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Items: 1 to 50 of 51

1.

Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome.

Lenci G, Calevo MG, Gaggero R, Prato G, Pisciotta L, De Grandis E, Mancardi MM, Baglietto MG, Vigano' M, Veneselli E.

Brain Dev. 2019 Jun;41(6):522-530. doi: 10.1016/j.braindev.2019.02.004. Epub 2019 Feb 20.

PMID:
30797668
2.

Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication.

Verrotti A, Laino D, Rinaldi VE, Suppiej A, Giordano L, Toldo I, Margari L, Parisi P, Rizzo R, Matricardi S, Cusmai R, Grosso S, Gaggero R, Zamponi N, Pavone P, Capovilla G, Rauchenzauner M, Cerminara C, Di Gennaro G, Esposito M, Striano P, Savasta S, Coppola G, Siliquini S, Operto F, Belcastro V, Ragona F, Marseglia GL, Spalice A.

Eur J Neurol. 2016 Feb;23(2):241-6. doi: 10.1111/ene.12840. Epub 2015 Oct 25.

PMID:
26498733
3.

Early classification of childhood focal idiopathic epilepsies: is it possible at the first seizure?

Gaggero R, Pistorio A, Pignatelli S, Rossi A, Mancardi MM, Baglietto MG, Striano P, Verrotti A.

Eur J Paediatr Neurol. 2014 May;18(3):376-80. doi: 10.1016/j.ejpn.2014.01.011. Epub 2014 Feb 16.

PMID:
24589195
4.

Anti-NMDAR encephalitis misdiagnosed as Hashimoto's encephalopathy.

Mirabelli-Badenier M, Biancheri R, Morana G, Fornarino S, Siri L, Celle ME, Veneselli E, Vincent A, Gaggero R, Mancardi MM.

Eur J Paediatr Neurol. 2014 Jan;18(1):72-4. doi: 10.1016/j.ejpn.2013.07.002. Epub 2013 Aug 15.

PMID:
23953644
5.

Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.

Zara F, Specchio N, Striano P, Robbiano A, Gennaro E, Paravidino R, Vanni N, Beccaria F, Capovilla G, Bianchi A, Caffi L, Cardilli V, Darra F, Bernardina BD, Fusco L, Gaggero R, Giordano L, Guerrini R, Incorpora G, Mastrangelo M, Spaccini L, Laverda AM, Vecchi M, Vanadia F, Veggiotti P, Viri M, Occhi G, Budetta M, Taglialatela M, Coviello DA, Vigevano F, Minetti C.

Epilepsia. 2013 Mar;54(3):425-36. doi: 10.1111/epi.12089. Epub 2013 Jan 29.

6.

Epilepsy associated with supratentorial brain tumors under 3 years of life.

Gaggero R, Consales A, Fazzini F, Mancardi MM, Baglietto MG, Nozza P, Rossi A, Pistorio A, Tumolo M, Cama A, Garrè ML, Striano P.

Epilepsy Res. 2009 Dec;87(2-3):184-9. doi: 10.1016/j.eplepsyres.2009.08.012. Epub 2009 Sep 23.

PMID:
19783404
7.

Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature.

Pintaudi M, Baglietto MG, Gaggero R, Parodi E, Pessagno A, Marchi M, Russo S, Veneselli E.

Epilepsy Behav. 2008 Feb;12(2):326-31. Epub 2007 Dec 11. Review.

PMID:
18063413
8.

An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy.

Striano P, Coppola A, Pezzella M, Ciampa C, Specchio N, Ragona F, Mancardi MM, Gennaro E, Beccaria F, Capovilla G, Rasmini P, Besana D, Coppola GG, Elia M, Granata T, Vecchi M, Vigevano F, Viri M, Gaggero R, Striano S, Zara F.

Neurology. 2007 Jul 17;69(3):250-4.

PMID:
17636062
9.

Severe epilepsy in X-linked creatine transporter defect (CRTR-D).

Mancardi MM, Caruso U, Schiaffino MC, Baglietto MG, Rossi A, Battaglia FM, Salomons GS, Jakobs C, Zara F, Veneselli E, Gaggero R.

Epilepsia. 2007 Jun;48(6):1211-3.

10.

Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

Striano P, Mancardi MM, Biancheri R, Madia F, Gennaro E, Paravidino R, Beccaria F, Capovilla G, Dalla Bernardina B, Darra F, Elia M, Giordano L, Gobbi G, Granata T, Ragona F, Guerrini R, Marini C, Mei D, Longaretti F, Romeo A, Siri L, Specchio N, Vigevano F, Striano S, Tortora F, Rossi A, Minetti C, Dravet C, Gaggero R, Zara F.

Epilepsia. 2007 Jun;48(6):1092-6. Epub 2007 Mar 22.

11.

Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations.

Striano P, Specchio N, Biancheri R, Cannelli N, Simonati A, Cassandrini D, Rossi A, Bruno C, Fusco L, Gaggero R, Vigevano F, Bertini E, Zara F, Santorelli FM, Striano S.

Epilepsy Behav. 2007 Feb;10(1):187-91. Epub 2006 Nov 28.

PMID:
17129765
12.

Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations.

Mancardi MM, Striano P, Gennaro E, Madia F, Paravidino R, Scapolan S, Dalla Bernardina B, Bertini E, Bianchi A, Capovilla G, Darra F, Elia M, Freri E, Gobbi G, Granata T, Guerrini R, Pantaleoni C, Parmeggiani A, Romeo A, Santucci M, Vecchi M, Veggiotti P, Vigevano F, Pistorio A, Gaggero R, Zara F.

Epilepsia. 2006 Oct;47(10):1629-35. Erratum in: Epilepsia. 2007 Feb;48(2):409.

13.

Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy.

Madia F, Striano P, Gennaro E, Malacarne M, Paravidino R, Biancheri R, Budetta M, Cilio MR, Gaggero R, Pierluigi M, Minetti C, Zara F.

Neurology. 2006 Oct 10;67(7):1230-5.

PMID:
17030758
14.

Intractable epilepsy secondary to cyclosporine toxicity in children undergoing allogeneic hematopoietic bone marrow transplantation.

Gaggero R, Haupt R, Paola Fondelli M, De Vescovi R, Marino A, Lanino E, Dallorso S, Faraci M.

J Child Neurol. 2006 Oct;21(10):861-6.

PMID:
17005102
15.

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases.

Striano P, Malacarne M, Cavani S, Pierluigi M, Rinaldi R, Cavaliere ML, Rinaldi MM, De Bernardo C, Coppola A, Pintaudi M, Gaggero R, Grammatico P, Striano S, Dallapiccola B, Zara F, Faravelli F.

Am J Med Genet A. 2006 Sep 15;140(18):1944-9.

PMID:
16906558
16.

Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.

Striano P, Lispi ML, Gennaro E, Madia F, Traverso M, Bordo L, Aridon P, Martinelli Boneschi F, Barone B, dalla Bernardina B, Bianchi A, Capovilla G, De Marco P, Dulac O, Gaggero R, Gambardella A, Nabbout R, Prud'homme JF, Day R, Vanadia F, Vecchi M, Veggiotti P, Vigevano F, Viri M, Minetti C, Zara F.

Epilepsia. 2006 Jun;47(6):1029-34.

17.

6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.

Elia M, Striano P, Fichera M, Gaggero R, Castiglia L, Galesi O, Malacarne M, Pierluigi M, Amato C, Musumeci SA, Romano C, Majore S, Grammatico P, Zara F, Striano S, Faravelli F.

Epilepsia. 2006 May;47(5):830-8.

18.

Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the Mediterranean.

Cannelli N, Cassandrini D, Bertini E, Striano P, Fusco L, Gaggero R, Specchio N, Biancheri R, Vigevano F, Bruno C, Simonati A, Zara F, Santorelli FM.

Neurogenetics. 2006 May;7(2):111-7. Epub 2006 Mar 29.

PMID:
16570191
19.

Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy.

Gennaro E, Santorelli FM, Bertini E, Buti D, Gaggero R, Gobbi G, Lini M, Granata T, Freri E, Parmeggiani A, Striano P, Veggiotti P, Cardinali S, Bricarelli FD, Minetti C, Zara F.

Biochem Biophys Res Commun. 2006 Mar 10;341(2):489-93. Epub 2006 Jan 13.

PMID:
16430863
20.

Hashimoto's encephalopathy with selective involvement of the nucleus accumbens: a case report.

Mancardi MM, Fazzini F, Rossi A, Gaggero R.

Neuropediatrics. 2005 Jun;36(3):218-20.

PMID:
15944910
21.

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.

Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, Capovilla G, Chiron C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallée L, Dagna Bricarelli F, Bianchi A, Zara F.

