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Items: 1 to 50 of 152

1.

Neurodevelopmental problems of unaccompanied refugee and migrant children: a new challenge for pediatric neurologists.

Fazzi E, Korff C, Bernabe Gelot A, Leroy P, Rivier F, San Antonio-Arce V, Veggiotti P.

Dev Med Child Neurol. 2019 Jun 10. doi: 10.1111/dmcn.14275. [Epub ahead of print] No abstract available.

PMID:
31183863
2.

Food and Food Products on the Italian Market for Ketogenic Dietary Treatment of Neurological Diseases.

Leone A, De Amicis R, Lessa C, Tagliabue A, Trentani C, Ferraris C, Battezzati A, Veggiotti P, Foppiani A, Ravella S, Bertoli S.

Nutrients. 2019 May 17;11(5). pii: E1104. doi: 10.3390/nu11051104. Review.

3.

The spectrum of intermediate SCN8A-related epilepsy.

Johannesen KM, Gardella E, Encinas AC, Lehesjoki AE, Linnankivi T, Petersen MB, Lund ICB, Blichfeldt S, Miranda MJ, Pal DK, Lascelles K, Procopis P, Orsini A, Bonuccelli A, Giacomini T, Helbig I, Fenger CD, Sisodiya SM, Hernandez-Hernandez L, Krithika S, Rumple M, Masnada S, Valente M, Cereda C, Giordano L, Accorsi P, Bürki SE, Mancardi M, Korff C, Guerrini R, von Spiczak S, Hoffman-Zacharska D, Mazurczak T, Coppola A, Buono S, Vecchi M, Hammer MF, Varesio C, Veggiotti P, Lal D, Brünger T, Zara F, Striano P, Rubboli G, Møller RS.

Epilepsia. 2019 May;60(5):830-844. doi: 10.1111/epi.14705. Epub 2019 Apr 10.

PMID:
30968951
4.

Mild phenotype in Molybdenum cofactor deficiency: A new patient and review of the literature.

Scelsa B, Gasperini S, Righini A, Iascone M, Brazzoduro VG, Veggiotti P.

Mol Genet Genomic Med. 2019 Jun;7(6):e657. doi: 10.1002/mgg3.657. Epub 2019 Mar 21.

5.

Dynamic gray matter volume changes in pediatric multiple sclerosis: A 3.5 year MRI study.

De Meo E, Meani A, Moiola L, Ghezzi A, Veggiotti P, Filippi M, Rocca MA.

Neurology. 2019 Apr 9;92(15):e1709-e1723. doi: 10.1212/WNL.0000000000007267. Epub 2019 Mar 13.

PMID:
30867274
6.

Spontaneous MRI improvement and absence of cerebral calcification in Aicardi-Goutières syndrome: Diagnostic and disease-monitoring implications.

Tonduti D, Izzo G, D'Arrigo S, Riva D, Moroni I, Zorzi G, Cavallera V, Pichiecchio A, Uggetti C, Veggiotti P, Orcesi S, Chiapparini L, Parazzini C.

Mol Genet Metab. 2019 Apr;126(4):489-494. doi: 10.1016/j.ymgme.2019.02.006. Epub 2019 Feb 25.

PMID:
30826161
7.

Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome.

De Giorgis V, Masnada S, Varesio C, Chiappedi MA, Zanaboni M, Pasca L, Filippini M, Macasaet JA, Valente M, Ferraris C, Tagliabue A, Veggiotti P.

Brain Behav. 2019 Mar;9(3):e01224. doi: 10.1002/brb3.1224. Epub 2019 Feb 4.

8.

Re-emergence of SSPE: Consequence of the decline of adherence to vaccination programmes?

Masnada S, Zuccotti GV, Bova SM, Gatti H, Morabito V, Santarone ME, Bianchimano B, Dilillo D, Fusco L, Veggiotti P.

Eur J Paediatr Neurol. 2019 Mar;23(2):338-340. doi: 10.1016/j.ejpn.2018.12.010. Epub 2018 Dec 30. No abstract available.

PMID:
30616885
9.

