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Items: 1 to 50 of 71

1.

Headache attributed to aeroplane travel: the first multicentric survey in a paediatric population affected by primary headaches.

De Carlo D, Toldo I, Tamborino AM, Bolzonella B, Ledda MG, Margari L, Raieli V, Santucci M, Sciruicchio V, Vecchio A, Zanini S, Sartori S, Gatta M, Verrotti A, Battistella PA.

J Headache Pain. 2018 Nov 14;19(1):108. doi: 10.1186/s10194-018-0939-y.

2.

Mycophenolate mofetil, azathioprine and methotrexate usage in paediatric anti-NMDAR encephalitis: A systematic literature review.

Nosadini M, Mohammad SS, Toldo I, Sartori S, Dale RC.

Eur J Paediatr Neurol. 2019 Jan;23(1):7-18. doi: 10.1016/j.ejpn.2018.09.008. Epub 2018 Sep 27.

PMID:
30318435
3.

Tuberous sclerosis-associated neuropsychiatric disorders: a paediatric cohort study.

Toldo I, Brasson V, Miscioscia M, Pelizza MF, Manara R, Sartori S, Mantegazza G, Vecchi M, Nosadini M, Gatta M.

Dev Med Child Neurol. 2019 Feb;61(2):168-173. doi: 10.1111/dmcn.14055. Epub 2018 Oct 9.

PMID:
30298907
4.

First-ever convulsive seizures in children presenting to the emergency department: risk factors for seizure recurrence and diagnosis of epilepsy.

Sartori S, Nosadini M, Tessarin G, Boniver C, Frigo AC, Toldo I, Bressan S, Da Dalt L.

Dev Med Child Neurol. 2019 Jan;61(1):82-90. doi: 10.1111/dmcn.14015. Epub 2018 Sep 7.

PMID:
30191957
5.

Brain malformations associated to Aldh7a1 gene mutations: Report of a novel homozygous mutation and literature review.

Toldo I, Bonardi CM, Bettella E, Polli R, Talenti G, Burlina A, Sartori S, Murgia A.

Eur J Paediatr Neurol. 2018 Nov;22(6):1042-1053. doi: 10.1016/j.ejpn.2018.06.010. Epub 2018 Jul 3. Review.

PMID:
30005813
6.

Rhinencephalon changes in tuberous sclerosis complex.

Manara R, Brotto D, Bugin S, Pelizza MF, Sartori S, Nosadini M, Azzolini S, Iaconetta G, Parazzini C, Murgia A, Peron A, Canevini P, Labriola F, Vignoli A, Toldo I.

Neuroradiology. 2018 Jun 17. doi: 10.1007/s00234-018-2045-x. [Epub ahead of print]

PMID:
29909560
7.

Genetic and imaging features of cerebellar abnormalities in tuberous sclerosis complex: more insights into their pathogenesis.

Manara R, Bugin S, Pelizza MF, Sartori S, Nosadini M, Labriola F, Canevini P, Vignoli A, Toldo I.

Dev Med Child Neurol. 2018 Jul;60(7):724-725. doi: 10.1111/dmcn.13769. No abstract available.

PMID:
29882962
8.

Obesity and Migraine in Childhood.

Eidlitz Markus T, Toldo I.

Curr Pain Headache Rep. 2018 May 3;22(6):42. doi: 10.1007/s11916-018-0696-2. Review.

PMID:
29725875
9.

Neonatal mitochondrial leukoencephalopathy with brain and spinal involvement and high lactate: expanding the phenotype of ISCA2 gene mutations.

Toldo I, Nosadini M, Boscardin C, Talenti G, Manara R, Lamantea E, Legati A, Ghezzi D, Perilongo G, Sartori S.

Metab Brain Dis. 2018 Jun;33(3):805-812. doi: 10.1007/s11011-017-0181-3. Epub 2018 Jan 23. Review.

PMID:
29359243
10.

Pyridoxine-dependent epilepsies: an observational study on clinical, diagnostic, therapeutic and prognostic features in a pediatric cohort.

Falsaperla R, Vari MS, Toldo I, Murgia A, Sartori S, Vecchi M, Suppiej A, Burlina A, Mastrangelo M, Leuzzi V, Marchiani V, De Liso P, Capovilla G, Striano P, Vitaliti G; Italian Society of Pediatric Neurology (SINP: Società Italiana di Neurologia Pediatrica).

