Farrar MA - Search Results

1

The psychosocial impact of childhood dementia on children and their parents: a systematic review.

Nevin SM, McGill BC, Kelada L, Hilton G, Maack M, Elvidge KL, Farrar MA, Baynam G, Katz NT, Donovan L, Grattan S, Signorelli C, Bhattacharya K, Nunn K, Wakefield CE. Nevin SM, et al. Among authors: farrar ma. Orphanet J Rare Dis. 2023 Sep 7;18(1):277. doi: 10.1186/s13023-023-02859-3. Orphanet J Rare Dis. 2023. PMID: 37679855 Free PMC article.

2

Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease.

Menezes MP, Rahman S, Bhattacharya K, Clark D, Christodoulou J, Ellaway C, Farrar M, Pitt M, Sampaio H, Ware TL, Wedatilake Y, Thorburn DR, Ryan MM, Ouvrier R. Menezes MP, et al. Mitochondrion. 2016 Sep;30:162-7. doi: 10.1016/j.mito.2016.07.014. Epub 2016 Jul 27. Mitochondrion. 2016. PMID: 27475922

3

Parents' perceptions of power wheelchair prescription for children with a neuromuscular disorder: a scoping review.

Paguinto SG, Kasparian NA, Bray P, Farrar M. Paguinto SG, et al. Disabil Rehabil. 2019 Nov;41(23):2750-2757. doi: 10.1080/09638288.2018.1474496. Epub 2018 Jun 18. Disabil Rehabil. 2019. PMID: 29912579

4

"Getting ready for the adult world": how adults with spinal muscular atrophy perceive and experience healthcare, transition and well-being.

Wan HWY, Carey KA, D'Silva A, Kasparian NA, Farrar MA. Wan HWY, et al. Among authors: farrar ma. Orphanet J Rare Dis. 2019 Apr 2;14(1):74. doi: 10.1186/s13023-019-1052-2. Orphanet J Rare Dis. 2019. PMID: 30940178 Free PMC article.

5

Health, wellbeing and lived experiences of adults with SMA: a scoping systematic review.

Wan HWY, Carey KA, D'Silva A, Vucic S, Kiernan MC, Kasparian NA, Farrar MA. Wan HWY, et al. Among authors: farrar ma. Orphanet J Rare Dis. 2020 Mar 12;15(1):70. doi: 10.1186/s13023-020-1339-3. Orphanet J Rare Dis. 2020. PMID: 32164772 Free PMC article.

6

"We needed this": perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy.

Kariyawasam DST, D'Silva AM, Vetsch J, Wakefield CE, Wiley V, Farrar MA. Kariyawasam DST, et al. Among authors: farrar ma. EClinicalMedicine. 2021 Feb 19;33:100742. doi: 10.1016/j.eclinm.2021.100742. eCollection 2021 Mar. EClinicalMedicine. 2021. PMID: 33842861 Free PMC article.

7

The involvement of rare disease patient organisations in therapeutic innovation across rare paediatric neurological conditions: a narrative review.

Nguyen CQ, Alba-Concepcion K, Palmer EE, Scully JL, Millis N, Farrar MA. Nguyen CQ, et al. Among authors: farrar ma. Orphanet J Rare Dis. 2022 Apr 18;17(1):167. doi: 10.1186/s13023-022-02317-6. Orphanet J Rare Dis. 2022. PMID: 35436886 Free PMC article. Review.

8

Delivering paediatric precision medicine: Genomic and environmental considerations along the causal pathway of childhood neurodevelopmental disorders.

Woolfenden S, Farrar MA, Eapen V, Masi A, Wakefield CE, Badawi N, Novak I, Nassar N, Lingam R, Dale RC. Woolfenden S, et al. Among authors: farrar ma. Dev Med Child Neurol. 2022 Sep;64(9):1077-1084. doi: 10.1111/dmcn.15289. Epub 2022 Jun 6. Dev Med Child Neurol. 2022. PMID: 35661141 Free PMC article. Review.

9

'Advocacy groups are the connectors': Experiences and contributions of rare disease patient organization leaders in advanced neurotherapeutics.

Nguyen CQ, Kariyawasam D, Alba-Concepcion K, Grattan S, Hetherington K, Wakefield CE, Woolfenden S, Dale RC, Palmer EE, Farrar MA. Nguyen CQ, et al. Among authors: farrar ma. Health Expect. 2022 Dec;25(6):3175-3191. doi: 10.1111/hex.13625. Epub 2022 Oct 28. Health Expect. 2022. PMID: 36307981 Free PMC article.

10

Newborn Screening for the Diagnosis and Treatment of Duchenne Muscular Dystrophy.

Farrar MA, Kariyawasam D, Grattan S, Bayley K, Davis M, Holland S, Waddel LB, Jones K, Lorentzos M, Ravine A, Wotton T, Wiley V; DMD NBS Working Group. Farrar MA, et al. J Neuromuscul Dis. 2023;10(1):15-28. doi: 10.3233/JND-221535. J Neuromuscul Dis. 2023. PMID: 36373292 Free PMC article. Review.

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