Suetterlin K - Search Results

1

Atypical periodic paralysis and myalgia: A novel RYR1 phenotype.

Matthews E, Neuwirth C, Jaffer F, Scalco RS, Fialho D, Parton M, Raja Rayan D, Suetterlin K, Sud R, Spiegel R, Mein R, Houlden H, Schaefer A, Healy E, Palace J, Quinlivan R, Treves S, Holton JL, Jungbluth H, Hanna MG. Matthews E, et al. Among authors: suetterlin k. Neurology. 2018 Jan 30;90(5):e412-e418. doi: 10.1212/WNL.0000000000004894. Epub 2018 Jan 3. Neurology. 2018. PMID: 29298851 Free PMC article.

2

The long exercise test as a functional marker of periodic paralysis.

Ribeiro A, Suetterlin KJ, Skorupinska I, Tan SV, Morrow JM, Matthews E, Hanna MG, Fialho D. Ribeiro A, et al. Among authors: suetterlin kj. Muscle Nerve. 2022 May;65(5):581-585. doi: 10.1002/mus.27465. Epub 2021 Dec 6. Muscle Nerve. 2022. PMID: 34817893 Free PMC article.

3

Ageing contributes to phenotype transition in a mouse model of periodic paralysis.

Suetterlin KJ, Tan SV, Mannikko R, Phadke R, Orford M, Eaton S, Sayer AA, Grounds MD, Matthews E, Greensmith L, Hanna MG. Suetterlin KJ, et al. JCSM Rapid Commun. 2021 Jul-Dec;4(2):245-259. doi: 10.1002/rco2.41. Epub 2021 May 5. JCSM Rapid Commun. 2021. PMID: 35174322 Free PMC article.

4

Long-term Safety and Efficacy of Mexiletine for Patients With Skeletal Muscle Channelopathies.

Suetterlin KJ, Bugiardini E, Kaski JP, Morrow JM, Matthews E, Hanna MG, Fialho D. Suetterlin KJ, et al. JAMA Neurol. 2015 Dec;72(12):1531-3. doi: 10.1001/jamaneurol.2015.2338. JAMA Neurol. 2015. PMID: 26658970 No abstract available.

5

Muscle channelopathies: recent advances in genetics, pathophysiology and therapy.

Suetterlin K, Männikkö R, Hanna MG. Suetterlin K, et al. Curr Opin Neurol. 2014 Oct;27(5):583-90. doi: 10.1097/WCO.0000000000000127. Curr Opin Neurol. 2014. PMID: 25188014 Review.

6

In vivo assessment of interictal sarcolemmal membrane properties in hypokalaemic and hyperkalaemic periodic paralysis.

Tan SV, Suetterlin K, Männikkö R, Matthews E, Hanna MG, Bostock H. Tan SV, et al. Among authors: suetterlin k. Clin Neurophysiol. 2020 Apr;131(4):816-827. doi: 10.1016/j.clinph.2019.12.414. Epub 2020 Jan 27. Clin Neurophysiol. 2020. PMID: 32066100

7

Andersen-Tawil Syndrome Presenting with Complete Heart Block.

Suetterlin K, Männikkö R, Flossmann E, Sud R, Fialho D, Vivekanandam V, James N, Gossios TD, Hanna MG, Savvatis K, Matthews E. Suetterlin K, et al. J Neuromuscul Dis. 2021;8(1):151-154. doi: 10.3233/JND-200572. J Neuromuscul Dis. 2021. PMID: 33074188

8

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.

9

Annual Renal Ultrasound May Prevent Acute Presentation With Acetazolamide-Associated Urolithiasis.

Suetterlin KJ, Vivekanandam V, James N, Sud R, Holmes S, Fialho D, Hanna MG, Matthews EL. Suetterlin KJ, et al. Neurol Clin Pract. 2021 Feb;11(1):e40-e42. doi: 10.1212/CPJ.0000000000000761. Neurol Clin Pract. 2021. PMID: 33968492 Free PMC article. No abstract available.

10

Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations.

Sun J, Luo S, Suetterlin KJ, Song J, Huang J, Zhu W, Xi J, Zhou L, Lu J, Lu J, Zhao C, Hanna MG, Männikkö R, Matthews E, Qiao K. Sun J, et al. Among authors: suetterlin kj. Neuromuscul Disord. 2021 Sep;31(9):829-838. doi: 10.1016/j.nmd.2021.03.014. Epub 2021 Apr 15. Neuromuscul Disord. 2021. PMID: 33965302

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