The phenotype of SCN8A developmental and epileptic encephalopathy.

Gardella E, Marini C, Trivisano M, Fitzgerald MP, Alber M, Howell KB, Darra F, Siliquini S, Bölsterli BK, Masnada S, Pichiecchio A, Johannesen KM, Jepsen B, Fontana E, Anibaldi G, Russo S, Cogliati F, Montomoli M, Specchio N, Rubboli G, Veggiotti P, Beniczky S, Wolff M, Helbig I, Vigevano F, Scheffer IE, Guerrini R, Møller RS.

Neurology. 2018 Sep 18;91(12):e1112-e1124. doi: 10.1212/WNL.0000000000006199. Epub 2018 Aug 31.

PMID:
30171078
10.

Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy.

Dilena R, DiFrancesco JC, Soldovieri MV, Giacobbe A, Ambrosino P, Mosca I, Galli MA, Guez S, Fumagalli M, Miceli F, Cattaneo D, Darra F, Gennaro E, Zara F, Striano P, Castellotti B, Gellera C, Varesio C, Veggiotti P, Taglialatela M.

Neurotherapeutics. 2018 Oct;15(4):1112-1126. doi: 10.1007/s13311-018-0657-9.

PMID:
30112700
11.

Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group.

Kossoff EH, Zupec-Kania BA, Auvin S, Ballaban-Gil KR, Christina Bergqvist AG, Blackford R, Buchhalter JR, Caraballo RH, Cross JH, Dahlin MG, Donner EJ, Guzel O, Jehle RS, Klepper J, Kang HC, Lambrechts DA, Liu YMC, Nathan JK, Nordli DR Jr, Pfeifer HH, Rho JM, Scheffer IE, Sharma S, Stafstrom CE, Thiele EA, Turner Z, Vaccarezza MM, van der Louw EJTM, Veggiotti P, Wheless JW, Wirrell EC; Charlie Foundation; Matthew's Friends; Practice Committee of the Child Neurology Society.

Epilepsia Open. 2018 May 21;3(2):175-192. doi: 10.1002/epi4.12225. eCollection 2018 Jun.

12.

Mild ventriculomegaly from fetal consultation to neurodevelopmental assessment: A single center experience and review of the literature.

Scelsa B, Rustico M, Righini A, Parazzini C, Balestriero MA, Introvini P, Spaccini L, Mastrangelo M, Lista G, Zuccotti GV, Veggiotti P.

Eur J Paediatr Neurol. 2018 Nov;22(6):919-928. doi: 10.1016/j.ejpn.2018.04.001. Epub 2018 Apr 12. Review.

PMID:
29709429
13.

Ketogenic diet use in children with intractable epilepsy secondary to malformations of cortical development: A two- centre experience.

Pasca L, Caraballo RH, De Giorgis V, Reyes JG, Macasaet JA, Masnada S, Armeno M, Musicco M, Tagliabue A, Veggiotti P.

Seizure. 2018 Apr;57:34-37. doi: 10.1016/j.seizure.2018.03.005. Epub 2018 Mar 8.

14.

Effects of adjunctive eslicarbazepine acetate on neurocognitive functioning in children with refractory focal-onset seizures.

Jóźwiak S, Veggiotti P, Moreira J, Gama H, Rocha F, Soares-da-Silva P.

Epilepsy Behav. 2018 Apr;81:1-11. doi: 10.1016/j.yebeh.2018.01.029. Epub 2018 Feb 22.

15.

Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.

Masnada S, Hedrich UBS, Gardella E, Schubert J, Kaiwar C, Klee EW, Lanpher BC, Gavrilova RH, Synofzik M, Bast T, Gorman K, King MD, Allen NM, Conroy J, Ben Zeev B, Tzadok M, Korff C, Dubois F, Ramsey K, Narayanan V, Serratosa JM, Giraldez BG, Helbig I, Marsh E, O'Brien M, Bergqvist CA, Binelli A, Porter B, Zaeyen E, Horovitz DD, Wolff M, Marjanovic D, Caglayan HS, Arslan M, Pena SDJ, Sisodiya SM, Balestrini S, Syrbe S, Veggiotti P, Lemke JR, Møller RS, Lerche H, Rubboli G.

