Ryan MM - Search Results

1

Hereditary peripheral neuropathies of childhood.

Ryan MM, Ouvrier R. Ryan MM, et al. Curr Opin Neurol. 2005 Apr;18(2):105-10. doi: 10.1097/01.wco.0000162849.37273.af. Curr Opin Neurol. 2005. PMID: 15791138 Review.

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

3

Autosomal-recessive and X-linked forms of hereditary motor and sensory neuropathy in childhood.

Ouvrier R, Geevasingha N, Ryan MM. Ouvrier R, et al. Among authors: ryan mm. Muscle Nerve. 2007 Aug;36(2):131-43. doi: 10.1002/mus.20776. Muscle Nerve. 2007. PMID: 17410579 Review.

4

Peripheral neuropathy in cardiofaciocutaneous syndrome.

DeRoos ST, Ryan MM, Ouvrier RA. DeRoos ST, et al. Among authors: ryan mm. Pediatr Neurol. 2007 Apr;36(4):250-2. doi: 10.1016/j.pediatrneurol.2006.12.004. Pediatr Neurol. 2007. PMID: 17437909

5

Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations.

Nicholson GA, Magdelaine C, Zhu D, Grew S, Ryan MM, Sturtz F, Vallat JM, Ouvrier RA. Nicholson GA, et al. Among authors: ryan mm. Neurology. 2008 May 6;70(19):1678-81. doi: 10.1212/01.wnl.0000311275.89032.22. Neurology. 2008. PMID: 18458227

6

Ascorbic acid for Charcot-Marie-Tooth disease type 1A in children: a randomised, double-blind, placebo-controlled, safety and efficacy trial.

Burns J, Ouvrier RA, Yiu EM, Joseph PD, Kornberg AJ, Fahey MC, Ryan MM. Burns J, et al. Among authors: ryan mm. Lancet Neurol. 2009 Jun;8(6):537-44. doi: 10.1016/S1474-4422(09)70108-5. Epub 2009 May 6. Lancet Neurol. 2009. PMID: 19427269 Clinical Trial.

7

Quality of life in children with Charcot-Marie-Tooth disease.

Burns J, Ryan MM, Ouvrier RA. Burns J, et al. Among authors: ryan mm. J Child Neurol. 2010 Mar;25(3):343-7. doi: 10.1177/0883073809339877. Epub 2009 Aug 27. J Child Neurol. 2010. PMID: 19713553

8

Effect of oral curcumin on Déjérine-Sottas disease.

Burns J, Joseph PD, Rose KJ, Ryan MM, Ouvrier RA. Burns J, et al. Among authors: ryan mm. Pediatr Neurol. 2009 Oct;41(4):305-8. doi: 10.1016/j.pediatrneurol.2009.04.030. Pediatr Neurol. 2009. PMID: 19748054 Clinical Trial.

9

Muscle cramp in pediatric Charcot-Marie-Tooth disease type 1A: prevalence and predictors.

Blyton F, Ryan MM, Ouvrier RA, Burns J. Blyton F, et al. Among authors: ryan mm. Neurology. 2011 Dec 13;77(24):2115-8. doi: 10.1212/WNL.0b013e31823d76aa. Epub 2011 Nov 30. Neurology. 2011. PMID: 22131544 Free PMC article.

10

Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.

Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, Grew S, Ryan MM, Funalot B. Vallat JM, et al. Among authors: ryan mm. J Neuropathol Exp Neurol. 2008 Nov;67(11):1097-102. doi: 10.1097/NEN.0b013e31818b6cbc. J Neuropathol Exp Neurol. 2008. PMID: 18957892

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