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Items: 1 to 50 of 84

1.

Intellectual efficiency in children and adolescents with spina bifida myelomeningocele and shunted hydrocephalus.

Burro F, Cama A, Lertora V, Veneselli E, Rossetti S, Pezzuti L.

Dev Neuropsychol. 2018;43(3):198-206. doi: 10.1080/87565641.2018.1439035. Epub 2018 Feb 16.

PMID:
29451990
2.

ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases.

Stagnaro M, Pisciotta L, Gherzi M, Di Rocco M, Gurrieri F, Parrini E, Prato G, Veneselli E, De Grandis E.

Eur J Paediatr Neurol. 2018 Mar;22(2):264-271. doi: 10.1016/j.ejpn.2018.01.010. Epub 2018 Jan 31.

PMID:
29396171
3.

Personalized therapy in a GRIN1 mutated girl with intellectual disability and epilepsy.

Papa FT, Mancardi MM, Frullanti E, Fallerini C, Della Chiara V, Zalba-Jadraque L, Baldassarri M, Gamucci A, Mari F, Veneselli E, Renieri A.

Clin Dysmorphol. 2018 Jan;27(1):18-20. doi: 10.1097/MCD.0000000000000205. No abstract available.

PMID:
29194067
4.

One hand, two hands, two people: Prospective sensorimotor control in children with autism.

Ansuini C, Podda J, Battaglia FM, Veneselli E, Becchio C.

Dev Cogn Neurosci. 2018 Jan;29:86-96. doi: 10.1016/j.dcn.2017.02.009. Epub 2017 Mar 2.

5.

Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients.

Pisciotta L, Gherzi M, Stagnaro M, Calevo MG, Giannotta M, Vavassori MR, Veneselli E; I.B.AHC Consortium, De Grandis E.

Brain Dev. 2017 Jun;39(6):521-528. doi: 10.1016/j.braindev.2017.02.001. Epub 2017 Feb 27.

PMID:
28249736
6.

Structural Connectivity Analysis in Children with Segmental Callosal Agenesis.

Severino M, Tortora D, Toselli B, Uccella S, Traverso M, Morana G, Capra V, Veneselli E, Fato MM, Rossi A.

AJNR Am J Neuroradiol. 2017 Mar;38(3):639-647. doi: 10.3174/ajnr.A5043. Epub 2017 Jan 19.

7.

Combined early treatment in hemiplegic attacks related to CACNA1A encephalopathy with brain oedema: Blocking the cascade?

Camia F, Pisciotta L, Morana G, Schiaffino MC, Renna S, Carrera P, Ferrari M, Baglietto MG, Veneselli E, Siri L, Mancardi MM.

Cephalalgia. 2017 Oct;37(12):1202-1206. doi: 10.1177/0333102416668655. Epub 2016 Sep 19.

PMID:
27651281
8.

Blood oxidative stress and metallothionein expression in Rett syndrome: Probing for markers.

Pintaudi M, Veneselli E, Voci A, Vignoli A, Castiglione D, Calevo MG, Grasselli E, Ragazzoni M, Cogliati F, Calzari L, Scornavacca GF, Russo S, Vergani L.

World J Biol Psychiatry. 2016 Apr;17(3):198-209. doi: 10.3109/15622975.2015.1077990. Epub 2015 Oct 15. Erratum in: World J Biol Psychiatry. 2016 Apr;17(3):i.

PMID:
26469135
9.

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.

10.

Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion.

Tassano E, Mirabelli-Badenier M, Veneselli E, Puliti A, Lerone M, Vaccari CM, Morana G, Porta S, Gimelli G, Cuoco C.

Mol Cytogenet. 2015 Apr 28;8:31. doi: 10.1186/s13039-015-0134-7. eCollection 2015.

11.

Antiepileptic drugs in Rett Syndrome.

Pintaudi M, Calevo MG, Vignoli A, Baglietto MG, Hayek Y, Traverso M, Giacomini T, Giordano L, Renieri A, Russo S, Canevini M, Veneselli E.

Eur J Paediatr Neurol. 2015 Jul;19(4):446-52. doi: 10.1016/j.ejpn.2015.02.007. Epub 2015 Mar 5.

PMID:
25814391
12.

Epilepsy in Rett syndrome--lessons from the Rett networked database.

Nissenkorn A, Levy-Drummer RS, Bondi O, Renieri A, Villard L, Mari F, Mencarelli MA, Lo Rizzo C, Meloni I, Pineda M, Armstrong J, Clarke A, Bahi-Buisson N, Mejaski BV, Djuric M, Craiu D, Djukic A, Pini G, Bisgaard AM, Melegh B, Vignoli A, Russo S, Anghelescu C, Veneselli E, Hayek J, Ben-Zeev B.

