Matthews E - Search Results

1

Fialho D, Griggs RC, Matthews E. Fialho D, et al. Among authors: matthews e. Handb Clin Neurol. 2018;148:505-520. doi: 10.1016/B978-0-444-64076-5.00032-6. Handb Clin Neurol. 2018. PMID: 29478596 Review.

2

Skeletal-muscle channelopathies: periodic paralysis and nondystrophic myotonias.

Ryan AM, Matthews E, Hanna MG. Ryan AM, et al. Among authors: matthews e. Curr Opin Neurol. 2007 Oct;20(5):558-63. doi: 10.1097/WCO.0b013e3282efc16c. Curr Opin Neurol. 2007. PMID: 17885445 Review.

3

What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealed.

Matthews E, Tan SV, Fialho D, Sweeney MG, Sud R, Haworth A, Stanley E, Cea G, Davis MB, Hanna MG. Matthews E, et al. Neurology. 2008 Jan 1;70(1):50-3. doi: 10.1212/01.wnl.0000287069.21162.94. Neurology. 2008. PMID: 18166706

4

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.

Matthews E, Labrum R, Sweeney MG, Sud R, Haworth A, Chinnery PF, Meola G, Schorge S, Kullmann DM, Davis MB, Hanna MG. Matthews E, et al. Neurology. 2009 May 5;72(18):1544-7. doi: 10.1212/01.wnl.0000342387.65477.46. Epub 2008 Dec 31. Neurology. 2009. PMID: 19118277 Free PMC article.

5

The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.

Matthews E, Fialho D, Tan SV, Venance SL, Cannon SC, Sternberg D, Fontaine B, Amato AA, Barohn RJ, Griggs RC, Hanna MG; CINCH Investigators. Matthews E, et al. Brain. 2010 Jan;133(Pt 1):9-22. doi: 10.1093/brain/awp294. Epub 2009 Nov 16. Brain. 2010. PMID: 19917643 Free PMC article. Review.

6

Muscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?

Matthews E, Hanna MG. Matthews E, et al. J Physiol. 2010 Jun 1;588(Pt 11):1879-86. doi: 10.1113/jphysiol.2009.186627. Epub 2010 Feb 1. J Physiol. 2010. PMID: 20123788 Free PMC article. Review.

7

Refined exercise testing can aid DNA-based diagnosis in muscle channelopathies.

Tan SV, Matthews E, Barber M, Burge JA, Rajakulendran S, Fialho D, Sud R, Haworth A, Koltzenburg M, Hanna MG. Tan SV, et al. Among authors: matthews e. Ann Neurol. 2011 Feb;69(2):328-40. doi: 10.1002/ana.22238. Ann Neurol. 2011. PMID: 21387378 Free PMC article.

8

An interactive voice response diary for patients with non-dystrophic myotonia.

Statland JM, Wang Y, Richesson R, Bundy B, Herbelin L, Gomes J, Trivedi J, Venance S, Amato A, Hanna M, Griggs R, Barohn RJ; Cinch Consortium. Statland JM, et al. Muscle Nerve. 2011 Jul;44(1):30-5. doi: 10.1002/mus.22007. Muscle Nerve. 2011. PMID: 21674518 Free PMC article.

9

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype.

Matthews E, Portaro S, Ke Q, Sud R, Haworth A, Davis MB, Griggs RC, Hanna MG. Matthews E, et al. Neurology. 2011 Nov 29;77(22):1960-4. doi: 10.1212/WNL.0b013e31823a0cb6. Epub 2011 Nov 16. Neurology. 2011. PMID: 22094484 Free PMC article.

10

A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1.

Raja Rayan DL, Haworth A, Sud R, Matthews E, Fialho D, Burge J, Portaro S, Schorge S, Tuin K, Lunt P, McEntagart M, Toscano A, Davis MB, Hanna MG. Raja Rayan DL, et al. Among authors: matthews e. Neurology. 2012 Jun 12;78(24):1953-8. doi: 10.1212/WNL.0b013e318259e19c. Epub 2012 May 30. Neurology. 2012. PMID: 22649220 Free PMC article.

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

709 results

Search Page