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M. James

Newcastle University · GB
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Area of research
Molecular Biology · Physiology
Research interest
Research interests include Medicine, Duchenne muscular dystrophy, Clinical trial, Limb-girdle muscular dystrophy, Internal medicine, and Clinical endpoint.
h-index
citations
1,076
works
13
NIH funding
primary concept
email

Recent publications

Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy
Neuromuscular Disorders 2024cited by 1position: middledoi
Efficacy and Safety of Vamorolone vs Placebo and Prednisone Among Boys With Duchenne Muscular Dystrophy
JAMA Neurology 2022cited by 124position: middledoi
Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy
Orphanet Journal of Rare Diseases 2022cited by 35position: middledoi
Cardiac and pulmonary findings in dysferlinopathy: A 3‐year, longitudinal study
Muscle & Nerve 2022cited by 21position: middledoi
Water T2 could predict functional decline in patients with dysferlinopathy
Journal of Cachexia Sarcopenia and Muscle 2022cited by 20position: middledoi
Functional outcome measures in young, steroid-naïve boys with Duchenne muscular dystrophy
Neuromuscular Disorders 2022cited by 9position: middledoi
Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same disease
Neuromuscular Disorders 2021cited by 64position: middledoi
Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale
Annals of Neurology 2021cited by 35position: middledoi
Consensus Guidelines for Improving Quality of Assessment and Training for Neuromuscular Diseases
Frontiers in Genetics 2021cited by 12position: middledoi
Performance of Upper Limb module for Duchenne muscular dystrophy
Developmental Medicine & Child Neurology 2019cited by 76position: middledoi
Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials
Journal of Neurology Neurosurgery & Psychiatry 2018cited by 116position: middledoi
Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
The Lancet 2017cited by 453position: middledoi
The Clinical Outcome Study for dysferlinopathy
Neurology Genetics 2016cited by 110position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Anna Mayhew · Newcastle University4 papers (2019–2024)Volker Straub · ZHAW Zurich University of Applied Sciences3 papers (2019–2024)Laura Rufibach · Seattle University2 papers (2022–2024) · 2 papers (2019–2021)Linda Lowes · The Ohio State University2 papers (2021–2024)Kristy Rose · Sydney Children’s Hospitals Network2 papers (2021–2024) · 2 papers (2022–2024)Tina Duong · Palo Alto University2 papers (2021–2024)Lindsay N. Alfano · The Ohio State University2 papers (2021–2024)Ian Wilson · Newcastle University1 papers (2022–2022)Emmanuelle Salort‐Campana · Ludwig-Maximilians-Universität München1 papers (2022–2022)Jerry R. Mendell · Nationwide Children's Hospital1 papers (2022–2022)Kate Bushby · Newcastle University1 papers (2022–2022) · 1 papers (2022–2022)Marika Pane · University of Padua1 papers (2019–2019)Luca Bello · University of Padua1 papers (2024–2024)Simone Thiele · Ludwig-Maximilians-Universität München1 papers (2024–2024) · 1 papers (2022–2022)Katrijn Klingels · KU Leuven1 papers (2019–2019)Jordi Díaz‐Manera · Universitat de Barcelona1 papers (2022–2022)
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