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Penetrating head injuries in children presenting to the emergency department in Australia and New Zealand: A PREDICT prospective study.
Babl FE, Lyttle MD, Bressan S, Borland ML, Phillips N, Kochar A, Dalton S, Cheek JA, Gilhotra Y, Furyk J, Neutze J, Donath S, Hearps S, Arpone M, Crowe L, Dalziel SR, Barker R, Oakley E. Babl FE, et al. Among authors: arpone m. J Paediatr Child Health. 2018 Aug;54(8):861-865. doi: 10.1111/jpc.13903. Epub 2018 Mar 26. J Paediatr Child Health. 2018. PMID: 29579354
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
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.
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X.
Arpone M, Baker EK, Bretherton L, Bui M, Li X, Whitaker S, Dissanayake C, Cohen J, Hickerton C, Rogers C, Field M, Elliott J, Aliaga SM, Ling L, Francis D, Hearps SJC, Hunter MF, Amor DJ, Godler DE. Arpone M, et al. Sci Rep. 2018 Feb 26;8(1):3644. doi: 10.1038/s41598-018-21990-x. Sci Rep. 2018. PMID: 29483611 Free PMC article.
Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia.
Hwang YT, Dudding T, Aliaga SM, Arpone M, Francis D, Li X, Slater HR, Rogers C, Bretherton L, du Sart D, Heard R, Godler DE. Hwang YT, et al. Among authors: arpone m. Genes (Basel). 2016 Sep 21;7(9):68. doi: 10.3390/genes7090068. Genes (Basel). 2016. PMID: 27657133 Free PMC article.
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.
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