Metab Brain Dis. 2018 Feb;33(1):261-269. doi: 10.1007/s11011-017-0150-x. Epub 2017 Nov 25.

PMID:
29178011
11.

Salivary glands abnormalities in oculo-auriculo-vertebral spectrum.

Brotto D, Manara R, Vio S, Ghiselli S, Cantone E, Mardari R, Toldo I, Stritoni V, Castiglione A, Lovo E, Trevisi P, Bovo R, Martini A.

Clin Oral Investig. 2018 Jan;22(1):395-400. doi: 10.1007/s00784-017-2125-z. Epub 2017 May 22.

PMID:
28534125
12.

Neuroimaging Changes in Menkes Disease, Part 2.

Manara R, Rocco MC, D'agata L, Cusmai R, Freri E, Giordano L, Darra F, Procopio E, Toldo I, Peruzzi C, Vittorini R, Spalice A, Fusco C, Nosadini M, Longo D, Sartori S; Menkes Working Group in the Italian Neuroimaging Network for Rare Diseases.

AJNR Am J Neuroradiol. 2017 Oct;38(10):1858-1865. doi: 10.3174/ajnr.A5192. Epub 2017 May 11. Review.

13.

Herpes simplex virus-induced anti-N-methyl-d-aspartate receptor encephalitis: a systematic literature review with analysis of 43 cases.

Nosadini M, Mohammad SS, Corazza F, Ruga EM, Kothur K, Perilongo G, Frigo AC, Toldo I, Dale RC, Sartori S.

Dev Med Child Neurol. 2017 Aug;59(8):796-805. doi: 10.1111/dmcn.13448. Epub 2017 Apr 25. Review.

14.

Pediatric epilepsy and psychiatric comorbidity: preliminary observational data from a prospective study.

Gatta M, Raffagnato A, Mannarini S, Balottin L, Toldo I, Vecchi M, Boniver C.

Minerva Pediatr. 2018 Dec;70(6):501-512. doi: 10.23736/S0026-4946.17.04753-3. Epub 2017 Apr 20.

PMID:
28425688
15.

Erratum to: Oculo-auriculo-vertebral spectrum: going beyond the first and second pharyngeal arch involvement.

Brotto D, Manara R, Ghiselli S, Lovo E, Mardari R, Toldo I, Castiglione A, Schifano G, Stritoni V, Bovo R, Trevisi P, Martini A.

Neuroradiology. 2017 May;59(5):535. doi: 10.1007/s00234-017-1833-z. No abstract available.

PMID:
28364138
16.

Survey on treatments for primary headaches in 13 specialized juvenile Headache Centers: The first multicenter Italian study.

Toldo I, Rattin M, Perissinotto E, De Carlo D, Bolzonella B, Nosadini M, Rossi LN, Vecchio A, Simonati A, Carotenuto M, Scalas C, Sciruicchio V, Raieli V, Mazzotta G, Tozzi E, Valeriani M, Cianchetti C, Balottin U, Guidetti V, Sartori S, Battistella PA.

Eur J Paediatr Neurol. 2017 May;21(3):507-521. doi: 10.1016/j.ejpn.2016.12.009. Epub 2016 Dec 31.

PMID:
28082014
17.

Alexithymia and psychosocial problems among Italian preadolescents. A latent class analysis approach.

Mannarini S, Balottin L, Toldo I, Gatta M.

Scand J Psychol. 2016 Oct;57(5):473-81. doi: 10.1111/sjop.12300. Epub 2016 Jul 4.

PMID:
27376760
18.

Moyamoya syndrome and 6p chromosome rearrangements: Expanding evidences of a new association.

Toldo I, Po' C, Morao V, Talenti G, Causin F, D'Avella D, Tenconi R, Suppiej A, Sartori S.

Eur J Paediatr Neurol. 2016 Sep;20(5):766-71. doi: 10.1016/j.ejpn.2016.02.008. Epub 2016 Feb 27.

PMID:
27236536
19.

Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD.

Doccini S, Sartori S, Maeser S, Pezzini F, Rossato S, Moro F, Toldo I, Przybylski M, Santorelli FM, Simonati A.

J Neurol. 2016 May;263(5):1029-1032. doi: 10.1007/s00415-016-8111-6. Epub 2016 Apr 12. No abstract available.

PMID:
27072142
20.

Plasma exchange in pediatric anti-NMDAR encephalitis: A systematic review.