Epilepsia. 2015 Apr;56(4):569-76. doi: 10.1111/epi.12941. Epub 2015 Mar 19.

13.

Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach?

Mirabelli-Badenier M, Morana G, Bruno C, Di Rocco M, Striano P, De Grandis E, Veneselli E, Rossi A, Biancheri R.

Neuropediatrics. 2015 Apr;46(2):104-9. doi: 10.1055/s-0035-1544185. Epub 2015 Feb 16.

PMID:
25686202
14.

Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism.

Fornarino S, Stagnaro M, Rinelli M, Tiziano D, Mancardi MM, Traverso M, Veneselli E, De Grandis E.

Neurology. 2014 Jun 3;82(22):2037-8. doi: 10.1212/WNL.0000000000000473. Epub 2014 May 2. No abstract available.

PMID:
24793181
15.

Epileptic encephalopathy with continuous spike and wave during sleep associated to periventricular leukomalacia.

De Grandis E, Mancardi MM, Carelli V, Carpaneto M, Morana G, Prato G, Mirabelli-Badenier M, Pinto F, Veneselli E, Baglietto MG.

J Child Neurol. 2014 Nov;29(11):1479-85. doi: 10.1177/0883073813508223. Epub 2013 Nov 28.

PMID:
24293309
16.

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
17.

Chronic inflammatory demyelinating polyneuropathy of childhood: clinical and neuroradiological findings.

Rossi DP, Doria Lamba L, Pistorio A, Pedemonte M, Veneselli E, Rossi A.

Neuroradiology. 2013 Oct;55(10):1233-9. doi: 10.1007/s00234-013-1240-z. Epub 2013 Jul 27.

PMID:
23893072
18.

Are psychobiological markers strongly correlated with allostatic load in population with autism spectrum disorders (ASD)?

Minniti G, Lorini R, Veneselli E, Vergani L, Voci A, Calevo MG, Battaglia FM.

Med Hypotheses. 2013 Apr;80(4):506. doi: 10.1016/j.mehy.2012.12.011. Epub 2013 Jan 16. No abstract available.

PMID:
23332179
19.

Lack of SLC2A1 (glucose transporter 1) mutations in 30 Italian patients with alternating hemiplegia of childhood.

De Grandis E, Stagnaro M, Biancheri R, Giannotta M, Gobbi G, Traverso M, Veneselli E, Zara F.

J Child Neurol. 2013 Jul;28(7):863-6. doi: 10.1177/0883073812452789. Epub 2012 Aug 16.

PMID:
22899793
20.

Anti-glutamic acid decarboxylase limbic encephalitis without epilepsy evolving into dementia with cerebellar ataxia.

Mirabelli-Badenier M, Morana G, Pinto F, Uccelli A, Veneselli E, Battaglia FM, Biancheri R, Baglietto MG, Vincent A, Mancardi MM.

Arch Neurol. 2012 Aug;69(8):1064-6. doi: 10.1001/archneurol.2012.234.

PMID:
22507885
21.

Rett networked database: an integrated clinical and genetic network of Rett syndrome databases.

Grillo E, Villard L, Clarke A, Ben Zeev B, Pineda M, Bahi-Buisson N, Hryniewiecka-Jaworska A, Bienvenu T, Armstrong J, Roche-Martinez A, Mari F, Veneselli E, Russo S, Vignoli A, Pini G, Djuric M, Bisgaard AM, Mejaški Bošnjak V, Polgár N, Cogliati F, Ravn K, Pintaudi M, Melegh B, Craiu D, Djukic A, Renieri A.

Hum Mutat. 2012 Jul;33(7):1031-6. doi: 10.1002/humu.22072. Epub 2012 Apr 13.

22.

Pathophysiological role of inflammatory molecules in paediatric ischaemic brain injury.

Mirabelli-Badenier M, Braunersreuther V, Lenglet S, Galan K, Veneselli E, Viviani GL, Mach F, Montecucco F.

Eur J Clin Invest. 2012 Jul;42(7):784-94. doi: 10.1111/j.1365-2362.2012.02640.x. Epub 2012 Jan 17. Review.

PMID:
22248042
23.

Movement lateralization and bimanual coordination in children with Tourette syndrome.

Avanzino L, Martino D, Bove M, De Grandis E, Tacchino A, Pelosin E, Mirabelli M, Veneselli E, Abbruzzese G.

Mov Disord. 2011 Sep;26(11):2114-8. doi: 10.1002/mds.23839. Epub 2011 Jul 7.

PMID:
21932301
24.

Response to rituximab in 3 children with opsoclonus-myoclonus syndrome resistant to conventional treatments.

Battaglia T, De Grandis E, Mirabelli-Badenier M, Boeri L, Morcaldi G, Barabino P, Intra C, Naselli F, Pistoia V, Veneselli E, Conte M.

