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Corticopontocerebellar Connectivity Disruption in Congenital Hemiplegia.
Fiori S, Pannek K, Pasquariello R, Ware RS, Cioni G, Rose SE, Boyd RN, Guzzetta A. Fiori S, et al. Among authors: pasquariello r. Neurorehabil Neural Repair. 2015 Oct;29(9):858-66. doi: 10.1177/1545968314568726. Epub 2015 Jan 22. Neurorehabil Neural Repair. 2015. PMID: 25613985
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: pasquariello r. 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.
Neuroimaging patterns in paediatric onset hereditary spastic paraplegias.
Dosi C, Pasquariello R, Ticci C, Astrea G, Trovato R, Rubegni A, Tessa A, Cioni G, Santorelli FM, Battini R. Dosi C, et al. Among authors: pasquariello r. J Neurol Sci. 2021 Jun 15;425:117441. doi: 10.1016/j.jns.2021.117441. Epub 2021 Apr 10. J Neurol Sci. 2021. PMID: 33866115
Clinical, molecular and glycophenotype insights in SLC39A8-CDG.
Bonaventura E, Barone R, Sturiale L, Pasquariello R, Alessandrì MG, Pinto AM, Renieri A, Panteghini C, Garavaglia B, Cioni G, Battini R. Bonaventura E, et al. Among authors: pasquariello r. Orphanet J Rare Dis. 2021 Jul 10;16(1):307. doi: 10.1186/s13023-021-01941-y. Orphanet J Rare Dis. 2021. PMID: 34246313 Free PMC article.
86 results