi.13574. Epub 2016 Oct 20.

29.

Rasmussen encephalitis tissue transfer program.

Kruse CA, Pardo CA, Hartman AL, Jallo G, Vining EP, Voros J, Gaillard WD, Liu J, Oluigbo C, Malone S, Bleasel AF, Dexter M, Micati A, Velasco TR, Machado HR, Martino AM, Huang A, Wheatley BM, Grant GA, Granata T, Freri E, Garbelli R, Koh S, Nordli DR, Campos AR, O'Neill B, Handler MH, Chapman KE, Wilfong AA, Curry DJ, Yaun A, Madsen JR, Smyth MD, Mercer D, Bingaman W, Harvey AS, Leventer RJ, Lockhart PJ, Gillies G, Pope K, Giller CA, Park YD, Rojiani AM, Sharma SJ, Jenkins P, Tung S, Huynh MN, Chirwa TW, Cepeda C, Levine MS, Chang JW, Owens GC, Vinters HV, Mathern GW.

Epilepsia. 2016 Jun;57(6):1005-7. doi: 10.1111/epi.13383. No abstract available.

30.

Cognitive and neuropsychological evolution in children with anti-NMDAR encephalitis.

Matricardi S, Patrini M, Freri E, Ragona F, Zibordi F, Andreetta F, Nardocci N, Granata T.

J Neurol. 2016 Apr;263(4):765-71. doi: 10.1007/s00415-016-8056-9. Epub 2016 Feb 17.

PMID:
26886205
31.

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability.

Kasher PR, Schertz KE, Thomas M, Jackson A, Annunziata S, Ballesta-Martinez MJ, Campeau PM, Clayton PE, Eaton JL, Granata T, Guillén-Navarro E, Hernando C, Laverriere CE, Liedén A, Villa-Marcos O, McEntagart M, Nordgren A, Pantaleoni C, Pebrel-Richard C, Sarret C, Sciacca FL, Wright R, Kerr B, Glasgow E, Banka S.

Am J Hum Genet. 2016 Feb 4;98(2):363-72. doi: 10.1016/j.ajhg.2015.12.014. Epub 2016 Jan 28.

32.

Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients.

Lamperti C, Invernizzi F, Solazzi R, Freri E, Carella F, Zeviani M, Zibordi F, Fusco C, Zorzi G, Granata T, Garavaglia B, Nardocci N.

Eur J Paediatr Neurol. 2016 Jan;20(1):152-7. doi: 10.1016/j.ejpn.2015.08.006. Epub 2015 Sep 3.

PMID:
26384010
33.

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.

Jaffer F, Avbersek A, Vavassori R, Fons C, Campistol J, Stagnaro M, De Grandis E, Veneselli E, Rosewich H, Gianotta M, Zucca C, Ragona F, Granata T, Nardocci N, Mikati M, Helseth AR, Boelman C, Minassian BA, Johns S, Garry SI, Scheffer IE, Gourfinkel-An I, Carrilho I, Aylett SE, Parton M, Hanna MG, Houlden H, Neville B, Kurian MA, Novy J, Sander JW, Lambiase PD, Behr ER, Schyns T, Arzimanoglou A, Cross JH, Kaski JP, Sisodiya SM.

Brain. 2015 Oct;138(Pt 10):2859-74. doi: 10.1093/brain/awv243. Epub 2015 Aug 21.

34.

Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations.

Canafoglia L, Gilioli I, Invernizzi F, Sofia V, Fugnanesi V, Morbin M, Chiapparini L, Granata T, Binelli S, Scaioli V, Garavaglia B, Nardocci N, Berkovic SF, Franceschetti S.

Neurology. 2015 Jul 28;85(4):316-24. doi: 10.1212/WNL.0000000000001784. Epub 2015 Jun 26.

35.

Electroencephalographic (EEG) Photoparoxysmal Responses Under 5 Years of Age: Diagnostic Implications and Peculiarities.

Binelli S, Ragona F, Canafoglia L, Freri E, Saletti V, Casazza M, Gilioli I, D'Arrigo S, Visani E, Panzica F, Granata T, Riva D, Franceschetti S.

J Child Neurol. 2015 Nov;30(13):1824-30. doi: 10.1177/0883073815583687. Epub 2015 May 5.

PMID:
25944474
36.

Focal seizure, focal dyskinesia, or both? A complex motor phenomenon reveals anti-NMDAR encephalitis.

Freri E, Matricardi S, Patrini M, Binelli S, Andreetta F, Teutonico F, Nardocci N, Granata T.

Seizure. 2015 Apr;27:16-8. doi: 10.1016/j.seizure.2015.02.005. Epub 2015 Feb 14. No abstract available.

37.

Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature.

Ardissone A, Granata T, Legati A, Diodato D, Melchionda L, Lamantea E, Garavaglia B, Ghezzi D, Moroni I.

JIMD Rep. 2015;22:115-20. doi: 10.1007/8904_2015_419. Epub 2015 Mar 13.

38.

Focal seizures versus epileptic spasms in children with focal cortical dysplasia and epilepsy onset in the first year.

Serino D, Freri E, Ragona F, D'Incerti L, Bernardi B, Di Ciommo V, Granata T, Vigevano F, Fusco L.