Suppiej A, Nosadini M, Zuliani L, Pelizza MF, Toldo I, Bertossi C, Tison T, Zoccarato M, Marson P, Giometto B, Dale RC, Sartori S.

Brain Dev. 2016 Aug;38(7):613-22. doi: 10.1016/j.braindev.2016.01.009. Epub 2016 Feb 28. Review.

PMID:
26926399
21.

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
22.

Baby Jerking: A Teaching Video-Recorded Case of Febrile Myoclonus.

Mercolini F, Scarabel F, Di Leo V, Nosadini M, Toldo I, Sartori S.

Mov Disord Clin Pract. 2015 Jul 14;2(4):429-431. doi: 10.1002/mdc3.12203. eCollection 2015 Dec. No abstract available.

23.

Cranial Nerve Abnormalities in Oculo-Auriculo-Vertebral Spectrum.

Manara R, Brotto D, Ghiselli S, Mardari R, Toldo I, Schifano G, Cantone E, Bovo R, Martini A.

AJNR Am J Neuroradiol. 2015 Jul;36(7):1375-80. doi: 10.3174/ajnr.A4273. Epub 2015 Mar 26.

24.

Paediatric anti-N-methyl-D-aspartate receptor encephalitis: The first Italian multicenter case series.

Sartori S, Nosadini M, Cesaroni E, Falsaperla R, Capovilla G, Beccaria F, Mancardi MM, Santangelo G, Giunta L, Boniver C, Cantalupo G, Cappellari A, Costa P, Dalla Bernardina B, Dilena R, Natali Sora MG, Pelizza MF, Pruna D, Serino D, Vanadia F, Vigevano F, Zamponi N, Zanus C, Toldo I, Suppiej A.

Eur J Paediatr Neurol. 2015 Jul;19(4):453-63. doi: 10.1016/j.ejpn.2015.02.006. Epub 2015 Mar 3.

PMID:
25792293
25.

Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancy.

Bertossi C, Cassina M, Cappellari A, Toldo I, Nosadini M, Rigon C, Suppiej A, Sartori S.

Neuropediatrics. 2015 Feb;46(1):56-64. doi: 10.1055/s-0034-1395345. Epub 2015 Jan 7. Review.

PMID:
25565401
26.

Erratum to: Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Verrotti A, Cusmai R, Laino D, Carotenuto M, Esposito M, Falsaperla R, Margari L, Rizzo R, Savasta S, Grosso S, Striano P, Belcastro V, Franzoni E, Curatolo P, Giordano L, Freri E, Matricardi S, Pruna D, Toldo I, Tozzi E, Lobefalo L, Operto F, Altobelli E, Chiarelli F, Spalice A.

J Neurol. 2015 Jan;262(1):124-5. doi: 10.1007/s00415-014-7579-1. No abstract available.

PMID:
25428530
27.

Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Verrotti A, Cusmai R, Laino D, Carotenuto M, Esposito M, Falsaperla R, Margari L, Rizzo R, Savasta S, Grosso S, Striano P, Belcastro V, Franzoni E, Curatolo P, Giordano L, Freri E, Matricardi S, Pruna D, Toldo I, Tozzi E, Lobefalo L, Operto F, Altobelli E, Chiarelli F, Spalice A.

J Neurol. 2015 Jan;262(1):116-23. doi: 10.1007/s00415-014-7542-1. Epub 2014 Oct 18. Erratum in: J Neurol. 2015 Jan;262(1):124-5. Carotenuto, Marco [added]; Esposito, Maria [added].

PMID:
25326049
28.

Clinical guidelines in pediatric headache: evaluation of quality using the AGREE II instrument.

Parisi P, Vanacore N, Belcastro V, Carotenuto M, Del Giudice E, Mariani R, Papetti L, Pavone P, Savasta S, Striano P, Toldo I, Tozzi E, Verrotti A, Raucci U; “Pediatric Headache Commission” of Società Italiana di Neurologia Pediatrica (SINP).

J Headache Pain. 2014 Sep 1;15:57. doi: 10.1186/1129-2377-15-57.

29.

Children with convulsive epileptic seizures presenting to padua pediatric emergency department: the first retrospective population-based descriptive study in an Italian Health District.

Bergamo S, Parata F, Nosadini M, Boniver C, Toldo I, Suppiej A, Vecchi M, Amigoni A, Da Dalt L, Zanconato S, Perilongo G, Sartori S.

J Child Neurol. 2015 Mar;30(3):289-95. doi: 10.1177/0883073814538670. Epub 2014 Jul 9.