Brain. 2017 Sep 1;140(9):2337-2354. doi: 10.1093/brain/awx184.

PMID:
29050392
16.

Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet.

Cappuccio G, Pinelli M, Alagia M, Donti T, Day-Salvatore DL, Veggiotti P, De Giorgis V, Lunghi S, Vari MS, Striano P, Brunetti-Pierri N, Kennedy AD, Elsea SH.

PLoS One. 2017 Sep 29;12(9):e0184022. doi: 10.1371/journal.pone.0184022. eCollection 2017.

17.

MRI substrates of sustained attention system and cognitive impairment in pediatric MS patients.

De Meo E, Moiola L, Ghezzi A, Veggiotti P, Capra R, Amato MP, Pagani E, Fiorino A, Pippolo L, Pera MC, Comi G, Falini A, Filippi M, Rocca MA.

Neurology. 2017 Sep 19;89(12):1265-1273. doi: 10.1212/WNL.0000000000004388. Epub 2017 Aug 18.

18.

Neurobehavioral consequences of continuous spike and waves during slow sleep (CSWS) in a pediatric population: A pattern of developmental hindrance.

De Giorgis V, Filippini M, Macasaet JA, Masnada S, Veggiotti P.

Epilepsy Behav. 2017 Sep;74:1-9. doi: 10.1016/j.yebeh.2017.01.018. Epub 2017 Jun 24.

PMID:
28654799
19.

The face of Glut1-DS patients: A 3D Craniofacial Morphometric Analysis.

Pucciarelli V, Bertoli S, Codari M, De Amicis R, De Giorgis V, Battezzati A, Veggiotti P, Sforza C.

Clin Anat. 2017 Jul;30(5):644-652. doi: 10.1002/ca.22890. Epub 2017 May 22.

20.

Short-term impact of a classical ketogenic diet on gut microbiota in GLUT1 Deficiency Syndrome: A 3-month prospective observational study.

Tagliabue A, Ferraris C, Uggeri F, Trentani C, Bertoli S, de Giorgis V, Veggiotti P, Elli M.

Clin Nutr ESPEN. 2017 Feb;17:33-37. doi: 10.1016/j.clnesp.2016.11.003. Epub 2016 Dec 18.

PMID:
28361745
21.

Brain correlates of spike and wave discharges in GLUT1 deficiency syndrome.

Vaudano AE, Olivotto S, Ruggieri A, Gessaroli G, De Giorgis V, Parmeggiani A, Veggiotti P, Meletti S.

Neuroimage Clin. 2016 Dec 21;13:446-454. doi: 10.1016/j.nicl.2016.12.026. eCollection 2017.

22.

Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.

von Stülpnagel C, Ensslen M, Møller RS, Pal DK, Masnada S, Veggiotti P, Piazza E, Dreesmann M, Hartlieb T, Herberhold T, Hughes E, Koch M, Kutzer C, Hoertnagel K, Nitanda J, Pohl M, Rostásy K, Haack TB, Stöhr K, Kluger G, Borggraefe I.

Eur J Paediatr Neurol. 2017 May;21(3):530-541. doi: 10.1016/j.ejpn.2017.01.001. Epub 2017 Jan 14.

PMID:
28109652
23.

Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy.

Darin N, Reid E, Prunetti L, Samuelsson L, Husain RA, Wilson M, El Yacoubi B, Footitt E, Chong WK, Wilson LC, Prunty H, Pope S, Heales S, Lascelles K, Champion M, Wassmer E, Veggiotti P, de Crécy-Lagard V, Mills PB, Clayton PT.

Am J Hum Genet. 2016 Dec 1;99(6):1325-1337. doi: 10.1016/j.ajhg.2016.10.011.

24.

Facial Evaluation in Holoprosencephaly.

Pucciarelli V, Bertoli S, Codari M, Veggiotti P, Battezzati A, Sforza C.

J Craniofac Surg. 2017 Jan;28(1):e22-e28. doi: 10.1097/SCS.0000000000003171.

