Farrar MA - Search Results

1

Onasemnogene abeparvovec in spinal muscular atrophy: an Australian experience of safety and efficacy.

D'Silva AM, Holland S, Kariyawasam D, Herbert K, Barclay P, Cairns A, MacLennan SC, Ryan MM, Sampaio H, Smith N, Woodcock IR, Yiu EM, Alexander IE, Farrar MA. D'Silva AM, et al. Among authors: farrar ma. Ann Clin Transl Neurol. 2022 Mar;9(3):339-350. doi: 10.1002/acn3.51519. Epub 2022 Feb 16. Ann Clin Transl Neurol. 2022. PMID: 35170254 Free PMC article.

2

Spinal muscular atrophy: molecular mechanisms.

Farrar MA, Johnston HM, Grattan-Smith P, Turner A, Kiernan MC. Farrar MA, et al. Curr Mol Med. 2009 Sep;9(7):851-62. doi: 10.2174/156652409789105516. Curr Mol Med. 2009. PMID: 19860664 Review.

3

Dysfunction of axonal membrane conductances in adolescents and young adults with spinal muscular atrophy.

Farrar MA, Vucic S, Lin CS, Park SB, Johnston HM, du Sart D, Bostock H, Kiernan MC. Farrar MA, et al. Brain. 2011 Nov;134(Pt 11):3185-97. doi: 10.1093/brain/awr229. Epub 2011 Sep 16. Brain. 2011. PMID: 21926101 Free PMC article.

4

Corticomotoneuronal integrity and adaptation in spinal muscular atrophy.

Farrar MA, Vucic S, Johnston HM, Kiernan MC. Farrar MA, et al. Arch Neurol. 2012 Apr;69(4):467-73. doi: 10.1001/archneurol.2011.1697. Arch Neurol. 2012. PMID: 22491191

5

Pathophysiological insights derived by natural history and motor function of spinal muscular atrophy.

Farrar MA, Vucic S, Johnston HM, du Sart D, Kiernan MC. Farrar MA, et al. J Pediatr. 2013 Jan;162(1):155-9. doi: 10.1016/j.jpeds.2012.05.067. Epub 2012 Jul 17. J Pediatr. 2013. PMID: 22809660 Free article.

6

The Genetics of Spinal Muscular Atrophy: Progress and Challenges.

Farrar MA, Kiernan MC. Farrar MA, et al. Neurotherapeutics. 2015 Apr;12(2):290-302. doi: 10.1007/s13311-014-0314-x. Neurotherapeutics. 2015. PMID: 25413156 Free PMC article. Review.

7

Clinical Characteristics and Functional Motor Outcomes of Enterovirus 71 Neurological Disease in Children.

Teoh HL, Mohammad SS, Britton PN, Kandula T, Lorentzos MS, Booy R, Jones CA, Rawlinson W, Ramachandran V, Rodriguez ML, Andrews PI, Dale RC, Farrar MA, Sampaio H. Teoh HL, et al. Among authors: farrar ma. JAMA Neurol. 2016 Mar;73(3):300-7. doi: 10.1001/jamaneurol.2015.4388. JAMA Neurol. 2016. PMID: 26785318

8

Fracture in Duchenne Muscular Dystrophy: Natural History and Vitamin D Deficiency.

Perera N, Sampaio H, Woodhead H, Farrar M. Perera N, et al. J Child Neurol. 2016 Aug;31(9):1181-7. doi: 10.1177/0883073816650034. Epub 2016 May 24. J Child Neurol. 2016. PMID: 27221372

9

Novel motor phenotypes in patients with VRK1 mutations without pontocerebellar hypoplasia.

Stoll M, Teoh H, Lee J, Reddel S, Zhu Y, Buckley M, Sampaio H, Roscioli T, Farrar M, Nicholson G. Stoll M, et al. Neurology. 2016 Jul 5;87(1):65-70. doi: 10.1212/WNL.0000000000002813. Epub 2016 Jun 8. Neurology. 2016. PMID: 27281532 Free PMC article.

10

Approaches to genetic diagnosis in neuromuscular conditions in the era of next generation sequencing.

Teoh HL, Sampaio H, Roscioli T, Farrar M. Teoh HL, et al. J Neurol Neurosurg Psychiatry. 2016 Dec;87(12):1384-1385. doi: 10.1136/jnnp-2016-313812. Epub 2016 Jun 14. J Neurol Neurosurg Psychiatry. 2016. PMID: 27301348 No abstract available.

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