Eur J Paediatr Neurol. 2012 Mar;16(2):192-5. doi: 10.1016/j.ejpn.2011.05.013. Epub 2011 Jul 6.

PMID:
21737325
25.

The relationship between group A streptococcal infections and Tourette syndrome: a study on a large service-based cohort.

Martino D, Chiarotti F, Buttiglione M, Cardona F, Creti R, Nardocci N, Orefici G, Veneselli E, Rizzo R; Italian Tourette Syndrome Study Group.

Dev Med Child Neurol. 2011 Oct;53(10):951-7. doi: 10.1111/j.1469-8749.2011.04018.x. Epub 2011 Jun 17.

26.

CC and CXC chemokines are pivotal mediators of cerebral injury in ischaemic stroke.

Mirabelli-Badenier M, Braunersreuther V, Viviani GL, Dallegri F, Quercioli A, Veneselli E, Mach F, Montecucco F.

Thromb Haemost. 2011 Mar;105(3):409-20. doi: 10.1160/TH10-10-0662. Epub 2010 Dec 21. Review.

PMID:
21174009
27.

Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders.

De Grandis E, Serrano M, Pérez-Dueñas B, Ormazábal A, Montero R, Veneselli E, Pineda M, González V, Sanmartí F, Fons C, Sans A, Cormand B, Puelles L, Alonso A, Campistol J, Artuch R, García-Cazorla A.

J Inherit Metab Dis. 2010 Dec;33(6):803-9. doi: 10.1007/s10545-010-9200-9. Epub 2010 Sep 18.

PMID:
20852934
28.

Epilepsy in Rett syndrome: clinical and genetic features.

Pintaudi M, Calevo MG, Vignoli A, Parodi E, Aiello F, Baglietto MG, Hayek Y, Buoni S, Renieri A, Russo S, Cogliati F, Giordano L, Canevini M, Veneselli E.

Epilepsy Behav. 2010 Nov;19(3):296-300. doi: 10.1016/j.yebeh.2010.06.051. Epub 2010 Aug 21.

29.

Cognitive profile in spastic paraplegia with thin corpus callosum and mutations in SPG11.

Siri L, Battaglia FM, Tessa A, Rossi A, Rocco MD, Facchinetti S, Mascaretti M, Santorelli FM, Veneselli E, Biancheri R.

Neuropediatrics. 2010 Feb;41(1):35-8. doi: 10.1055/s-0030-1253352. Epub 2010 Jun 22.

PMID:
20571989
30.

Type 1 diabetes and epilepsy: more than a casual association?

Mancardi MM, Striano P, Giannattasio A, Baglietto MG, Errichiello L, Zara F, Prato G, Minuto N, Veneselli E, Lorini R, D'Annunzio G.

Epilepsia. 2010 Feb;51(2):320-1. doi: 10.1111/j.1528-1167.2009.02380.x. No abstract available.

31.

Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl.

Biancheri R, Pessagno A, Baglietto MG, Irani SR, Rossi A, Giribaldi G, Badenier MM, Vincent A, Veneselli E.

J Pediatr. 2010 Feb;156(2):332-4. doi: 10.1016/j.jpeds.2009.07.057.

PMID:
20105645
32.

Long-term follow-up of neuroblastoma-associated opsoclonus-myoclonus-ataxia syndrome.

De Grandis E, Parodi S, Conte M, Angelini P, Battaglia F, Gandolfo C, Pessagno A, Pistoia V, Mitchell WG, Pike M, Haupt R, Veneselli E.

Neuropediatrics. 2009 Jun;40(3):103-11. doi: 10.1055/s-0029-1237723. Epub 2009 Dec 17.

PMID:
20020394
33.

Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep.

Baglietto MG, Mancardi MM, Giannattasio A, Minuto N, Rossi A, Capovilla G, Veneselli E, Lorini R, d'Annunzio G.

Neurol Sci. 2009 Dec;30(6):509-12. doi: 10.1007/s10072-009-0122-y. Epub 2009 Aug 15.

PMID:
19685202
34.

Neonatal diabetes mellitus due to pancreatic agenesis and pervasive developmental disorder.

Giannattasio A, Pintaudi M, Mancardi MM, Battaglia FM, Veneselli E, Lorini R, d'Annunzio G.

Ital J Pediatr. 2009 Jul 31;35(1):23. doi: 10.1186/1824-7288-35-23.

35.

Short latency evoked somatosensory potentials after stimulation of the median nerve in children: normative data.

Doria-Lamba L, Montaldi L, Grosso P, Veneselli E, Giribaldi G.

J Clin Neurophysiol. 2009 Jun;26(3):176-82. doi: 10.1097/WNP.0b013e3181a76a56.

PMID:
19424081
36.

Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations.

