209583/Z/17/Z/WT_/Wellcome Trust/United Kingdom[Grants and Funding] - Search Results

Year	Number of Results
2018	5
2019	4
2020	11
2021	5
2022	6
2024	0

1

Guidelines on clinical presentation and management of nondystrophic myotonias.

Stunnenberg BC, LoRusso S, Arnold WD, Barohn RJ, Cannon SC, Fontaine B, Griggs RC, Hanna MG, Matthews E, Meola G, Sansone VA, Trivedi JR, van Engelen BGM, Vicart S, Statland JM. Stunnenberg BC, et al. Muscle Nerve. 2020 Oct;62(4):430-444. doi: 10.1002/mus.26887. Epub 2020 May 27. Muscle Nerve. 2020. PMID: 32270509 Free PMC article. Review.

2

Translating genetic and functional data into clinical practice: a series of 223 families with myotonia.

Suetterlin K, Matthews E, Sud R, McCall S, Fialho D, Burge J, Jayaseelan D, Haworth A, Sweeney MG, Kullmann DM, Schorge S, Hanna MG, Männikkö R. Suetterlin K, et al. Brain. 2022 Apr 18;145(2):607-620. doi: 10.1093/brain/awab344. Brain. 2022. PMID: 34529042 Free PMC article.

3

Gene variant effects across sodium channelopathies predict function and guide precision therapy.

Brunklaus A, Feng T, Brünger T, Perez-Palma E, Heyne H, Matthews E, Semsarian C, Symonds JD, Zuberi SM, Lal D, Schorge S. Brunklaus A, et al. Brain. 2022 Dec 19;145(12):4275-4286. doi: 10.1093/brain/awac006. Brain. 2022. PMID: 35037686 Free PMC article.

4

Skeletal Muscle Channelopathies.

Vivekanandam V, Munot P, Hanna MG, Matthews E. Vivekanandam V, et al. Neurol Clin. 2020 Aug;38(3):481-491. doi: 10.1016/j.ncl.2020.04.003. Neurol Clin. 2020. PMID: 32703462 Review.

5

Treatment Updates for Neuromuscular Channelopathies.

Jitpimolmard N, Matthews E, Fialho D. Jitpimolmard N, et al. Curr Treat Options Neurol. 2020;22(10):34. doi: 10.1007/s11940-020-00644-2. Epub 2020 Aug 22. Curr Treat Options Neurol. 2020. PMID: 32848354 Free PMC article. Review.

6

Improving genetic diagnostics of skeletal muscle channelopathies.

Vivekanandam V, Männikkö R, Matthews E, Hanna MG. Vivekanandam V, et al. Expert Rev Mol Diagn. 2020 Jul;20(7):725-736. doi: 10.1080/14737159.2020.1782195. Epub 2020 Jul 12. Expert Rev Mol Diagn. 2020. PMID: 32657178 Review.

7

Skeletal muscle channelopathies: a guide to diagnosis and management.

Matthews E, Holmes S, Fialho D. Matthews E, et al. Pract Neurol. 2021 Jun;21(3):196-204. doi: 10.1136/practneurol-2020-002576. Epub 2021 Feb 9. Pract Neurol. 2021. PMID: 33563766 Review.

8

Muscle and brain sodium channelopathies: genetic causes, clinical phenotypes, and management approaches.

Matthews E, Balestrini S, Sisodiya SM, Hanna MG. Matthews E, et al. Lancet Child Adolesc Health. 2020 Jul;4(7):536-547. doi: 10.1016/S2352-4642(19)30425-0. Epub 2020 Mar 3. Lancet Child Adolesc Health. 2020. PMID: 32142633 Review.

9

Editorial: New Insights in Skeletal Muscle Channelopathies - A Rapidly Expanding Field.

Maggi L, Matthews E, Desaphy JF. Maggi L, et al. Front Neurol. 2020 Dec 17;11:626772. doi: 10.3389/fneur.2020.626772. eCollection 2020. Front Neurol. 2020. PMID: 33391177 Free PMC article. No abstract available.

10

Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancy.

Silksmith B, Munot P, Starling L, Pujar S, Matthews E. Silksmith B, et al. Lancet Child Adolesc Health. 2022 Jul;6(7):495-508. doi: 10.1016/S2352-4642(22)00091-8. Epub 2022 May 5. Lancet Child Adolesc Health. 2022. PMID: 35525254 Review.

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