Borgatti R - Search Results

1

Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients.

Borgatti R, Piccinelli P, Passoni D, Dalprà L, Miozzo M, Micheli R, Gagliardi C, Balottin U. Borgatti R, et al. Pediatr Neurol. 2001 Feb;24(2):111-6. doi: 10.1016/s0887-8994(00)00244-7. Pediatr Neurol. 2001. PMID: 11275459

2

Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15.

Borgatti R, Piccinelli P, Passoni D, Raggi E, Ferrarese C. Borgatti R, et al. J Child Neurol. 2001 Dec;16(12):911-4. doi: 10.1177/088307380101601209. J Child Neurol. 2001. PMID: 11785506

3

Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome.

Borgatti R, Piccinelli P, Passoni D, Romeo A, Viri M, Musumeci SA, Elia M, Cogliati T, Valseriati D, Grasso R, Raggi ME, Ferrarese C. Borgatti R, et al. J Child Neurol. 2003 Jan;18(1):21-5. doi: 10.1177/08830738030180010801. J Child Neurol. 2003. PMID: 12661934

4

Agenesis of the corpus callosum: clinical and genetic study in 63 young patients.

Bedeschi MF, Bonaglia MC, Grasso R, Pellegri A, Garghentino RR, Battaglia MA, Panarisi AM, Di Rocco M, Balottin U, Bresolin N, Bassi MT, Borgatti R. Bedeschi MF, et al. Among authors: borgatti r. Pediatr Neurol. 2006 Mar;34(3):186-93. doi: 10.1016/j.pediatrneurol.2005.08.008. Pediatr Neurol. 2006. PMID: 16504787

5

Evolution of neurologic features in Williams syndrome.

Gagliardi C, Martelli S, Burt MD, Borgatti R. Gagliardi C, et al. Among authors: borgatti r. Pediatr Neurol. 2007 May;36(5):301-6. doi: 10.1016/j.pediatrneurol.2007.01.001. Pediatr Neurol. 2007. PMID: 17509461

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. J Child Neurol. 2004 Jul;19(7):509-15. doi: 10.1177/08830738040190070601. J Child Neurol. 2004. PMID: 15526955

7

Bilateral perisylvian polymicrogyria in three generations.

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

8

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome.

Bonaglia MC, Giorda R, Borgatti R, Felisari G, Gagliardi C, Selicorni A, Zuffardi O. Bonaglia MC, et al. Among authors: borgatti r. Am J Hum Genet. 2001 Aug;69(2):261-8. doi: 10.1086/321293. Epub 2001 Jun 18. Am J Hum Genet. 2001. PMID: 11431708 Free PMC article.

9

Sequence learning in cerebral palsy.

Gagliardi C, Tavano A, Turconi AC, Pozzoli U, Borgatti R. Gagliardi C, et al. Among authors: borgatti r. Pediatr Neurol. 2011 Mar;44(3):207-13. doi: 10.1016/j.pediatrneurol.2010.10.004. Pediatr Neurol. 2011. PMID: 21310337

10

Seckel's syndrome and malformations of cortical development: report of three new cases and review of the literature.

Capovilla G, Lorenzetti ME, Montagnini A, Borgatti R, Piccinelli P, Giordano L, Accorsi P, Caudana R. Capovilla G, et al. Among authors: borgatti r. J Child Neurol. 2001 May;16(5):382-6. doi: 10.1177/088307380101600516. J Child Neurol. 2001. PMID: 11392528

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