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Browsing publications by Dr James Miller

Newcastle AuthorsTitleYearFull text
Dr James Miller
Rituximab for myasthenia gravis2025
Dr James Miller
Electrodiagnostic subtyping in Guillain–Barré syndrome patients in the International Guillain–Barré Outcome Study2024
Dr James Miller
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease2024
Dr James Miller
CSF Findings in Relation to Clinical Characteristics, Subtype, and Disease Course in Patients With Guillain-Barré Syndrome2023
Dr James Miller
Rituximab for myasthenia gravis2023
Dr James Miller
Two emerging phenotypes of atypical inclusion body myositis: illustrative cases2023
Dr James Miller
An International Perspective on Preceding Infections in Guillain-Barré Syndrome: The IGOS-1000 Cohort2022
Dr Kirstie Anderson
Dr Naomi Warren
Dr Duddy Duddy
Dr James Miller
Delivering an advice and guidance service in neurology2022
Kundan Iqbal
Dr James Miller
Dr Horn Lai
Dr Ben Thompson
High median nerve lesion secondary to severe giant cell arteritis2022
Dr James Miller
Predicting Outcome in Guillain-Barré Syndrome International Validation of the Modified Erasmus GBS Outcome Score2022
Jane Newman
Dr James Miller
Professor Djordje Jakovljevic
Professor Grainne Gorman
Emeritus Professor Doug Turnbull
Interventions for promoting physical activity in people with neuromuscular disease2021
Dr James Miller
Long-term strength and functional status in inclusion body myositis and identification of trajectory subgroups2020
Dr Katherine Johnson
Dr Ana Topf
Dr Marta Bertoli
Lauren Charlotte Phillips Phillips
Dr James Miller
et al.
Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population2019
Dr Bridget Griffiths
Dr James Miller
Increasing incidence of adult idiopathic inflammatory myopathies in the City of Salford, UK: A 10-year epidemiological study2018
Dr Boglárka Bánsági
Professor Mark Baker
Matt Jennings
Professor Roger Whittaker
Dr Jennifer Duff
et al.
Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo PTEN mutation2018
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