Neurology. 2003 Jun 24;60(12):1961-7.

PMID:
12821740
22.

Mesial temporal sclerosis--a late complication in four allogeneic pediatric recipients with persistent seizures after an acute episode of cyclosporine-A neurotoxicity.

Faraci M, Lanino E, Dallorso S, Morreale G, Cappelli B, Gaggero R, Dini G, Haupt R, Fondelli MP.

Bone Marrow Transplant. 2003 May;31(10):919-22.

PMID:
12748669
23.

No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy.

Madia F, Gennaro E, Cecconi M, Buti D, Capovilla G, Dalla Bernardina B, Elia M, Ferrari A, Fontana E, Gaggero R, Giannotta M, Giordano L, Granata T, La Selva L, Luisa Lispi M, Santucci M, Vanadia F, Veggiotti P, Vigliano P, Viri M, Dagna Bricarelli F, Bianchi A, Zara F.

Epilepsy Res. 2003 Mar;53(3):196-200.

PMID:
12694927
24.

Severe neurologic complications after hematopoietic stem cell transplantation in children.

Faraci M, Lanino E, Dini G, Fondelli MP, Morreale G, Dallorso S, Manzitti C, Calevo MG, Gaggero R, Castagnola E, Haupt R.

Neurology. 2002 Dec 24;59(12):1895-904. Erratum in: Neurology. 2003 Mar 25;60(6):1055.

PMID:
12499480
25.

An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage disease.

Biancheri R, Verbeek E, Rossi A, Gaggero R, Roccatagliata L, Gatti R, van Diggelen O, Verheijen FW, Mancini GM.

Clin Genet. 2002 Jun;61(6):443-7.

PMID:
12121352
26.

Lack of SCN1A mutations in familial febrile seizures.

Malacarne M, Madia F, Gennaro E, Vacca D, Güney AI, Buono S, Bernardina BD, Gaggero R, Gobbi G, Lispi ML, Malamaci D, Melideo G, Roccella M, Sferro C, Tiberti A, Vanadia F, Vigevano F, Viri F, Vitali MR, Bricarelli FD, Bianchi A, Zara F.

Epilepsia. 2002 May;43(5):559-62.

27.

Benign parasomnias and nocturnal frontal epilepsy: differential diagnosis in a case report.

Gaggero R, Devescovi R, Nobili L, Baglietto MG, Zucconi M, Schinardi A.

J Child Neurol. 2001 Aug;16(8):628-31.

PMID:
11510944
28.

Malignant migrating partial seizures in infancy.

Veneselli E, Perrone MV, Di Rocco M, Gaggero R, Biancheri R.

Epilepsy Res. 2001 Jul;46(1):27-32.

PMID:
11395285
29.

Distribution of epileptiform discharges during nREM sleep in the CSWSS syndrome: relationship with sigma and delta activities.

Nobili L, Baglietto MG, Beelke M, De Carli F, De Negri E, Gaggero R, Rosadini G, Veneselli E, Ferrillo F.

Epilepsy Res. 2001 May;44(2-3):119-28.

PMID:
11325568
30.

Epilepsy associated with infantile hemiparesis: predictors of long-term evolution.

Gaggero R, Devescovi R, Zaccone A, Ravera G.

Brain Dev. 2001 Mar;23(1):12-7.

PMID:
11226723
31.

Benzodiazepine (BDZ) treatment of benign childhood epilepsy with centrotemporal spikes (BECCT)

De Negri M, Baglietto MG, Gaggero R.

Brain Dev. 1997 Nov;19(7):506. No abstract available.

PMID:
9408602
32.

Early-onset progressive encephalopathy with migrant, continuous myoclonus.

Gaggero R, Baglietto MP, Curia R, De Negri M.

Childs Nerv Syst. 1996 May;12(5):254-61.

PMID:
8737801
33.

Occlusion of unilateral carotid artery in Down syndrome.

Gaggero R, Donati PT, Curia R, De Negri M.

Brain Dev. 1996 Jan-Feb;18(1):81-3.

PMID:
8907351
34.

Treatment of electrical status epilepticus by short diazepam (DZP) cycles after DZP rectal bolus test.

De Negri M, Baglietto MG, Battaglia FM, Gaggero R, Pessagno A, Recanati L.

Brain Dev. 1995 Sep-Oct;17(5):330-3.

PMID:
8579219
35.

