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314 results

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Development and Pilot Study of a Pediatric Screening for Feeding and Swallowing Disorders in Infants and Children: The Pediatric Screening-Priority Evaluation Dysphagia (PS-PED).
Cerchiari A, Tofani M, Giordani C, Franceschetti S, Capuano E, Pizza F, Della Bella G, Raponi M, Biondo G. Cerchiari A, et al. Among authors: franceschetti s. Children (Basel). 2023 Mar 29;10(4):638. doi: 10.3390/children10040638. Children (Basel). 2023. PMID: 37189887 Free PMC article.
Early occurrence of photic-reflex myoclonus in CDKL5-deficiency disorder.
Caputo D, Franceschetti S, Canafoglia L, Iascone M, Rossi Sebastiano D, Freri E, Granata T. Caputo D, et al. Among authors: franceschetti s. Clin Neurophysiol. 2024 Apr 17;163:37-38. doi: 10.1016/j.clinph.2024.04.007. Online ahead of print. Clin Neurophysiol. 2024. PMID: 38691984 No abstract available.
Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a Patient with NAA15 Variant.
Freri E, Canafoglia L, Ciaccio C, Rossi Sebastiano D, Caputo D, Solazzi R, Sciacca FL, Iascone M, Panzica F, Granata T, Franceschetti S, Nardocci N. Freri E, et al. Among authors: franceschetti s. Mov Disord. 2024 Apr 21. doi: 10.1002/mds.29793. Online ahead of print. Mov Disord. 2024. PMID: 38643413 No abstract available.
Correlation between autistic traits and brain functional connectivity in preschoolers with autism spectrum disorder: a resting state MEG study.
Taddei M, Cuesta P, Annunziata S, Bulgheroni S, Esposito S, Visani E, Granvillano A, Dotta S, Rossi DS, Panzica F, Franceschetti S, Varotto G, Riva D. Taddei M, et al. Among authors: franceschetti s. Neurol Sci. 2024 Apr 19. doi: 10.1007/s10072-024-07528-2. Online ahead of print. Neurol Sci. 2024. PMID: 38639894
Myoclonus: Differential diagnosis and current management.
Riva A, D'Onofrio G, Ferlazzo E, Pascarella A, Pasini E, Franceschetti S, Panzica F, Canafoglia L, Vignoli A, Coppola A, Badioni V, Beccaria F, Labate A, Gambardella A, Romeo A, Capovilla G, Michelucci R, Striano P, Belcastro V. Riva A, et al. Among authors: franceschetti s. Epilepsia Open. 2024 Apr;9(2):486-500. doi: 10.1002/epi4.12917. Epub 2024 Feb 9. Epilepsia Open. 2024. PMID: 38334331 Free PMC article. Review.
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations.
Tsai MH, Ke HC, Lin WC, Nian FS, Huang CW, Cheng HY, Hsu CS, Granata T, Chang CH, Castellotti B, Lin SY, Doniselli FM, Lu CJ, Franceschetti S, Ragona F, Hou PS, Canafoglia L, Tung CY, Lee MH, Wang WJ, Tsai JW. Tsai MH, et al. Among authors: franceschetti s. Acta Neuropathol. 2024 Jan 9;147(1):13. doi: 10.1007/s00401-023-02665-y. Acta Neuropathol. 2024. PMID: 38194050 Free PMC article.
Myoclonus in genetic Alzheimer's disease due to presenilin-1 mutation.
Uccellini D, Canafoglia L, Franceschetti S, Stabile A, Catania M, Tagliavini F, Giaccone G, Di Fede G. Uccellini D, et al. Among authors: franceschetti s. Clin Neurophysiol. 2023 Dec;156:86-88. doi: 10.1016/j.clinph.2023.10.002. Epub 2023 Oct 16. Clin Neurophysiol. 2023. PMID: 37897907 No abstract available.
314 results