Farrar M - Search Results

1

Diagnosis and management of children with McArdle Syndrome (GSD V) in New South Wales.

Adams L, Selvanathan A, Batten KJ, van Doorn N, Thompson S, Mitchell A, Sampaio H, Dalkeith T, Russell J, Ellaway CJ, Farrar M, Broderick C, Bhattacharya K. Adams L, et al. Among authors: farrar m. JIMD Rep. 2023 Aug 9;64(5):327-336. doi: 10.1002/jmd2.12389. eCollection 2023 Sep. JIMD Rep. 2023. PMID: 37701325 Free PMC article.

2

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. JAMA Neurol. 2016 Mar;73(3):300-7. doi: 10.1001/jamaneurol.2015.4388. JAMA Neurol. 2016. PMID: 26785318

3

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

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

4

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. Among authors: farrar m. Neurology. 2016 Jul 5;87(1):65-70. doi: 10.1212/WNL.0000000000002813. Epub 2016 Jun 8. Neurology. 2016. PMID: 27281532 Free PMC article.

5

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. Among authors: farrar m. 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.

6

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. Among authors: farrar m. Mitochondrion. 2016 Sep;30:162-7. doi: 10.1016/j.mito.2016.07.014. Epub 2016 Jul 27. Mitochondrion. 2016. PMID: 27475922

7

Polyarticular Arthritis and Spinal Muscular Atrophy in Acid Ceramidase Deficiency.

Teoh HL, Solyom A, Schuchman EH, Mowat D, Roscioli T, Farrar M, Sampaio H. Teoh HL, et al. Among authors: farrar m. Pediatrics. 2016 Oct;138(4):e20161068. doi: 10.1542/peds.2016-1068. Epub 2016 Sep 20. Pediatrics. 2016. PMID: 27650050

8

Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy.

Teoh HL, Carey K, Sampaio H, Mowat D, Roscioli T, Farrar M. Teoh HL, et al. Among authors: farrar m. Neural Plast. 2017;2017:6509493. doi: 10.1155/2017/6509493. Epub 2017 May 28. Neural Plast. 2017. PMID: 28634552 Free PMC article. Review.

9

Nusinersen for SMA: expanded access programme.

Farrar MA, Teoh HL, Carey KA, Cairns A, Forbes R, Herbert K, Holland S, Jones KJ, Menezes MP, Morrison M, Munro K, Villano D, Webster R, Woodcock IR, Yiu EM, Sampaio H, Ryan MM. Farrar MA, et al. J Neurol Neurosurg Psychiatry. 2018 Sep;89(9):937-942. doi: 10.1136/jnnp-2017-317412. Epub 2018 Mar 16. J Neurol Neurosurg Psychiatry. 2018. PMID: 29549190

10

Screening for spinal muscular atrophy.

Sampaio H, Wilcken B, Farrar M. Sampaio H, et al. Among authors: farrar m. Med J Aust. 2018 Aug 20;209(4):147-148. doi: 10.5694/mja17.00772. Med J Aust. 2018. PMID: 30107765 No abstract available.

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