Farrar M - Search Results

1

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

2

Axonal dysfunction, dysmyelination, and conduction failure in hereditary neuropathy with liability to pressure palsies.

Farrar MA, Park SB, Krishnan AV, Kiernan MC, Lin CS. Farrar MA, et al. Muscle Nerve. 2014 Jun;49(6):858-65. doi: 10.1002/mus.24085. Muscle Nerve. 2014. PMID: 24752454

3

Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporter.

Menezes MP, Farrar MA, Webster R, Antony J, O'Brien K, Ouvrier R, Kiernan MC, Burns J, Vucic S. Menezes MP, et al. Clin Neurophysiol. 2016 Jan;127(1):911-918. doi: 10.1016/j.clinph.2015.05.012. Epub 2015 Jun 3. Clin Neurophysiol. 2016. PMID: 26092362

4

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

5

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

6

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.

7

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.

8

Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.

Brewer MH, Chaudhry R, Qi J, Kidambi A, Drew AP, Menezes MP, Ryan MM, Farrar MA, Mowat D, Subramanian GM, Young HK, Zuchner S, Reddel SW, Nicholson GA, Kennerson ML. Brewer MH, et al. Among authors: farrar ma. PLoS Genet. 2016 Jul 20;12(7):e1006177. doi: 10.1371/journal.pgen.1006177. eCollection 2016 Jul. PLoS Genet. 2016. PMID: 27438001 Free PMC article.

9

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

10

Pediatric chemotherapy induced peripheral neuropathy: A systematic review of current knowledge.

Kandula T, Park SB, Cohn RJ, Krishnan AV, Farrar MA. Kandula T, et al. Cancer Treat Rev. 2016 Nov;50:118-128. doi: 10.1016/j.ctrv.2016.09.005. Epub 2016 Sep 10. Cancer Treat Rev. 2016. PMID: 27664395 Review.

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