Pantaleoni C - Search Results

1

Novel mutations in TSEN54 in pontocerebellar hypoplasia type 2.

Battini R, D'Arrigo S, Cassandrini D, Guzzetta A, Fiorillo C, Pantaleoni C, Romano A, Alfei E, Cioni G, Santorelli FM. Battini R, et al. Among authors: pantaleoni c. J Child Neurol. 2014 Apr;29(4):520-5. doi: 10.1177/0883073812470002. Epub 2013 Jan 9. J Child Neurol. 2014. PMID: 23307886

2

Developmental profiles of young children with autism spectrum disorder and global developmental delay: A study with the Griffiths III scales.

Taddei M, Bulgheroni S, Toffalini E, Pantaleoni C, Lanfranchi S. Taddei M, et al. Among authors: pantaleoni c. Autism Res. 2023 Jul;16(7):1344-1359. doi: 10.1002/aur.2953. Epub 2023 Jun 1. Autism Res. 2023. PMID: 37260303

3

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

4

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. Among authors: pantaleoni c. Brain Dev. 2004 Jun;26(4):273-80. doi: 10.1016/S0387-7604(03)00130-X. Brain Dev. 2004. PMID: 15130695

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: pantaleoni c. 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: pantaleoni c. J Child Neurol. 2005 May;20(5):454-6. doi: 10.1177/08830738050200051801. J Child Neurol. 2005. PMID: 15968934

7

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: pantaleoni c. J Child Neurol. 2005 Nov;20(11):859-66. doi: 10.1177/08830738050200110101. J Child Neurol. 2005. PMID: 16417854

8

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: pantaleoni c. J Child Neurol. 2006 Dec;21(12):1084-5. doi: 10.1177/7010.2006.00229. J Child Neurol. 2006. PMID: 17156706

9

Craniodigital syndrome of Scott: clinical and neuroradiological features of a new case.

Milani D, D'Arrigo S, Erbetta A, Selicorni A, Riva D, Pantaleoni C. Milani D, et al. Among authors: pantaleoni c. J Child Neurol. 2007 Jul;22(7):883-6. doi: 10.1177/0883073807304195. J Child Neurol. 2007. PMID: 17715284

10

Verbal and gestural communication in children with bilateral perisylvian polymicrogyria.

Saletti V, Bulgheroni S, D'Incerti L, Franceschetti S, Molteni B, Airaghi G, Pantaleoni C, D'Arrigo S, Riva D. Saletti V, et al. Among authors: pantaleoni c. J Child Neurol. 2007 Sep;22(9):1090-8. doi: 10.1177/0883073807306247. J Child Neurol. 2007. PMID: 17890406

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

129 results

Search Page

Filters