PMID:
27875510
25.

The changing face of dietary therapy for epilepsy.

Pasca L, De Giorgis V, Macasaet JA, Trentani C, Tagliabue A, Veggiotti P.

Eur J Pediatr. 2016 Oct;175(10):1267-76. doi: 10.1007/s00431-016-2765-z. Epub 2016 Sep 1. Review.

PMID:
27586246
26.

Atypical Manifestations in Glut1 Deficiency Syndrome.

De Giorgis V, Varesio C, Baldassari C, Piazza E, Olivotto S, Macasaet J, Balottin U, Veggiotti P.

J Child Neurol. 2016 Aug;31(9):1174-80. doi: 10.1177/0883073816650033. Epub 2016 Jun 1.

PMID:
27250207
27.

Extrastriate visual cortex in idiopathic occipital epilepsies: The contribution of retinotopic areas to spike generation.

Meletti S, Ruggieri A, Avanzini P, Caramaschi E, Filippini M, Bergonzini P, Monti G, Vignoli A, Olivotto S, Mastrangelo M, Santucci M, Gobbi G, Veggiotti P, Vaudano AE.

Epilepsia. 2016 Jun;57(6):896-906. doi: 10.1111/epi.13385. Epub 2016 Apr 19.

28.

Intravenous methylprednisolone pulse therapy for children with epileptic encephalopathy.

Pera MC, Randazzo G, Masnada S, Dontin SD, De Giorgis V, Balottin U, Veggiotti P.

Funct Neurol. 2015 Jul-Sep;30(3):173-9.

29.

How to Manage Electrical Status Epilepticus in Sleep.

Veggiotti P, Pera MC, Olivotto S, De Giorgis V.

J Clin Neurophysiol. 2016 Feb;33(1):3-9. doi: 10.1097/WNP.0000000000000235. Review.

PMID:
26840869
30.

Treatment of electrical status epilepticus in sleep: A pooled analysis of 575 cases.

van den Munckhof B, van Dee V, Sagi L, Caraballo RH, Veggiotti P, Liukkonen E, Loddenkemper T, Sánchez Fernández I, Buzatu M, Bulteau C, Braun KP, Jansen FE.

Epilepsia. 2015 Nov;56(11):1738-46. doi: 10.1111/epi.13128. Epub 2015 Sep 4.

31.

Regional hippocampal involvement and cognitive impairment in pediatric multiple sclerosis.

Rocca MA, Morelli ME, Amato MP, Moiola L, Ghezzi A, Veggiotti P, Capra R, Pagani E, Portaccio E, Fiorino A, Pippolo L, Pera MC, Comi G, Falini A, Filippi M.

Mult Scler. 2016 Apr;22(5):628-40. doi: 10.1177/1352458515598569. Epub 2015 Aug 18.

PMID:
26286701
32.

Abnormal cerebellar functional MRI connectivity in patients with paediatric multiple sclerosis.

Cirillo S, Rocca MA, Ghezzi A, Valsasina P, Moiola L, Veggiotti P, Amato MP, Comi G, Falini A, Filippi M.

Mult Scler. 2016 Mar;22(3):292-301. doi: 10.1177/1352458515592191. Epub 2015 Jul 10.

PMID:
26163069
33.

Clinical and genetic analysis of a family with two rare reflex epilepsies.

Kasteleijn-Nolst Trenité DG, Volkers L, Strengman E, Schippers HM, Perquin W, de Haan GJ, Gkountidi AO, van't Slot R, van de Graaf SF, Jocic-Jakubi B, Capovilla G, Covanis A, Parisi P, Veggiotti P, Brinciotti M, Incorpora G, Piccioli M, Cantonetti L, Berkovic SF, Scheffer IE, Brilstra EH, Sonsma AC, Bader AJ, de Kovel CG, Koeleman BP.

Seizure. 2015 Jul;29:90-6. doi: 10.1016/j.seizure.2015.03.020. Epub 2015 Apr 6. Erratum in: Seizure. 2015 Dec;33:104. de Graaf, Stan F [corrected to van de Graaf, Stan F].

