Riva D - Search Results

1

The syndrome of perisylvian polymicrogyria with congenital arthrogryposis.

Poduri A, Chitsazzadeh V, D'Arrigo S, Fedrizzi E, Pantaleoni C, Riva D, Busse C, Küster H, Duplessis A, Gaitanis J, Sahin M, Garganta C, Topcu M, Dies KA, Barry BJ, Partlow J, Barkovich AJ, Walsh CA, Chang BS. Poduri A, et al. Among authors: riva d, d arrigo s. Brain Dev. 2010 Aug;32(7):550-5. doi: 10.1016/j.braindev.2009.08.005. Epub 2009 Sep 13. Brain Dev. 2010. PMID: 19751967 Free PMC article.

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. Among authors: riva d, d incerti l, d arrigo s. 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. Among authors: riva d, d arrigo s. 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. Among authors: riva d, d incerti l, d arrigo s. 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

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. Among authors: riva d, d arrigo s. Pediatr Neurol. 2005 May;32(5):355-7. doi: 10.1016/j.pediatrneurol.2004.12.012. Pediatr Neurol. 2005. PMID: 15866439

6

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. Among authors: riva d. J Child Neurol. 2005 May;20(5):454-6. doi: 10.1177/08830738050200051801. J Child Neurol. 2005. PMID: 15968934

7

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. Among authors: d arrigo s. Neurol Sci. 2005 Oct;26(4):263-70. doi: 10.1007/s10072-005-0469-7. Neurol Sci. 2005. PMID: 16193253

8

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. Among authors: riva d. J Child Neurol. 2005 Nov;20(11):859-66. doi: 10.1177/08830738050200110101. J Child Neurol. 2005. PMID: 16417854

9

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. Among authors: d arrigo s. Cephalalgia. 2006 May;26(5):596-603. doi: 10.1111/j.1468-2982.2006.01072.x. Cephalalgia. 2006. PMID: 16674769

10

De novo duplication of chromosome 13(q32-q34) in a child with developmental delay.

Milani D, D'Arrigo S, Guerneri S, Selicorni A, Riva D, Pantaleoni C. Milani D, et al. Among authors: riva d, d arrigo s. J Child Neurol. 2006 Dec;21(12):1084-5. doi: 10.1177/7010.2006.00229. J Child Neurol. 2006. PMID: 17156706

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