Ryan MM - Search Results

1

Development and validation of the Charcot-Marie-Tooth Disease Infant Scale.

Mandarakas MR, Menezes MP, Rose KJ, Shy R, Eichinger K, Foscan M, Estilow T, Kennedy R, Herbert K, Bray P, Refshauge K, Ryan MM, Yiu EM, Farrar M, Sampaio H, Moroni I, Pagliano E, Pareyson D, Yum SW, Herrmann DN, Acsadi G, Shy ME, Burns J, Sanmaneechai O. Mandarakas MR, et al. Among authors: ryan mm. Brain. 2018 Dec 1;141(12):3319-3330. doi: 10.1093/brain/awy280. Brain. 2018. PMID: 30476010 Free PMC article.

2

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

Burns J, Ouvrier RA, Nicholson GA, Ryan MM. Burns J, et al. Among authors: ryan mm. 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.

3

Interventions for the prevention and treatment of pes cavus.

Burns J, Landorf KB, Ryan MM, Crosbie J, Ouvrier RA. Burns J, et al. Among authors: ryan mm. Cochrane Database Syst Rev. 2007 Oct 17;2007(4):CD006154. doi: 10.1002/14651858.CD006154.pub2. Cochrane Database Syst Rev. 2007. PMID: 17943889 Free PMC article. Review.

4

Reliability of quantifying foot and ankle muscle strength in very young children.

Rose KJ, Burns J, Ryan MM, Ouvrier RA, North KN. Rose KJ, et al. Among authors: ryan mm. Muscle Nerve. 2008 May;37(5):626-31. doi: 10.1002/mus.20961. Muscle Nerve. 2008. PMID: 18236461

5

Central nervous system signs in X-linked Charcot-Marie-Tooth disease after hyperventilation.

Srinivasan J, Leventer RJ, Kornberg AJ, Dahl HH, Ryan MM. Srinivasan J, et al. Among authors: ryan mm. Pediatr Neurol. 2008 Apr;38(4):293-5. doi: 10.1016/j.pediatrneurol.2007.12.003. Pediatr Neurol. 2008. PMID: 18358413

6

Adolescent spinal muscular atrophy with calf hypertrophy and a deletion in the SMN gene.

Yiu EM, Ravat S, Ryan MM, Shield LK, Smith LJ, Kornberg AJ. Yiu EM, et al. Among authors: ryan mm. Muscle Nerve. 2008 Jul;38(1):930-2. doi: 10.1002/mus.21013. Muscle Nerve. 2008. PMID: 18508340

7

King-denborough syndrome caused by a novel mutation in the ryanodine receptor gene.

D'Arcy CE, Bjorksten A, Yiu EM, Bankier A, Gillies R, McLean CA, Shield LK, Ryan MM. D'Arcy CE, et al. Among authors: ryan mm. Neurology. 2008 Sep 2;71(10):776-7. doi: 10.1212/01.wnl.0000324929.33780.2f. Neurology. 2008. PMID: 18765655 No abstract available.

8

Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A.

Yiu EM, Burns J, Ryan MM, Ouvrier RA. Yiu EM, et al. Among authors: ryan mm. J Peripher Nerv Syst. 2008 Sep;13(3):236-41. doi: 10.1111/j.1529-8027.2008.00182.x. J Peripher Nerv Syst. 2008. PMID: 18844790

9

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: ryan mm. 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

10

Evolution of foot and ankle manifestations in children with CMT1A.

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

294 results

Search Page

Filters