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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2014 2
2015 1
2016 2
2017 2
2018 3
2019 5
2020 6
2021 2
2022 0
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21 results
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Page 1
Dysarthria and broader motor speech deficits in Dravet syndrome.
Turner SJ, Brown A, Arpone M, Anderson V, Morgan AT, Scheffer IE. Turner SJ, et al. Among authors: arpone m. Neurology. 2017 Feb 21;88(8):743-749. doi: 10.1212/WNL.0000000000003635. Epub 2017 Feb 1. Neurology. 2017. PMID: 28148630 Free PMC article.
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.
Baker EK, Arpone M, Vera SA, Bretherton L, Ure A, Kraan CM, Bui M, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field MJ, Cohen J, Maria LS, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE. Baker EK, et al. Among authors: arpone m. J Neurodev Disord. 2019 Dec 26;11(1):41. doi: 10.1186/s11689-019-9288-7. J Neurodev Disord. 2019. PMID: 31878865 Free PMC article.
PediAppRREST: effectiveness of an interactive cognitive support tablet app in reducing deviations from guidelines in the management of paediatric cardiac arrest: protocol for a simulation-based randomised controlled trial.
Corazza F, Arpone M, Snijders D, Cheng A, Stritoni V, Ingrassia PL, De Luca M, Tortorolo L, Frigo AC, Da Dalt L, Bressan S. Corazza F, et al. Among authors: arpone m. BMJ Open. 2021 Jul 28;11(7):e047208. doi: 10.1136/bmjopen-2020-047208. BMJ Open. 2021. PMID: 34321297 Free PMC article.
FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome.
Baker EK, Arpone M, Kraan C, Bui M, Rogers C, Field M, Bretherton L, Ling L, Ure A, Cohen J, Hunter MF, Santa María L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende A, Amor DJ, Godler DE. Baker EK, et al. Among authors: arpone m. Sci Rep. 2020 Jul 16;10(1):11701. doi: 10.1038/s41598-020-68465-6. Sci Rep. 2020. PMID: 32678152 Free PMC article.
Accuracy of NEXUS II head injury decision rule in children: a prospective PREDICT cohort study.
Babl FE, Oakley E, Dalziel SR, Borland ML, Phillips N, Kochar A, Dalton S, Cheek JA, Gilhotra Y, Furyk J, Neutze J, Donath S, Hearps S, Crowe LM, Arpone M, Bressan S, Lyttle MD; Paediatric Research in Emergency Department International Collaborative (PREDICT). Babl FE, et al. Among authors: arpone m. Emerg Med J. 2019 Jan;36(1):4-11. doi: 10.1136/emermed-2017-207435. Epub 2018 Aug 20. Emerg Med J. 2019. PMID: 30127072
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.
Baker EK, Arpone M, Aliaga SM, Bretherton L, Kraan CM, Bui M, Slater HR, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field M, Cohen J, Cornish K, Santa Maria L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE. Baker EK, et al. Among authors: arpone m. Mol Autism. 2019 May 3;10:21. doi: 10.1186/s13229-019-0271-7. eCollection 2019. Mol Autism. 2019. PMID: 31073396 Free PMC article.
21 results