| 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 | 115 | 2016 |
| 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 | 94 | 2014 |
| Muscle channelopathies: recent advances in genetics, pathophysiology and therapy K Suetterlin, R Männikkö, MG Hanna Current opinion in neurology 27 (5), 583-590, 2014 | 74 | 2014 |
| 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 | 57 | 2015 |
| International neurology RP Lisak, DD Truong, WM Carroll, R Bhidayasiri John Wiley & Sons, 2016 | 50 | 2016 |
| 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 | 45 | 2018 |
| 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 | 25 | 2020 |
| 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 | 18 | 2019 |
| 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 | 14 | 2022 |
| 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 | 13 | 2020 |
| 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 | 7 | 2023 |
| 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 | 6 | 2021 |
| 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 | 6 | 2020 |
| 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 | 5 | 2022 |
| 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 | 4 | 2021 |
| 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 | 4 | 2021 |
| 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 | 3 | 2022 |
| 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 | 3 | 2021 |
| When is ‘idiopathic intracranial hypertension’no longer idiopathic? K Suetterlin, N Borg, H Joy, JK Lovett, BCP Ghosh Practical Neurology 14 (2), 102-106, 2014 | 3 | 2014 |
| Diagnosis and management of headache K Suetterlin, C Turner British Journal of Hospital Medicine 75 (Sup12), C178-C182, 2014 | 2 | 2014 |
Hanna MichaelUCL Institute of Neurology在 ucl.ac.uk 的电子邮件经过验证
