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Browsing publications by Professor Roger Whittaker

Newcastle AuthorsTitleYearFull text
Matt Birkbeck
Dr Linda Heskamp
Dr Ian Schofield
Professor Andrew Blamire
Professor Roger Whittaker
et al.
Non-invasive Imaging of Single Human Motor Units2020
Dr Emma Brunton
Dr Enrique Escobedo-Cousin
Dr Gaurav Gupta
Professor Roger Whittaker
Professor Anthony O'Neill
et al.
W:Ti flexible transversal electrode array for peripheral nerve stimulation: A feasibility study2020
Dr Veronika Boczonadi
Dr Monika Olahova
Dr Boglárka Bánsági
Dr Andreas Roos
Dr Vankateswara Ramesh
et al.
Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease (Genetics in Medicine, (2018), 20, 10, (1224-1235), 10.1038/gim.2017.251)2019
Professor Roger Whittaker
Dr Paola Porcari
Dr Luis Braz
Dr Ian Schofield
Professor Andrew Blamire
et al.
Functional MR imaging of human motor unit fasciculation in Amyotrophic Lateral Sclerosis2019
Matt Birkbeck
Dr Ian Schofield
Dr Linda Heskamp
Professor Roger Whittaker
Professor Andrew Blamire
et al.
Motor Unit Magnetic Resonance Imaging (MU-MRI) to Determine the Morphology and Distribution of Human Motor Units2019
Matt Birkbeck
Dr Linda Heskamp
Dr Ian Schofield
Professor Roger Whittaker
Professor Andrew Blamire
et al.
Motor Unit Magnetic Resonance Imaging (MU-MRI) to determine the Morphology of Human Motor Units2019
Dr Luis Braz
Dr Yi Ng
Dr Grainne Gorman
Professor Bobby McFarland
Professor Robert Taylor
et al.
Neuromuscular junction abnormalities in mitochondrial disease; an observational cohort study2019
Matt Birkbeck
Dr Linda Heskamp
Dr Ian Schofield
Professor Avan Sayer
Professor Andrew Blamire
et al.
Non-Invasive Imaging of Human Motor Units2019
Dr Grace McMacken
Dr Sally Spendiff
Professor Roger Whittaker
Emily O'Connor
Rachel Howarth
et al.
Salbutamol modifies the neuromuscular junction in a mouse model of ColQ myasthenic syndrome2019
Dr Grace McMacken
Professor Roger Whittaker
Dr Teresinha Evangelista
Professor Hanns Lochmuller
Congenital myasthenic syndrome with episodic apnoea: clinical, neurophysiological and genetic features in the long-term follow-up of 19 patients2018
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