Wraige E - Search Results

1

Long-term Natural History of Pediatric Dominant and Recessive RYR1-Related Myopathy.

Sarkozy A, Sa M, Ridout D, Fernandez-Garcia MA, Distefano MG, Main M, Sheehan J, Manzur AY, Munot P, Robb S, Wraige E, Quinlivan R, Scoto M, Baranello G, Gowda V, Mein R, Phadke R, Jungbluth H, Muntoni F. Sarkozy A, et al. Among authors: wraige e. Neurology. 2023 Oct 10;101(15):e1495-e1508. doi: 10.1212/WNL.0000000000207723. Epub 2023 Aug 29. Neurology. 2023. PMID: 37643885 Free PMC article.

2

Surgery for scoliosis in Duchenne muscular dystrophy.

Cheuk DK, Wong V, Wraige E, Baxter P, Cole A, N'Diaye T, Mayowe V. Cheuk DK, et al. Among authors: wraige e. Cochrane Database Syst Rev. 2007 Jan 24;(1):CD005375. doi: 10.1002/14651858.CD005375.pub2. Cochrane Database Syst Rev. 2007. Update in: Cochrane Database Syst Rev. 2013 Feb 28;(2):CD005375. doi: 10.1002/14651858.CD005375.pub3 PMID: 17253553 Updated. Review.

3

Neurocysticercosis masquerading as a cerebral infarct.

Wraige E, Graham J, Robb SA, Jan W. Wraige E, et al. J Child Neurol. 2003 Apr;18(4):298-300. doi: 10.1177/08830738030180040501. J Child Neurol. 2003. PMID: 12760435

4

Interfamilial phenotypic heterogeneity in SMARD1.

Joseph S, Robb SA, Mohammed S, Lillis S, Simonds A, Manzur AY, Walter S, Wraige E. Joseph S, et al. Among authors: wraige e. Neuromuscul Disord. 2009 Mar;19(3):193-5. doi: 10.1016/j.nmd.2008.11.013. Epub 2009 Jan 20. Neuromuscul Disord. 2009. PMID: 19157874

5

Charcot-Marie-Tooth (CMT) disease 1A with superimposed inflammatory polyneuropathy in children.

Desurkar A, Lin JP, Mills K, Al-Sarraj S, Jan W, Jungbluth H, Wraige E. Desurkar A, et al. Among authors: wraige e. Neuropediatrics. 2009 Apr;40(2):85-8. doi: 10.1055/s-0029-1237720. Epub 2009 Oct 6. Neuropediatrics. 2009. PMID: 19809938

6

Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectin.

Forrest K, Mellerio JE, Robb S, Dopping-Hepenstal PJ, McGrath JA, Liu L, Buk SJ, Al-Sarraj S, Wraige E, Jungbluth H. Forrest K, et al. Among authors: wraige e. Neuromuscul Disord. 2010 Nov;20(11):709-11. doi: 10.1016/j.nmd.2010.06.003. Epub 2010 Jul 10. Neuromuscul Disord. 2010. PMID: 20624679

7

Infantile onset myofibrillar myopathy due to recessive CRYAB mutations.

Forrest KM, Al-Sarraj S, Sewry C, Buk S, Tan SV, Pitt M, Durward A, McDougall M, Irving M, Hanna MG, Matthews E, Sarkozy A, Hudson J, Barresi R, Bushby K, Jungbluth H, Wraige E. Forrest KM, et al. Among authors: wraige e. Neuromuscul Disord. 2011 Jan;21(1):37-40. doi: 10.1016/j.nmd.2010.11.003. Epub 2010 Dec 3. Neuromuscul Disord. 2011. PMID: 21130652

8

Moving towards meaningful measurement: Rasch analysis of the North Star Ambulatory Assessment in Duchenne muscular dystrophy.

Mayhew A, Cano S, Scott E, Eagle M, Bushby K, Muntoni F; North Star Clinical Network for Paediatric Neuromuscular Disease. Mayhew A, et al. Dev Med Child Neurol. 2011 Jun;53(6):535-42. doi: 10.1111/j.1469-8749.2011.03939.x. Epub 2011 Mar 17. Dev Med Child Neurol. 2011. PMID: 21410696 Free article.

9

King-Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene.

Dowling JJ, Lillis S, Amburgey K, Zhou H, Al-Sarraj S, Buk SJ, Wraige E, Chow G, Abbs S, Leber S, Lachlan K, Baralle D, Taylor A, Sewry C, Muntoni F, Jungbluth H. Dowling JJ, et al. Among authors: wraige e. Neuromuscul Disord. 2011 Jun;21(6):420-7. doi: 10.1016/j.nmd.2011.03.006. Epub 2011 Apr 22. Neuromuscul Disord. 2011. PMID: 21514828

10

Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutations.

Klein A, Jungbluth H, Clement E, Lillis S, Abbs S, Munot P, Pane M, Wraige E, Schara U, Straub V, Mercuri E, Muntoni F. Klein A, et al. Among authors: wraige e. Arch Neurol. 2011 Sep;68(9):1171-9. doi: 10.1001/archneurol.2011.188. Arch Neurol. 2011. PMID: 21911697

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