D'Arrigo S - Search Results

1

The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders.

Rizzo A, Alfei E, Zibordi F, Saletti V, Zorzi G, Freri E, Estienne M, Girgenti V, D'Arrigo S, Esposito S, Buldrini B, Moroni I, Milani D, Granata T, Ardissone A, Eoli M, Molteni B, Bigoni S, Pantaleoni C, Nardocci N, Sciacca FL. Rizzo A, et al. Am J Med Genet B Neuropsychiatr Genet. 2018 Sep;177(6):557-562. doi: 10.1002/ajmg.b.32649. Epub 2018 Aug 14. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 30105822

2

A case of 3-methylglutaconic aciduria misdiagnosed as cerebral palsy.

Pantaleoni C, D'Arrigo S, D'Incerti L, Rimoldi M, Riva D. Pantaleoni C, et al. Pediatr Neurol. 2000 Nov;23(5):442-4. doi: 10.1016/s0887-8994(00)00217-4. Pediatr Neurol. 2000. PMID: 11118804

3

Papillitis as an onset sign of Leber's hereditary optic neuropathy: a case report.

Pantaleoni C, D'Arrigo S, Bagnasco I, Piozzi E, Carrara F, Scaioli V, Riva D. Pantaleoni C, et al. Brain Dev. 2001 Mar;23(2):125-7. doi: 10.1016/s0387-7604(01)00185-1. Brain Dev. 2001. PMID: 11248462

4

Oligoyric microcephaly in a child with Williams syndrome.

Faravelli F, D'Arrigo S, Bagnasco I, Selicorni A, D'Incerti L, Riva D, Pantaleoni C. Faravelli F, et al. Am J Med Genet A. 2003 Mar 1;117A(2):169-71. doi: 10.1002/ajmg.a.10892. Am J Med Genet A. 2003. PMID: 12567416

5

Unusual neurophysiological features in Cockayne's syndrome: a report of two cases as a contribution to diagnosis and classification.

Scaioli V, D'Arrigo S, Pantaleoni C. Scaioli V, et al. Brain Dev. 2004 Jun;26(4):273-80. doi: 10.1016/S0387-7604(03)00130-X. Brain Dev. 2004. PMID: 15130695

6

Another patient with MECP2 mutation without classic Rett syndrome phenotype.

Milani D, Pantaleoni C, D'Arrigo S, Selicorni A, Riva D. Milani D, et al. Pediatr Neurol. 2005 May;32(5):355-7. doi: 10.1016/j.pediatrneurol.2004.12.012. Pediatr Neurol. 2005. PMID: 15866439

7

Progressive encephalopathy with edema, hypsarrhythmia, and optic nerve atrophy (PEHO)-like syndrome: what diagnostic characteristics are defining?

D'Arrigo S, Grazia BM, Faravelli F, Riva D, Pantaleoni C. D'Arrigo S, et al. J Child Neurol. 2005 May;20(5):454-6. doi: 10.1177/08830738050200051801. J Child Neurol. 2005. PMID: 15968934

8

Unilateral frontal lobe epilepsy affects executive functions in children.

Riva D, Avanzini G, Franceschetti S, Nichelli F, Saletti V, Vago C, Pantaleoni C, D'Arrigo S, Andreucci E, Aggio F, Paruta N, Bulgheroni S. Riva D, et al. Neurol Sci. 2005 Oct;26(4):263-70. doi: 10.1007/s10072-005-0469-7. Neurol Sci. 2005. PMID: 16193253

9

Diagnostic approach to cerebellar disease in children.

D'Arrigo S, Viganò L, Grazia Bruzzone M, Marzaroli M, Nikas I, Riva D, Pantaleoni C. D'Arrigo S, et al. J Child Neurol. 2005 Nov;20(11):859-66. doi: 10.1177/08830738050200110101. J Child Neurol. 2005. PMID: 16417854

10

Cognitive and behavioural effects of migraine in childhood and adolescence.

Riva D, Aggio F, Vago C, Nichelli F, Andreucci E, Paruta N, D'Arrigo S, Pantaleoni C, Bulgheroni S. Riva D, et al. Cephalalgia. 2006 May;26(5):596-603. doi: 10.1111/j.1468-2982.2006.01072.x. Cephalalgia. 2006. PMID: 16674769

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