PMID:
25008906
30.

Headache in children with Chiari I malformation.

Toldo I, Tangari M, Mardari R, Perissinotto E, Sartori S, Gatta M, Calderone M, Battistella PA.

Headache. 2014 May;54(5):899-908. doi: 10.1111/head.12341. Epub 2014 Apr 25.

PMID:
24766291
31.

Pacemaker in complicated and refractory breath-holding spells: when to think about it?

Sartori S, Nosadini M, Leoni L, de Palma L, Toldo I, Milanesi O, Cerutti A, Suppiej A.

Brain Dev. 2015 Jan;37(1):2-12. doi: 10.1016/j.braindev.2014.02.004. Epub 2014 Mar 12. Review.

PMID:
24630493
32.

Longitudinal electroencephalographic (EEG) findings in pediatric anti-N-methyl-D-aspartate (anti-NMDA) receptor encephalitis: the Padua experience.

Nosadini M, Boniver C, Zuliani L, de Palma L, Cainelli E, Battistella PA, Toldo I, Suppiej A, Sartori S.

J Child Neurol. 2015 Feb;30(2):238-45. doi: 10.1177/0883073813515947. Epub 2014 Jan 5.

PMID:
24396130
33.

Delayed myelination is not a constant feature of Allan-Herndon-Dudley syndrome: report of a new case and review of the literature.

Azzolini S, Nosadini M, Balzarin M, Sartori S, Suppiej A, Mardari R, Greggio NA, Toldo I.

Brain Dev. 2014 Sep;36(8):716-20. doi: 10.1016/j.braindev.2013.10.009. Epub 2013 Nov 19. Review.

PMID:
24268987
34.

Secondary parenchymal and vascular changes after middle cerebral artery stroke in children.

Manara R, Sartori S, Nosadini M, Baracchini C, Citton V, Toldo I, Simioni P, Gentilomo C, Milanese L, Suppiej A.

Neuroradiology. 2013 Oct;55(10):1259-66. doi: 10.1007/s00234-013-1248-4. Epub 2013 Aug 3.

PMID:
23913014
35.

14q12 duplication including FOXG1: is there a common age-dependent epileptic phenotype?

Bertossi C, Cassina M, De Palma L, Vecchi M, Rossato S, Toldo I, Donà M, Murgia A, Boniver C, Sartori S.

Brain Dev. 2014 May;36(5):402-7. doi: 10.1016/j.braindev.2013.06.008. Epub 2013 Jul 6. Review.

PMID:
23838309
36.

De novo trisomy 20p characterized by array comparative genomic hybridization: report of a novel case and review of the literature.

Bartolini L, Sartori S, Lenzini E, Rigon C, Cainelli E, Agrati C, Toldo I, Donà M, Trevisson E.

Gene. 2013 Jul 25;524(2):368-72. doi: 10.1016/j.gene.2013.04.033. Epub 2013 Apr 21. Review.

PMID:
23612255
37.

Short lasting activity-related headaches with sudden onset in children: a case-based reasoning on classification and diagnosis.

Toldo I, De Carlo D, Mardari R, De Palma L, Gatta M, Bolzonella B, Nosadini M, Bartolini L, Sartori S, Battistella PA.

J Headache Pain. 2013 Jan 25;14:3. doi: 10.1186/1129-2377-14-3.

38.

Intrathecal synthesis of oligoclonal bands in rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome: new evidence supporting immunological pathogenesis.

Sartori S, Priante E, Pettenazzo A, Marson P, Suppiej A, Benini F, Perilongo G, Toldo I.

J Child Neurol. 2014 Mar;29(3):421-5. doi: 10.1177/0883073812469050. Epub 2013 Jan 4.

PMID:
23292759
39.

Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies.

de Palma L, Boniver C, Cassina M, Toldo I, Nosadini M, Clementi M, Sartori S.

Epileptic Disord. 2012 Dec;14(4):414-7. doi: 10.1684/epd.2012.0546.

40.

The pharmacological treatment of migraine in children and adolescents: an overview.

Toldo I, De Carlo D, Bolzonella B, Sartori S, Battistella PA.

Expert Rev Neurother. 2012 Sep;12(9):1133-42. doi: 10.1586/ern.12.104. Review.

PMID:
23039392
41.

Osmophobia as an early marker of migraine: a follow-up study in juvenile patients.

