Zanotta N - Search Results

1

A case of a childhood onset developmental encephalopathy with a novel de novo truncating variant in the Membrane Protein Palmitoylated 5 (MPP5) gene.

Zanotta N, Panzeri E, Minghetti S, Citterio A, Giorda R, Marelli S, Bassi MT, Zucca C. Zanotta N, et al. Seizure. 2024 Mar;116:151-155. doi: 10.1016/j.seizure.2023.01.015. Epub 2023 Jan 23. Seizure. 2024. PMID: 36710240

2

Clinical experience with topiramate dosing and serum levels in patients with epilepsy.

Zanotta N, Raggi ME, Radice L, Degrate A, Bresolin N, Zucca C. Zanotta N, et al. Seizure. 2006 Mar;15(2):86-92. doi: 10.1016/j.seizure.2005.11.003. Epub 2006 Jan 6. Seizure. 2006. PMID: 16406695 Free article.

3

Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.

Zucca C, Redaelli F, Epifanio R, Zanotta N, Romeo A, Lodi M, Veggiotti P, Airoldi G, Panzeri C, Romaniello R, De Polo G, Bonanni P, Cardinali S, Baschirotto C, Martorell L, Borgatti R, Bresolin N, Bassi MT. Zucca C, et al. Among authors: zanotta n. Arch Neurol. 2008 Apr;65(4):489-94. doi: 10.1001/archneur.65.4.489. Arch Neurol. 2008. PMID: 18413471 Free article.

4

A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation.

Romaniello R, Zucca C, Tonelli A, Bonato S, Baschirotto C, Zanotta N, Epifanio R, Righini A, Bresolin N, Bassi MT, Borgatti R. Romaniello R, et al. Among authors: zanotta n. J Neurol Neurosurg Psychiatry. 2010 Aug;81(8):840-3. doi: 10.1136/jnnp.2008.163402. J Neurol Neurosurg Psychiatry. 2010. PMID: 20682717

5

Paroxysmal phenomena in severe disabled children with refractory seizures. From clinical to long-video-EEG processing data to re-examine suspect events.

Arcieri S, Zanotta N, Gnatkovsky V, Avantaggiato P, Formica F, Epifanio R, Angelini L, Strazzer S, Zucca C. Arcieri S, et al. Among authors: zanotta n. Res Dev Disabil. 2015 Jan;36C:125-133. doi: 10.1016/j.ridd.2014.08.040. Epub 2014 Oct 18. Res Dev Disabil. 2015. PMID: 25462473

6

Long-term follow-up of a patient with 5q31.3 microdeletion syndrome and the smallest de novo 5q31.2q31.3 deletion involving PURA.

Bonaglia MC, Zanotta N, Giorda R, D'Angelo G, Zucca C. Bonaglia MC, et al. Among authors: zanotta n. Mol Cytogenet. 2015 Nov 14;8:89. doi: 10.1186/s13039-015-0193-9. eCollection 2015. Mol Cytogenet. 2015. PMID: 26582469 Free PMC article.

7

Late Post-traumatic Epilepsy in Children and Young Adults: Impropriety of Long-Term Antiepileptic Prophylaxis and Risks in Tapering.

Strazzer S, Pozzi M, Avantaggiato P, Zanotta N, Epifanio R, Beretta E, Formica F, Locatelli F, Galbiati S, Clementi E, Zucca C. Strazzer S, et al. Among authors: zanotta n. Paediatr Drugs. 2016 Jun;18(3):235-42. doi: 10.1007/s40272-016-0167-3. Paediatr Drugs. 2016. PMID: 26913859 Free article.

8

Electrical status epilepticus during sleep in Mowat-Wilson syndrome.

Bonanni P, Negrin S, Volzone A, Zanotta N, Epifanio R, Zucca C, Osanni E, Petacchi E, Fabbro F. Bonanni P, et al. Among authors: zanotta n. Brain Dev. 2017 Oct;39(9):727-734. doi: 10.1016/j.braindev.2017.04.013. Epub 2017 May 10. Brain Dev. 2017. PMID: 28501473

9

Partial deletion of DEPDC5 in a child with focal epilepsy.

Bonaglia MC, Giorda R, Epifanio R, Bertuzzo S, Marelli S, Gerard M, Andrieux J, Zanotta N, Zucca C. Bonaglia MC, et al. Among authors: zanotta n. Epilepsia Open. 2016 Aug 25;1(3-4):140-144. doi: 10.1002/epi4.12012. eCollection 2016 Dec. Epilepsia Open. 2016. PMID: 29588938 Free PMC article.

10

Novel epilepsy phenotype associated to a known SCN8A mutation.

Epifanio R, Zanotta N, Giorda R, Bardoni A, Zucca C. Epifanio R, et al. Among authors: zanotta n. Seizure. 2019 Apr;67:15-17. doi: 10.1016/j.seizure.2019.01.017. Epub 2019 Mar 4. Seizure. 2019. PMID: 30851583 Free article. No abstract available.

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