34.

Short-term effects of ketogenic diet on anthropometric parameters, body fat distribution, and inflammatory cytokine production in GLUT1 deficiency syndrome.

Bertoli S, Neri IG, Trentani C, Ferraris C, De Amicis R, Battezzati A, Veggiotti P, De Giorgis V, Tagliabue A.

Nutrition. 2015 Jul-Aug;31(7-8):981-7. doi: 10.1016/j.nut.2015.02.017. Epub 2015 Mar 31.

PMID:
26059372
35.

Post-operative benefits of animal-assisted therapy in pediatric surgery: a randomised study.

Calcaterra V, Veggiotti P, Palestrini C, De Giorgis V, Raschetti R, Tumminelli M, Mencherini S, Papotti F, Klersy C, Albertini R, Ostuni S, Pelizzo G.

PLoS One. 2015 Jun 3;10(6):e0125813. doi: 10.1371/journal.pone.0125813. eCollection 2015.

36.

Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1.

Rubboli G, Veggiotti P, Pini A, Berardinelli A, Cantalupo G, Bertini E, Tiziano FD, D'Amico A, Piazza E, Abiusi E, Fiori S, Pasini E, Darra F, Gobbi G, Michelucci R.

Epilepsia. 2015 May;56(5):692-8. doi: 10.1111/epi.12977. Epub 2015 Apr 3.

37.

CHD2 variants are a risk factor for photosensitivity in epilepsy.

Galizia EC, Myers CT, Leu C, de Kovel CG, Afrikanova T, Cordero-Maldonado ML, Martins TG, Jacmin M, Drury S, Krishna Chinthapalli V, Muhle H, Pendziwiat M, Sander T, Ruppert AK, Møller RS, Thiele H, Krause R, Schubert J, Lehesjoki AE, Nürnberg P, Lerche H; EuroEPINOMICS CoGIE Consortium, Palotie A, Coppola A, Striano S, Gaudio LD, Boustred C, Schneider AL, Lench N, Jocic-Jakubi B, Covanis A, Capovilla G, Veggiotti P, Piccioli M, Parisi P, Cantonetti L, Sadleir LG, Mullen SA, Berkovic SF, Stephani U, Helbig I, Crawford AD, Esguerra CV, Kasteleijn-Nolst Trenité DG, Koeleman BP, Mefford HC, Scheffer IE, Sisodiya SM.

Brain. 2015 May;138(Pt 5):1198-207. doi: 10.1093/brain/awv052. Epub 2015 Mar 17.

38.

Sporadic and familial glut1ds Italian patients: A wide clinical variability.

De Giorgis V, Teutonico F, Cereda C, Balottin U, Bianchi M, Giordano L, Olivotto S, Ragona F, Tagliabue A, Zorzi G, Nardocci N, Veggiotti P.

Seizure. 2015 Jan;24:28-32. doi: 10.1016/j.seizure.2014.11.009. Epub 2014 Nov 26.

39.

Cognitive impairment in paediatric multiple sclerosis patients is not related to cortical lesions.

Rocca MA, De Meo E, Amato MP, Copetti M, Moiola L, Ghezzi A, Veggiotti P, Capra R, Fiorino A, Pippolo L, Pera MC, Falini A, Comi G, Filippi M.

Mult Scler. 2015 Jun;21(7):956-9. doi: 10.1177/1352458514557303. Epub 2014 Nov 12.

PMID:
25392332
40.

Remitting Tics and Narcolepsy Overlap Associated with Streptococcal Infection: A Case Report.

Baiardi S, Antelmi E, Filardi M, Pizza F, Vandi S, Veggiotti P, Liguori R, Plazzi G.

Mov Disord Clin Pract. 2014 Oct 23;1(4):374-376. doi: 10.1002/mdc3.12079. eCollection 2014 Dec. No abstract available.

41.

The perceived burden of epilepsy: Impact on the quality of life of children and adolescents and their families.

Cianchetti C, Messina P, Pupillo E, Crichiutti G, Baglietto MG, Veggiotti P, Zamponi N, Casellato S, Margari L, Erba G, Beghi E; TASCA study group.

