Chilosi A - Search Results

1

Evidence for a Pathogenic Role of CSMD1 in Childhood Apraxia of Speech.

Formicola D, Podda I, Pantaleo M, Andreucci E, Lopergolo D, Giglio S, Santorelli FM, Chilosi A. Formicola D, et al. Among authors: chilosi a. Neuropediatrics. 2023 Dec;54(6):407-411. doi: 10.1055/s-0043-1771033. Epub 2023 Aug 7. Neuropediatrics. 2023. PMID: 37549685

2

Neural Changes Induced by a Speech Motor Treatment in Childhood Apraxia of Speech: A Case Series.

Fiori S, Pannek K, Podda I, Cipriani P, Lorenzoni V, Franchi B, Pasquariello R, Guzzetta A, Cioni G, Chilosi A. Fiori S, et al. Among authors: chilosi a. J Child Neurol. 2021 Oct;36(11):958-967. doi: 10.1177/08830738211015800. Epub 2021 Jul 28. J Child Neurol. 2021. PMID: 34315296 Free PMC article.

3

Implicit learning in children with Childhood Apraxia of Speech.

Bombonato C, Casalini C, Pecini C, Angelucci G, Vicari S, Podda I, Cipriani P, Chilosi AM, Menghini D. Bombonato C, et al. Among authors: chilosi am. Res Dev Disabil. 2022 Mar;122:104170. doi: 10.1016/j.ridd.2021.104170. Epub 2022 Jan 11. Res Dev Disabil. 2022. PMID: 35030467

4

Neuroanatomical correlates of childhood apraxia of speech: A connectomic approach.

Fiori S, Guzzetta A, Mitra J, Pannek K, Pasquariello R, Cipriani P, Tosetti M, Cioni G, Rose SE, Chilosi A. Fiori S, et al. Among authors: chilosi a. Neuroimage Clin. 2016 Nov 4;12:894-901. doi: 10.1016/j.nicl.2016.11.003. eCollection 2016. Neuroimage Clin. 2016. PMID: 27882295 Free PMC article.

5

Autism Spectrum Disorder and Childhood Apraxia of Speech: Early Language-Related Hallmarks across Structural MRI Study.

Conti E, Retico A, Palumbo L, Spera G, Bosco P, Biagi L, Fiori S, Tosetti M, Cipriani P, Cioni G, Muratori F, Chilosi A, Calderoni S. Conti E, et al. Among authors: chilosi a. J Pers Med. 2020 Dec 12;10(4):275. doi: 10.3390/jpm10040275. J Pers Med. 2020. PMID: 33322765 Free PMC article.

6

Vowel variability and contrast in Childhood Apraxia of Speech: acoustics and articulation.

Lenoci G, Celata C, Ricci I, Chilosi A, Barone V. Lenoci G, et al. Among authors: chilosi a. Clin Linguist Phon. 2021 Nov 2;35(11):1011-1035. doi: 10.1080/02699206.2020.1853811. Epub 2020 Dec 16. Clin Linguist Phon. 2021. PMID: 33322970

7

Mental retardation and verbal dyspraxia in a new patient with de novo creatine transporter (SLC6A8) mutation.

Battini R, Chilosi A, Mei D, Casarano M, Alessandrì MG, Leuzzi V, Ferretti G, Tosetti M, Bianchi MC, Cioni G. Battini R, et al. Among authors: chilosi a. Am J Med Genet A. 2007 Aug 1;143A(15):1771-4. doi: 10.1002/ajmg.a.31827. Am J Med Genet A. 2007. PMID: 17603797

8

Treatment with L-arginine improves neuropsychological disorders in a child with creatine transporter defect.

Chilosi A, Leuzzi V, Battini R, Tosetti M, Ferretti G, Comparini A, Casarano M, Moretti E, Alessandri MG, Bianchi MC, Cioni G. Chilosi A, et al. Neurocase. 2008;14(2):151-61. doi: 10.1080/13554790802060821. Neurocase. 2008. PMID: 18569740

9

Neurodevelopmental disorders in children with severe to profound sensorineural hearing loss: a clinical study.

Chilosi AM, Comparini A, Scusa MF, Berrettini S, Forli F, Battini R, Cipriani P, Cioni G. Chilosi AM, et al. Dev Med Child Neurol. 2010 Sep;52(9):856-62. doi: 10.1111/j.1469-8749.2010.03621.x. Epub 2010 Mar 19. Dev Med Child Neurol. 2010. PMID: 20345959 Free article.

10

Hemispheric specialization for language in children with different types of specific language impairment.

Pecini C, Casalini C, Brizzolara D, Cipriani P, Pfanner L, Chilosi A. Pecini C, et al. Among authors: chilosi a. Cortex. 2005 Apr;41(2):157-67. doi: 10.1016/s0010-9452(08)70890-6. Cortex. 2005. PMID: 15714898 Clinical Trial.

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