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Why are some patients with Duchenne muscular dystrophy dying young: an analysis of causes of death in North East England

European journal of paediatric neurology, 2016-11, Vol.20 (6), p.904-909

2016

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Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging

European journal of neurology, 2020-12, Vol.27 (12), p.2604-2615

2020

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Survival patterns and cancer determinants in families with myotonic dystrophy type 1

European journal of neurology, 2019-01, Vol.26 (1), p.58-65

2019

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Adult North Star Network (ANSN): Consensus Guideline For The Standard Of Care Of Adults With Duchenne Muscular Dystrophy

Journal of neuromuscular diseases, 2021-01, Vol.8 (6), p.899-926

2021

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Intracortical excitability in patients with relapsing–remitting and secondary progressive multiple sclerosis

Journal of neurology, 2009-06, Vol.256 (6), p.933-938

2009

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Cautionary tale in Duchenne muscular dystrophy – Opioids in neuromuscular disorders

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S200-S200

2015

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Acute and chronic effects of ethanol on cortical excitability

Clinical neurophysiology, 2008-03, Vol.119 (3), p.667-674

2008

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Axial involvement as a prominent feature in SMPX-related distal myopathy

Neuromuscular disorders : NMD, 2024-06, Vol.39, p.3-4

2024

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Topiramate and cortical excitability in humans : a study with repetitive transcranial magnetic stimulation

Experimental brain research, 2006-10, Vol.174 (4), p.667-672

2006

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The 2.5 MeV neutron flux monitor for MAST

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2014-07, Vol.753, p.72-83

2014

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A Monte Carlo method for calculating the energy response of plastic scintillators to polarized photons below 100 keV

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2009-03, Vol.600 (3), p.609-617

2009

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Muscle magnetic resonance imaging in VCP-related multi-system proteinopathy (IBMPFD): is the clue in the “fat pockets”?

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S44-S44

2017

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Beam test of a prototype phoswich detector assembly for the PoGOLite astronomical soft gamma-ray polarimeter

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2007, Vol.570 (1), p.61-71

2007

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An audit on the reasons why patients failed to attend the Newcastle University Trust Hospitals’ Neuromuscular Clinics, at the John Walton Muscular Dystrophy Research Centre, and the actions taken

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S38-S39

2017

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Audit of unplanned hospital admissions for patients with neuromuscular disorders in the North East

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S38-S38

2017

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Case report of adult-onset Allgrove syndrome

Neurological sciences, 2007-12, Vol.28 (6), p.331-335

2007

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Measurement of the γ-ray energy resolution function of EJ301 liquid scintillator using a dual channel ADC

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2014-07, Vol.753, p.34-37

2014

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Telethonin gene mutations detected by next generation sequencing

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S15-S15

2017

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Respiratory involvement in Facioscapulohumeral Dystrophy

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S9-S9

2017

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Overview of morbidity, mortality and survival in Duchenne muscular dystrophy in the North East of England

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S301-S302

2015

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TH‐E‐217BCD‐06: Liquids for the Simulation of the X‐Ray Properties of Breast Tissue

Medical Physics, 2012-06, Vol.39 (6), p.4015-4015

2012

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Impact of three decades of improvements in standards of care on clinical outcomes in Duchenne muscular dystrophy

European journal of paediatric neurology, 2017-06, Vol.21, p.e235-e236

2017

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A novel STIM1 mutation at p.340 causes tubular aggregate myopathy with miosis without additional features of Stormorken syndrome

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S289-S289

2015

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133P Description of UK SMA cohorts since the introduction of disease modifying therapies

Neuromuscular disorders : NMD, 2024-10, Vol.43

2024

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206P A quality improvement proposal: improving care management of complex neuromuscular patients – establishing a neuromuscular complex care centre as part of the translational neuromuscular pathway

Neuromuscular disorders : NMD, 2024-10, Vol.43

2024

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Why are some patients with Duchenne muscular dystrophy dying young: an analysis of causes of death in North East England

Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging

Survival patterns and cancer determinants in families with myotonic dystrophy type 1

Adult North Star Network (ANSN): Consensus Guideline For The Standard Of Care Of Adults With Duchenne Muscular Dystrophy

Intracortical excitability in patients with relapsing–remitting and secondary progressive multiple sclerosis

Cautionary tale in Duchenne muscular dystrophy – Opioids in neuromuscular disorders

Acute and chronic effects of ethanol on cortical excitability

Axial involvement as a prominent feature in SMPX-related distal myopathy

Topiramate and cortical excitability in humans : a study with repetitive transcranial magnetic stimulation

The 2.5 MeV neutron flux monitor for MAST

A Monte Carlo method for calculating the energy response of plastic scintillators to polarized photons below 100 keV

Muscle magnetic resonance imaging in VCP-related multi-system proteinopathy (IBMPFD): is the clue in the “fat pockets”?

Beam test of a prototype phoswich detector assembly for the PoGOLite astronomical soft gamma-ray polarimeter

An audit on the reasons why patients failed to attend the Newcastle University Trust Hospitals’ Neuromuscular Clinics, at the John Walton Muscular Dystrophy Research Centre, and the actions taken

Audit of unplanned hospital admissions for patients with neuromuscular disorders in the North East

Case report of adult-onset Allgrove syndrome

Measurement of the γ-ray energy resolution function of EJ301 liquid scintillator using a dual channel ADC

Telethonin gene mutations detected by next generation sequencing

Respiratory involvement in Facioscapulohumeral Dystrophy

Overview of morbidity, mortality and survival in Duchenne muscular dystrophy in the North East of England

TH‐E‐217BCD‐06: Liquids for the Simulation of the X‐Ray Properties of Breast Tissue

Impact of three decades of improvements in standards of care on clinical outcomes in Duchenne muscular dystrophy

A novel STIM1 mutation at p.340 causes tubular aggregate myopathy with miosis without additional features of Stormorken syndrome

133P Description of UK SMA cohorts since the introduction of disease modifying therapies

206P A quality improvement proposal: improving care management of complex neuromuscular patients – establishing a neuromuscular complex care centre as part of the translational neuromuscular pathway

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