De Carlo D, Toldo I, Dal Zotto L, Perissinotto E, Sartori S, Gatta M, Balottin U, Mazzotta G, Moscato D, Raieli V, Rossi LN, Sangermani R, Soriani S, Termine C, Tozzi E, Vecchio A, Zanchin G, Battistella PA.

Cephalalgia. 2012 Apr;32(5):401-6. doi: 10.1177/0333102412438975. Epub 2012 Mar 9.

PMID:
22407655
42.

Chiari 2 without spinal dysraphism: does it blow a hole in the pathogenesis?

Citton V, Toldo I, Balao L, Pettenazzo A, Emanuelli E, Sartori S, Calderone M, Manara R.

J Child Neurol. 2012 Apr;27(4):536-9. doi: 10.1177/0883073811435239. Epub 2012 Feb 28.

PMID:
22378677
43.

Norovirus gastroenteritis and seizures: an atypical case with neuroradiological abnormalities.

Bartolini L, Mardari R, Toldo I, Calderone M, Battistella PA, Laverda AM, Sartori S.

Neuropediatrics. 2011 Aug;42(4):167-9. doi: 10.1055/s-0031-1286349. Epub 2011 Sep 19.

PMID:
21932182
44.

Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?

Toldo I, Bruson A, Casarin A, Salviati L, Boniver C, Sartori S, Montagna P, Battistella PA, Clementi M.

J Headache Pain. 2011 Aug;12(4):435-41. doi: 10.1007/s10194-011-0359-8. Epub 2011 Jun 29.

45.

The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria.

Marangi G, Ricciardi S, Orteschi D, Lattante S, Murdolo M, Dallapiccola B, Biscione C, Lecce R, Chiurazzi P, Romano C, Greco D, Pettinato R, Sorge G, Pantaleoni C, Alfei E, Toldo I, Magnani C, Bonanni P, Martinez F, Serra G, Battaglia D, Lettori D, Vasco G, Baroncini A, Daolio C, Zollino M.

Am J Med Genet A. 2011 Jul;155A(7):1536-45. doi: 10.1002/ajmg.a.34070. Epub 2011 Jun 10.

PMID:
21671391
46.

Pathogenic role of the X-linked cyclin-dependent kinase-like 5 and aristaless-related homeobox genes in epileptic encephalopathy of unknown etiology with onset in the first year of life.

Sartori S, Polli R, Bettella E, Rossato S, Andreoli W, Vecchi M, Giordano L, Accorsi P, Di Rosa G, Toldo I, Zamponi N, Darra F, Dalla Bernardina B, Perilongo G, Boniver C, Murgia A.

J Child Neurol. 2011 Jun;26(6):683-91. doi: 10.1177/0883073810387827. Epub 2011 Apr 11.

PMID:
21482751
47.

Bilateral perisylvian polymicrogyria with cerebellar dysplasia and ectopic neurohypophysis.

Toldo I, Calderone M, Sartori S, Mardari R, Gatta M, Boniver C, Guerrini R, Battistella PA.

J Child Neurol. 2011 Mar;26(3):361-5. doi: 10.1177/0883073810381447. Epub 2011 Jan 27.

PMID:
21273507
48.

Pre- and postprandial electroencephalography in glucose transporter type 1 deficiency syndrome: an illustrative case to discuss the concept of carbohydrate responsiveness.

Parolin G, Drigo P, Toldo I, Boniver C, Gatta M, Burlina A, Laverda AM, Sartori S.

J Child Neurol. 2011 Jan;26(1):103-8. doi: 10.1177/0883073810376444.

PMID:
21212456
49.

Multimodal neuroimaging in a child with sporadic hemiplegic migraine: a contribution to understanding pathogenesis.

Toldo I, Cecchin D, Sartori S, Calderone M, Mardari R, Cattelan F, Laverda AM, Drigo P, Battistella PA.

Cephalalgia. 2011 Apr;31(6):751-6. doi: 10.1177/0333102410392068. Epub 2010 Dec 20.

PMID:
21172953
50.

Dandy-Walker malformation masking the molar tooth sign: an illustrative case with magnetic resonance imaging follow-up.

Sartori S, Ludwig K, Fortuna M, Marzocchi C, Calderone M, Toldo I, Salviati L, Laverda AM, Tenconi R.

J Child Neurol. 2010 Nov;25(11):1419-22. doi: 10.1177/0883073810370477. Epub 2010 Sep 7.

PMID:
20823032

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