SPECT and epilepsy with continuous spike waves during slow-wave sleep.

Gaggero R, Caputo M, Fiorio P, Pessagno A, Baglietto MG, Muttini P, De Negri M.

Childs Nerv Syst. 1995 Mar;11(3):154-60.

PMID:
7773975
36.

Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome.

Curatolo P, Cilio MR, Del Giudice E, Romano A, Gaggero R, Pessagno A.

Neuropediatrics. 1993 Apr;24(2):77-82.

PMID:
8327066
37.

[The clinical use of dynamic EEG in childhood].

Baglietto MG, Gaggero R, Leoni P.

Minerva Pediatr. 1992 Mar;44(3):65-71. Italian.

PMID:
1518495
38.

[Epilepsy with laughing seizures, hypothalamic hamartoma and precocious puberty. Contributions of MRI, computed EEG topography (CET) and ambulatory EEG (A-EEG)].

Gaggero R, Baglietto MP, Boragno F, Oddone M, Tomà P, De Negri M.

Minerva Pediatr. 1991 Dec;43(12):801-10. Italian.

PMID:
1798407
39.

[Epilepsy and neuropsychological functions].

Gaggero R, Cirrincione M, Baglietto MP.

Minerva Pediatr. 1991 Mar;43(3):237-9. Italian. No abstract available.

PMID:
1870524
40.

Rapid diazepam introduction (venous or rectal) in childhood epilepsy: taxonomic and therapeutic considerations.

De Negri M, Gaggero R, Veneselli E, Pessagno A, Baglietto MG, Pallecchi A.

Brain Dev. 1991;13(1):21-6.

PMID:
2063993
41.

[Neurogenic hypernatremia syndrome in children].

Gaggero R, Pesce F, Barcella L, Boragno F, Corea D, Veneselli E, de Negri M.

Minerva Pediatr. 1991 Jan-Feb;43(1-2):39-43. Italian.

PMID:
2034194
42.

CSF anomalies in children affected by Epilepsia Partialis Continua (EPC).

Gaggero R, Ferraris PC, De Negri M.

Neuropediatrics. 1990 Aug;21(3):143-5.

PMID:
2122270
43.

Computed EEG topography (CET) and childhood epilepsy: two years experience.

De Negri M, Gaggero R, Baglietto MG.

Brain Dev. 1990;12(2):253-6.

PMID:
2193552
44.

Secondary generalized epilepsy in childhood: EEG patterns and correlation with responsiveness to benzodiazepines or ACTH (preliminary note).

De Negri M, Cremonte M, Veneselli E, Gaggero R, Zanotto E, Sannita U, Molinari A.

Brain Dev. 1988;10(6):375-81.

PMID:
2851271
45.

[Neuropsychiatric side effect of anticonvulsants in the child].

De Negri M, Doria L, Gaggero R, Rolando S.

Neuropsychiatr Enfance Adolesc. 1983 Nov-Dec;31(11-12):551-6. Review. French. No abstract available.

PMID:
6424046
46.

[Prognosis of febrile convulsions according to age of onset and response to preventive treatment].

Gaggero R, De Negri M.

Neuropsychiatr Enfance Adolesc. 1983 Nov-Dec;31(11-12):545-50. French. No abstract available.

PMID:
6424045
47.

[A few remarks on the use of anticonvulsant drugs and the value of pharmacokinetic studies in the child].

Gaggero R, De Negri M.

Neuropsychiatr Enfance Adolesc. 1983 Nov-Dec;31(11-12):537-44. French. No abstract available.

PMID:
6424044
48.

[Evolution of childhood epilepsy and its prognosis in adolescence].

De Negri M, Doria L, Gaggero R, Rolando S.

Neuropsychiatr Enfance Adolesc. 1983 Nov-Dec;31(11-12):507-14. French. No abstract available.

PMID:
6424043
49.

[Neurological and psychic side effects of antiepileptic drugs in pediatric age (author's transl)].

De Negri M, Doria L, Gaggero R, Rolando S.

Pediatr Med Chir. 1981 Mar-Jun;3(2-3):159-64. Italian.

PMID:
7343909
50.

[Prognosis of febrile seizures correlated wih age of onset and therapeutic response (author's transl)].

Gaggero R, De Negri M.

Pediatr Med Chir. 1981 Mar-Jun;3(2-3):147-50. Italian. No abstract available.

PMID:
7343908

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