D'Arrigo S - Search Results

1

Structural and connectivity parameters reveal spared connectivity in young patients with non-progressive compared to slow-progressive cerebellar ataxia.

Marchese SM, Palesi F, Nigri A, Bruzzone MG, Pantaleoni C, Gandini Wheeler-Kingshott CAM, D'Arrigo S, D'Angelo E, Cavallari P. Marchese SM, et al. Among authors: d arrigo s. Front Neurol. 2023 Oct 30;14:1279616. doi: 10.3389/fneur.2023.1279616. eCollection 2023. Front Neurol. 2023. PMID: 37965172 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. 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

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

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. 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. 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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