受强制性开放获取政策约束的文章 - Karen Suetterlin了解详情
无法在其他位置公开访问的文章：1 篇
Muscle channelopathies: recent advances in genetics, pathophysiology and therapy
K Suetterlin, R Männikkö, MG Hanna
Current opinion in neurology 27 (5), 583-590, 2014
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council, National …
可在其他位置公开访问的文章：18 篇
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or ‘classical’ congenital myopathy
IT Zaharieva, MG Thor, EC Oates, C Van Karnebeek, G Hendson, E Blom, ...
Brain 139 (3), 674-691, 2016
强制性开放获取政策： National Health and Medical Research Council, Australia, Canadian Institutes …
Proprioception: where are we now? A commentary on clinical assessment, changes across the life course, functional implications and future interventions
KJ Suetterlin, AA Sayer
Age and ageing 43 (3), 313-318, 2014
强制性开放获取政策： UK Medical Research Council
Long-term safety and efficacy of mexiletine for patients with skeletal muscle channelopathies
KJ Suetterlin, E Bugiardini, JP Kaski, JM Morrow, E Matthews, MG Hanna, ...
JAMA neurology 72 (12), 1531-1533, 2015
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council, National …
Atypical periodic paralysis and myalgia: A novel RYR1 phenotype
E Matthews, C Neuwirth, F Jaffer, RS Scalco, D Fialho, M Parton, ...
Neurology 90 (5), e412-e418, 2018
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients
JP Molenaar, JI Verhoeven, RJ Rodenburg, EJ Kamsteeg, CE Erasmus, ...
Brain 143 (2), 452-466, 2020
强制性开放获取政策： UK Medical Research Council
Hallmarks of ageing in human skeletal muscle and implications for understanding the pathophysiology of sarcopenia in women and men
A Granic, K Suetterlin, T Shavlakadze, MD Grounds, AA Sayer
Clinical Science 137 (22), 1721-1751, 2023
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation
MG Thor, V Vivekanandam, M Sampedro-Castañeda, SV Tan, ...
Scientific reports 9 (1), 17560, 2019
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Translating genetic and functional data into clinical practice: a series of 223 families with myotonia
K Suetterlin, E Matthews, R Sud, S McCall, D Fialho, J Burge, ...
Brain 145 (2), 607-620, 2022
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
In vivo assessment of interictal sarcolemmal membrane properties in hypokalaemic and hyperkalaemic periodic paralysis
SV Tan, K Suetterlin, R Männikkö, E Matthews, MG Hanna, H Bostock
Clinical Neurophysiology 131 (4), 816-827, 2020
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council, National …
Mexiletine (NaMuscla) for the treatment of myotonia in non-dystrophic myotonic disorders
KJ Suetterlin, D Raja Rayan, E Matthews, MG Hanna
Expert Opinion on Orphan Drugs 8 (2-3), 43-49, 2020
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Ageing contributes to phenotype transition in a mouse model of periodic paralysis
KJ Suetterlin, SV Tan, R Mannikko, R Phadke, M Orford, S Eaton, ...
JCSM Rapid Communications 4 (2), 245-259, 2021
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
The long exercise test as a functional marker of periodic paralysis
A Ribeiro, KJ Suetterlin, I Skorupinska, SV Tan, JM Morrow, E Matthews, ...
Muscle & nerve 65 (5), 581-585, 2022
强制性开放获取政策： Canadian Institutes of Health Research, UK Medical Research Council …
Excitability properties of mouse and human skeletal muscle fibres compared by muscle velocity recovery cycles
KJ Suetterlin, R Männikkö, E Matthews, L Greensmith, MG Hanna, ...
Neuromuscular Disorders 32 (4), 347-357, 2022
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Muscle MRI in periodic paralysis shows myopathy is common and correlates with intramuscular fat accumulation
V Vivekanandam, K Suetterlin, E Matthews, J Thornton, D Jayaseelan, ...
Muscle & Nerve 68 (4), 439-450, 2023
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK
Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations
J Sun, S Luo, KJ Suetterlin, J Song, J Huang, W Zhu, J Xi, L Zhou, J Lu, ...
Neuromuscular Disorders 31 (9), 829-838, 2021
强制性开放获取政策： 国家自然科学基金委员会, UK Medical Research Council, National Institute for …
Annual renal ultrasound may prevent acute presentation with acetazolamide-associated urolithiasis
KJ Suetterlin, V Vivekanandam, N James, R Sud, S Holmes, D Fialho, ...
Neurology: Clinical Practice 11 (1), e40-e42, 2021
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council, National …
Andersen-tawil syndrome presenting with complete heart block
K Suetterlin, R Männikkö, E Flossmann, R Sud, D Fialho, ...
Journal of Neuromuscular Diseases 8 (1), 151-154, 2021
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Periodic paralysis across the life course: age-related phenotype transition and sarcopenia overlap
K Suetterlin, S Law, WD Arnold
Frontiers in Neurology 15, 1507485, 2024
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK
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