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The long exercise test as a functional marker of periodic paralysis

Muscle & nerve, 2022-05, Vol.65 (5), p.581-585

2022

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

Neurology. Clinical practice, 2021-02, Vol.11 (1), p.e40-e42

2021

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

JCSM rapid communications, 2021-07, Vol.4 (2), p.245-259

2021

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Hallmarks of ageing in human skeletal muscle and implications for understanding the pathophysiology of sarcopenia in women and men

Clinical science (1979), 2023-11, Vol.137 (22), p.1721-1751

2023

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Proprioception: where are we now? A commentary on clinical assessment, changes across the life course, functional implications and future interventions

Age and ageing, 2014-05, Vol.43 (3), p.313-318

2014

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Muscle MRI in periodic paralysis shows myopathy is common and correlates with intramuscular fat accumulation

Muscle & nerve, 2023-10, Vol.68 (4), p.439-450

2023

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

Brain (London, England : 1878), 2022-04, Vol.145 (2), p.607-620

2022

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Muscle channelopathies: recent advances in genetics, pathophysiology and therapy

Current opinion in neurology, 2014-10, Vol.27 (5), p.583-590

2014

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

JAMA neurology, 2015-12, Vol.72 (12), p.1531

2015

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

Clinical neurophysiology, 2020-04, Vol.131 (4), p.816-827

2020

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Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy

Brain (London, England : 1878), 2016-03, Vol.139 (Pt 3), p.674-691

2016

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Diagnosis and management of headache

British journal of hospital medicine (London, England : 2005), 2014-12, Vol.75 (12), p.C178-C182

2014

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Atypical periodic paralysis and myalgia: A novel RYR1 phenotype

Neurology, 2018-01, Vol.90 (5), p.e412

2018

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Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation

Scientific reports, 2019-11, Vol.9 (1), p.17560-11, Article 17560

2019

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Understanding the Pathophysiology of Skeletal Muscle Channelopathies

Suetterlin, Karen Joan

2021

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Inherited myotonias

Handbook of Clinical Neurology, 2024, Vol.203, p.25-38

2024

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Mexiletine (NaMuscla) for the treatment of myotonia in non-dystrophic myotonic disorders

Expert opinion on orphan drugs, 2020-03, Vol.8 (2-3), p.43-49

2020

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Andersen-Tawil Syndrome Presenting with Complete Heart Block

Journal of neuromuscular diseases, 2021-01, Vol.8 (1), p.151-154

2021

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When is ‘idiopathic intracranial hypertension’ no longer idiopathic?

Practical neurology, 2014-04, Vol.14 (2), p.102-106

2014

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Muscle channelopathies

International Neurology, 2016, p.482-484

2016

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

Neurology. Clinical practice, 2021, Vol.11 (1), p.e40-e42

2021

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Wound Fluid from Breast Cancer Patients Undergoing Intraoperative Radiotherapy Exhibits an Altered Cytokine Profile and Impairs Mesenchymal Stromal Cell Function

Cancers, 2021-04, Vol.13 (9), p.2140

2021

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Intraoperative radiotherapy for breast cancer treatment efficiently targets the tumor bed preventing breast adipose stromal cell outgrowth

Strahlentherapie und Onkologie, 2020-04, Vol.196 (4), p.398-404

2020

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Application of intervention mapping in cybersecurity education design

Frontiers in education (Lausanne), 2022-11, Vol.7

2022

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The long exercise test as a functional marker of periodic paralysis

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

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

Hallmarks of ageing in human skeletal muscle and implications for understanding the pathophysiology of sarcopenia in women and men

Proprioception: where are we now? A commentary on clinical assessment, changes across the life course, functional implications and future interventions

Muscle MRI in periodic paralysis shows myopathy is common and correlates with intramuscular fat accumulation

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

Muscle channelopathies: recent advances in genetics, pathophysiology and therapy

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

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

Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy

Diagnosis and management of headache

Atypical periodic paralysis and myalgia: A novel RYR1 phenotype

Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation

Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients

Understanding the Pathophysiology of Skeletal Muscle Channelopathies

Inherited myotonias

Mexiletine (NaMuscla) for the treatment of myotonia in non-dystrophic myotonic disorders

Andersen-Tawil Syndrome Presenting with Complete Heart Block

When is ‘idiopathic intracranial hypertension’ no longer idiopathic?

Muscle channelopathies

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

Wound Fluid from Breast Cancer Patients Undergoing Intraoperative Radiotherapy Exhibits an Altered Cytokine Profile and Impairs Mesenchymal Stromal Cell Function

Intraoperative radiotherapy for breast cancer treatment efficiently targets the tumor bed preventing breast adipose stromal cell outgrowth

Application of intervention mapping in cybersecurity education design

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