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Browsing publications by Dr Roger Whittaker

Newcastle AuthorsTitleYearFull text
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
Dr 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
Linda Heskamp
Dr Ian Schofield
Dr Roger Whittaker
Professor Andrew Blamire
et al.
Motor Unit Magnetic Resonance Imaging (MU-MRI) to determine the Morphology of Human Motor Units2019
Dr Grace McMacken
Dr Sally Spendiff
Dr 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
Dr 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
Dr Veronika Boczonadi
Dr Monika Olahova
Dr Boglarka Bansagi
Dr Andreas Roos
Dr Vankateswara Ramesh
et al.
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease2018
Dr Boglárka Bánsági
Dr Mark Baker
Matt Jennings
Dr Roger Whittaker
Dr Jennifer Duff
et al.
Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo PTEN mutation2018
Dr Grace McMacken
Daniel Cox
Dr Andreas Roos
Dr Roger Whittaker
Professor Hanns Lochmuller
et al.
The beta-adrenergic agonist salbutamol modulates neuromuscular junction formation in zebrafish models of human myasthenic syndromes2018
Professor Hanns Lochmuller
Dr Roger Whittaker
Professor Rita Horvath
Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome2017
Michael White
Dr Roger Whittaker
Dr Carolina Gandara de Souza
Dr Elizabeth Stoll
A Guide to Approaching Regulatory Considerations for Lentiviral-Mediated Gene Therapies2017
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