Epilepsy Res. 2015 Jan;109:203-9. doi: 10.1016/j.eplepsyres.2014.11.006. Epub 2014 Nov 26.

PMID:
25524860
39.

Transition into adulthood: tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis.

Thiele EA, Granata T, Matricardi S, Chugani HT.

Epilepsia. 2014 Aug;55 Suppl 3:29-33. doi: 10.1111/epi.12722. Review.

40.

Refractory absence epilepsy and glut1 deficiency syndrome: a new case report and literature review.

Ragona F, Matricardi S, Castellotti B, Patrini M, Freri E, Binelli S, Granata T.

Neuropediatrics. 2014 Oct;45(5):328-32. doi: 10.1055/s-0034-1378130. Epub 2014 Jun 3. Review.

PMID:
24892788
41.

VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies.

Diodato D, Melchionda L, Haack TB, Dallabona C, Baruffini E, Donnini C, Granata T, Ragona F, Balestri P, Margollicci M, Lamantea E, Nasca A, Powell CA, Minczuk M, Strom TM, Meitinger T, Prokisch H, Lamperti C, Zeviani M, Ghezzi D.

Hum Mutat. 2014 Aug;35(8):983-9. doi: 10.1002/humu.22590. Epub 2014 Jun 24.

42.

Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patients.

Granata T, Matricardi S, Ragona F, Freri E, Casazza M, Villani F, Deleo F, Tringali G, Gobbi G, Tassi L, Lo Russo G, Marras CE, Specchio N, Vigevano F, Fusco L.

Epilepsy Res. 2014 Aug;108(6):1106-19. doi: 10.1016/j.eplepsyres.2014.03.018. Epub 2014 Apr 8.

PMID:
24815913
43.

Long-term outcome after limited cortical resections in two cases of adult-onset Rasmussen encephalitis.

Villani F, Didato G, Deleo F, Tringali G, Garbelli R, Granata T, Marras CE, Cordella R, Spreafico R.

Epilepsia. 2014 May;55(5):e38-43. doi: 10.1111/epi.12596. Epub 2014 Apr 4.

44.

Inflammatory pathways of seizure disorders.

Marchi N, Granata T, Janigro D.

Trends Neurosci. 2014 Feb;37(2):55-65. doi: 10.1016/j.tins.2013.11.002. Epub 2013 Dec 16. Review.

45.

Overview of presurgical assessment and surgical treatment of epilepsy from the Italian League Against Epilepsy.

Guerrini R, Scerrati M, Rubboli G, Esposito V, Colicchio G, Cossu M, Marras CE, Tassi L, Tinuper P, Paola Canevini M, Quarato P, Giordano F, Granata T, Villani F, Giulioni M, Scarpa P, Barbieri V, Bottini G, Del Sole A, Vatti G, Spreafico R, Lo Russo G; Commission for Epilepsy Surgery of the Italian League Against Epilepsy.

Epilepsia. 2013 Oct;54 Suppl 7:35-48. doi: 10.1111/epi.12308. Review.

46.

Vagus nerve stimulation for drug-resistant Epilepsia Partialis Continua: report of four cases.

De Benedictis A, Freri E, Rizzi M, Franzini A, Ragona F, Specchio N, Rebessi E, Casazza M, Granata T, Marras CE.

Epilepsy Res. 2013 Nov;107(1-2):163-71. doi: 10.1016/j.eplepsyres.2013.07.010. Epub 2013 Sep 8.

PMID:
24074541
47.

An old drug with a new future: bendamustine in multiple myeloma.

Gentile M, Recchia AG, Mazzone C, Vigna E, Martino M, Morabito L, Lucia E, Bossio S, De Stefano L, Granata T, Palummo A, Morabito F.

Expert Opin Pharmacother. 2013 Nov;14(16):2263-80. doi: 10.1517/14656566.2013.837885. Epub 2013 Sep 21. Review.

PMID:
24053161
48.

A role for inflammation in status epilepticus is revealed by a review of current therapeutic approaches.

Janigro D, Iffland PH 2nd, Marchi N, Granata T.

Epilepsia. 2013 Sep;54 Suppl 6:30-2. doi: 10.1111/epi.12271. Review.

49.

Enumeration of interleukin-10-positive B cells from peripheral blood of patients with chronic lymphocytic leukemia.

Rossi M, Gentile M, Toscano R, Recchia AG, Bossio S, Caruso N, De Stefano L, Granata T, Pellicanò M, Vigna E, Tagliaferri P, Tassone P, Morabito F.

Leuk Lymphoma. 2014 Jun;55(6):1394-6. doi: 10.3109/10428194.2013.824078. Epub 2014 Jan 24. No abstract available.

PMID:
23998252
50.

Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndrome.

Verrotti A, Cusmai R, Nicita F, Pizzolorusso A, Elia M, Zamponi N, Cesaroni E, Granata T, De Giorgi I, Giordano L, Grosso S, Pavone P, Franzoni E, Coppola G, Cerminara C, Curatolo P, Savasta S, Striano P, Parisi P, Romeo A, Spalice A.

J Pediatr. 2013 Dec;163(6):1754-8. doi: 10.1016/j.jpeds.2013.07.022. Epub 2013 Aug 27.

PMID:
23992680

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