Simonati A, Tessa A, Bernardina BD, Biancheri R, Veneselli E, Tozzi G, Bonsignore M, Grosso S, Piemonte F, Santorelli FM.

Pediatr Neurol. 2009 Apr;40(4):271-6. doi: 10.1016/j.pediatrneurol.2008.10.018.

PMID:
19302939
37.

MR imaging findings in 2 cases of late infantile GM1 gangliosidosis.

De Grandis E, Di Rocco M, Pessagno A, Veneselli E, Rossi A.

AJNR Am J Neuroradiol. 2009 Aug;30(7):1325-7. doi: 10.3174/ajnr.A1508. Epub 2009 Mar 11.

38.

Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes.

Russo S, Marchi M, Cogliati F, Bonati MT, Pintaudi M, Veneselli E, Saletti V, Balestrini M, Ben-Zeev B, Larizza L.

Neurogenetics. 2009 Jul;10(3):241-50. doi: 10.1007/s10048-009-0177-1. Epub 2009 Feb 25.

39.

Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosis.

Aiello C, Terracciano A, Simonati A, Discepoli G, Cannelli N, Claps D, Crow YJ, Bianchi M, Kitzmuller C, Longo D, Tavoni A, Franzoni E, Tessa A, Veneselli E, Boldrini R, Filocamo M, Williams RE, Bertini ES, Biancheri R, Carrozzo R, Mole SE, Santorelli FM.

Hum Mutat. 2009 Mar;30(3):E530-40. doi: 10.1002/humu.20975.

PMID:
19177532
40.

A double-blind, parallel, multicenter comparison of L-acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys.

Torrioli MG, Vernacotola S, Peruzzi L, Tabolacci E, Mila M, Militerni R, Musumeci S, Ramos FJ, Frontera M, Sorge G, Marzullo E, Romeo G, Vallee L, Veneselli E, Cocchi E, Garbarino E, Moscato U, Chiurazzi P, D'Iddio S, Calvani M, Neri G.

Am J Med Genet A. 2008 Apr 1;146A(7):803-12. doi: 10.1002/ajmg.a.32268.

PMID:
18286595
41.

Childhood thalidomide neuropathy: a clinical and neurophysiologic study.

Priolo T, Lamba LD, Giribaldi G, De Negri E, Grosso P, De Grandis E, Veneselli E, Buoncompagni A, Viola S, Alpigiani MG, Gandullia P, Calevo MG.

Pediatr Neurol. 2008 Mar;38(3):196-9. doi: 10.1016/j.pediatrneurol.2007.11.004.

PMID:
18279755
42.

Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy.

Orcesi S, Pessagno A, Biancheri R, La Piana R, Mascaretti M, Rossi A, Rice GI, Crow YJ, Fazzi E, Veneselli E.

Eur J Paediatr Neurol. 2008 Sep;12(5):408-11. Epub 2008 Feb 20.

PMID:
18069026
43.

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
44.

A case of major form familial hyperekplexia: prenatal diagnosis and effective treatment with clonazepam.

Doria Lamba L, Giribaldi G, De Negri E, Follo R, De Grandis E, Pintaudi M, Veneselli E.

J Child Neurol. 2007 Jun;22(6):769-72.

PMID:
17641268
45.

Five-year follow-up of a cognitive-behavioural lifestyle multidisciplinary programme for childhood obesity outpatient treatment.

Vignolo M, Rossi F, Bardazza G, Pistorio A, Parodi A, Spigno S, Torrisi C, Gremmo M, Veneselli E, Aicardi G.

Eur J Clin Nutr. 2008 Sep;62(9):1047-57. Epub 2007 Jun 6.

PMID:
17554247
46.

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.

47.
48.

Metabolic and genetic risk factors for migraine in children.

Bottini F, Celle ME, Calevo MG, Amato S, Minniti G, Montaldi L, Di Pasquale D, Cerone R, Veneselli E, Molinari AC.

Cephalalgia. 2006 Jun;26(6):731-7.

PMID:
16686913
49.

Impairment of the production of delta sleep in anorectic adolescents.

Nobili L, Baglietto MG, Beelke M, De Carli F, Di Comite R, Fiocchi I, Rizzo P, Veneselli E, Savoini M, Zanotto E, Ferrillo F.

Sleep. 2004 Dec 15;27(8):1553-9.

PMID:
15683147
50.

Neuroblastic tumors associated with opsoclonus-myoclonus syndrome: histological, immunohistochemical and molecular features of 15 Italian cases.

Gambini C, Conte M, Bernini G, Angelini P, Pession A, Paolucci P, Donfrancesco A, Veneselli E, Mazzocco K, Tonini GP, Raffaghello L, Dominici C, Morando A, Negri F, Favre A, De Bernardi B, Pistoia V.

Virchows Arch. 2003 Jun;442(6):555-62. Epub 2003 Apr 23.

PMID:
12709798

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