Ouvrier RA - Search Results

1

Autosomal dominant congenital spinal muscular atrophy--a possible developmental deficiency of motor neurones?

Reddel S, Ouvrier RA, Nicholson G, Dierick I, Irobi J, Timmerman V, Ryan MM. Reddel S, et al. Among authors: ouvrier ra. Neuromuscul Disord. 2008 Jul;18(7):530-5. doi: 10.1016/j.nmd.2008.04.016. Epub 2008 Jun 24. Neuromuscul Disord. 2008. PMID: 18579380 Review.

2

Hand involvement in children with Charcot-Marie-Tooth disease type 1A.

Burns J, Bray P, Cross LA, North KN, Ryan MM, Ouvrier RA. Burns J, et al. Among authors: ouvrier ra. Neuromuscul Disord. 2008 Dec;18(12):970-3. doi: 10.1016/j.nmd.2008.08.004. Epub 2008 Nov 6. Neuromuscul Disord. 2008. PMID: 18993073

3

Establishment of the Australasian paediatric Charcot-Marie-Tooth disease registry.

Burns J, Ouvrier RA, Nicholson GA, Ryan MM. Burns J, et al. Among authors: ouvrier ra. Neuromuscul Disord. 2007 Apr;17(4):349-50. doi: 10.1016/j.nmd.2006.11.007. Epub 2007 Feb 15. Neuromuscul Disord. 2007. PMID: 17416318 No abstract available.

4

Childhood chronic inflammatory demyelinating polyneuropathy: clinical course and long-term outcome.

Ryan MM, Grattan-Smith PJ, Procopis PG, Morgan G, Ouvrier RA. Ryan MM, et al. Among authors: ouvrier ra. Neuromuscul Disord. 2000 Aug;10(6):398-406. doi: 10.1016/s0960-8966(00)00119-x. Neuromuscul Disord. 2000. PMID: 10899445 Clinical Trial.

5

Anterior horn cell disease and olivopontocerebellar hypoplasia.

Ryan MM, Cooke-Yarborough CM, Procopis PG, Ouvrier RA. Ryan MM, et al. Among authors: ouvrier ra. Pediatr Neurol. 2000 Aug;23(2):180-4. doi: 10.1016/s0887-8994(00)00166-1. Pediatr Neurol. 2000. PMID: 11020648

6

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.

7

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

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

8

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: ouvrier ra. Neurology. 2008 May 6;70(19):1678-81. doi: 10.1212/01.wnl.0000311275.89032.22. Neurology. 2008. PMID: 18458227

9

Peripheral neuropathy in cardiofaciocutaneous syndrome.

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

10

Evolution of foot and ankle manifestations in children with CMT1A.

Burns J, Ryan MM, Ouvrier RA. Burns J, et al. Among authors: ouvrier ra. Muscle Nerve. 2009 Feb;39(2):158-66. doi: 10.1002/mus.21140. Muscle Nerve. 2009. PMID: 19145658

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