Zucca C - Search Results

1

A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical pattern.

Romaniello R, Zucca C, Tenderini E, Arrigoni F, Ragona F, Zorzi G, Bassi MT, Borgatti R. Romaniello R, et al. Among authors: zucca c. J Child Neurol. 2014 Feb;29(2):249-53. doi: 10.1177/0883073813506936. Epub 2013 Oct 29. J Child Neurol. 2014. PMID: 24170257

2

Bilateral perisylvian polymicrogyria in three generations.

Borgatti R, Triulzi F, Zucca C, Piccinelli P, Balottin U, Carrozzo R, Guerrini R. Borgatti R, et al. Among authors: zucca c. Neurology. 1999 Jun 10;52(9):1910-3. doi: 10.1212/wnl.52.9.1910. Neurology. 1999. PMID: 10371547

3

Unilateral periventricular nodular heterotopia associated with diffuse areas of cerebral functional abnormalities.

Borgatti R, Zucca C, Piccinelli P, Macchi HF, Radice L, Tofani A, Benti R, Triulzi F. Borgatti R, et al. Among authors: zucca c. J Child Neurol. 2000 Sep;15(9):622-6. doi: 10.1177/088307380001500910. J Child Neurol. 2000. PMID: 11019794

4

Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment.

Zucca C, Binda S, Borgatti R, Triulzi F, Radice L, Buttè C, Barkhaus PE, Barbi M. Zucca C, et al. Neurology. 2003 Sep 9;61(5):710-2. doi: 10.1212/wnl.61.5.710. Neurology. 2003. PMID: 12963772

5

A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.

Borgatti R, Zucca C, Cavallini A, Ferrario M, Panzeri C, Castaldo P, Soldovieri MV, Baschirotto C, Bresolin N, Dalla Bernardina B, Taglialatela M, Bassi MT. Borgatti R, et al. Among authors: zucca c. Neurology. 2004 Jul 13;63(1):57-65. doi: 10.1212/01.wnl.0000132979.08394.6d. Neurology. 2004. PMID: 15249611

6

Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance Test.

Borgatti R, Piccinelli P, Montirosso R, Donati G, Rampani A, Molteni L, Tofani A, Nicoli F, Zucca C, Bresolin N, Balottin U. Borgatti R, et al. Among authors: zucca c. J Child Neurol. 2004 Jul;19(7):509-15. doi: 10.1177/08830738040190070601. J Child Neurol. 2004. PMID: 15526955

7

Inter-rater reliability of the EEG reading in patients with childhood idiopathic epilepsy.

Piccinelli P, Viri M, Zucca C, Borgatti R, Romeo A, Giordano L, Balottin U, Beghi E. Piccinelli P, et al. Among authors: zucca c. Epilepsy Res. 2005 Aug-Sep;66(1-3):195-8. doi: 10.1016/j.eplepsyres.2005.07.004. Epilepsy Res. 2005. PMID: 16118044

8

Epilepsy and neuropsychologic deficit in a child with cerebellar astrocytoma.

Strazzer S, Zucca C, Fiocchi I, Genitori L, Castelli E. Strazzer S, et al. Among authors: zucca c. J Child Neurol. 2006 Sep;21(9):817-20. doi: 10.1177/08830738060210091701. J Child Neurol. 2006. PMID: 16970895

9

Subtelomeric trisomy 21q: a new benign chromosomal variant.

Bonaglia MC, Marelli S, Gottardi G, Zucca C, Pramparo T, Giorda R, Grasso R, Borgatti R, Zuffardi O. Bonaglia MC, et al. Among authors: zucca c. Eur J Med Genet. 2007 Jan-Feb;50(1):54-9. doi: 10.1016/j.ejmg.2006.07.001. Epub 2006 Sep 10. Eur J Med Genet. 2007. PMID: 17055792

10

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. Arch Neurol. 2008 Apr;65(4):489-94. doi: 10.1001/archneur.65.4.489. Arch Neurol. 2008. PMID: 18413471 Free article.

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