Seizure. 2015 Jan;24:93-101. doi: 10.1016/j.seizure.2014.09.003. Epub 2014 Sep 16.

42.

Transition for patients with epilepsy due to metabolic and mitochondrial disorders.

Kossoff EH, Veggiotti P, Genton P, Desguerre I.

Epilepsia. 2014 Aug;55 Suppl 3:37-40. doi: 10.1111/epi.12709. Review.

43.

Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform.

Della Mina E, Ciccone R, Brustia F, Bayindir B, Limongelli I, Vetro A, Iascone M, Pezzoli L, Bellazzi R, Perotti G, De Giorgis V, Lunghi S, Coppola G, Orcesi S, Merli P, Savasta S, Veggiotti P, Zuffardi O.

Eur J Hum Genet. 2015 Mar;23(3):354-62. doi: 10.1038/ejhg.2014.92. Epub 2014 May 21.

44.

Long-term effects of a ketogenic diet on body composition and bone mineralization in GLUT-1 deficiency syndrome: a case series.

Bertoli S, Trentani C, Ferraris C, De Giorgis V, Veggiotti P, Tagliabue A.

Nutrition. 2014 Jun;30(6):726-8. doi: 10.1016/j.nut.2014.01.005. Epub 2014 Jan 29.

PMID:
24800673
45.

Long-term follow-up in children with benign convulsions associated with gastroenteritis.

Verrotti A, Moavero R, Vigevano F, Cantonetti L, Guerra A, Spezia E, Tricarico A, Nanni G, Agostinelli S, Chiarelli F, Parisi P, Capovilla G, Beccaria F, Spalice A, Coppola G, Franzoni E, Gentile V, Casellato S, Veggiotti P, Malgesini S, Crichiutti G, Balestri P, Grosso S, Zamponi N, Incorpora G, Savasta S, Costa P, Pruna D, Cusmai R.

Eur J Paediatr Neurol. 2014 Sep;18(5):572-7. doi: 10.1016/j.ejpn.2014.04.006. Epub 2014 Apr 14.

PMID:
24780603
46.

Posterior brain damage and cognitive impairment in pediatric multiple sclerosis.

Rocca MA, Absinta M, Amato MP, Moiola L, Ghezzi A, Veggiotti P, Capra R, Portaccio E, Fiorino A, Pippolo L, Pera MC, Horsfield MA, Falini A, Comi G, Filippi M.

Neurology. 2014 Apr 15;82(15):1314-21. doi: 10.1212/WNL.0000000000000309. Epub 2014 Mar 19.

47.

Dietary Treatments and New Therapeutic Perspective in GLUT1 Deficiency Syndrome.

Veggiotti P, De Giorgis V.

Curr Treat Options Neurol. 2014 May;16(5):291. doi: 10.1007/s11940-014-0291-8.

PMID:
24634059
48.

Intranetwork and internetwork functional connectivity abnormalities in pediatric multiple sclerosis.

Rocca MA, Valsasina P, Absinta M, Moiola L, Ghezzi A, Veggiotti P, Amato MP, Horsfield MA, Falini A, Comi G, Filippi M.

Hum Brain Mapp. 2014 Aug;35(8):4180-92. doi: 10.1002/hbm.22469. Epub 2014 Feb 7.

PMID:
24510680
49.

Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian study.

Zamponi N, Passamonti C, Petrelli C, Veggiotti P, Baldassari C, Verrotti A, Capovilla G, Viri M, Coppola G, Vignoli A.

Pediatr Neurol. 2014 Mar;50(3):228-32. doi: 10.1016/j.pediatrneurol.2013.09.016. Epub 2013 Oct 5.

PMID:
24405698
50.

Acute chorea in a child receiving second dose of human papilloma virus vaccine.

Decio A, Balottin U, De Giorgis V, Veggiotti P.

Pediatr Allergy Immunol. 2014 May;25(3):295-6. doi: 10.1111/pai.12164. Epub 2013 Dec 1. No abstract available.

PMID:
24289225

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