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Browsing publications by Dr Philip Nichols.

Newcastle AuthorsTitleYearFull text
Dr Vanessa Hogan
Dr Kathryn White
Emeritus Professor Doug Turnbull
Dr Philip Nichols
Increase in mitochondrial density within axons and supporting cells in response to demyelination in the Plp1 mouse model2009
Dr Kathryn White
Dr Vanessa Hogan
Dr Philip Nichols
Emeritus Professor Doug Turnbull
OPA1 Deficiency Associated with Increased Autophagy in Retinal Ganglion Cells in a Murine Model of Dominant Optic Atrophy2009
Dr Kathryn White
Dr Vanessa Hogan
Dr Philip Nichols
A missense mutation in the murine Opa3 gene models human Costeff syndrome2008
Dr Vanessa Hogan
Dr Kathleen White
Emeritus Professor Doug Turnbull
Dr Philip Nichols
Role of mitochondria in a mouse model of multiple sclerosis2008
Dr Karen Fisher
Dr Philip Nichols
Professor Mark Baker
Professor Stuart Baker
The effect of levetiracetam on cerebellar intention tremor in patients with multiple sclerosis2008
Dr Vanessa Hogan
Dr Kathleen White
Emeritus Professor David Bates
Emeritus Professor Doug Turnbull
Dr Philip Nichols
et al.
An increase in axonal mitochondrial density may play a role in axonal loss following myelin degeneration in the Plp1 mouse model of demyelination2007
Dr Vanessa Hogan
Dr Kathleen White
Emeritus Professor Doug Turnbull
Dr Philip Nichols
Axonal adaptation to demyelination in the Plp mouse2007
Dr Philip Nichols
Professor Tim Griffiths
Course and outcome of acute limbic encephalitis with negative voltage-gated potassium channel antibodies2007
Dr Kathryn White
Dr Philip Nichols
Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function2007
Dr Helen Andrews
Dr Kathryn White
Emeritus Professor David Bates
Emeritus Professor Doug Turnbull
Dr Philip Nichols
et al.
Increased axonal mitochondrial activity as an adaptation to myelin deficiency in the Shiverer mouse2006
Dr Helen Andrews
Dr Kathleen White
Christopher Thomson
Emeritus Professor David Bates
Emeritus Professor Doug Turnbull
et al.
A role for mitochondria in axonal loss in multiple sclerosis: studies in the Shiverer mouse model2005
Dr Philip Nichols
Dr Helen Andrews
Dr Kathleen White
Emeritus Professor David Bates
Emeritus Professor Doug Turnbull
et al.
A role for mitochondria in chronic axonal loss in multiple sclerosis: Studies at early and late time points in the shiverer mouse model2005
Dr Helen Andrews
Dr Kathleen White
Emeritus Professor David Bates
Emeritus Professor Doug Turnbull
Dr Philip Nichols
et al.
A role for mitochondria in chronic axonal loss in multiple sclerosis: studies at early and late time points in the shiverer mouse model2005
Dr Helen Andrews
Dr Kathleen White
Emeritus Professor David Bates
Emeritus Professor Doug Turnbull
Dr Philip Nichols
et al.
Mitochondria and axonal loss in multiple sclerosis: the missing link?2005
Dr Helen Andrews
Dr Kathleen White
Christopher Thomson
Emeritus Professor David Bates
Emeritus Professor Doug Turnbull
et al.
Mitochondria and axonal loss in multiple sclerosis: the shiverer mouse as a model of secondary progressive MS2005
Dr Helen Andrews
Dr Philip Nichols
Emeritus Professor David Bates
Emeritus Professor Doug Turnbull
Mitochondrial dysfunction plays a key role in progressive axonal loss in Multiple Sclerosis2005
Dr Martin Barron
Philip Griffiths
Emeritus Professor Doug Turnbull
Emeritus Professor David Bates
Dr Philip Nichols
et al.
The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head2004
Dr Martin Barron
Emeritus Professor Doug Turnbull
Emeritus Professor David Bates
Dr Philip Nichols
[abstract] Neuronal loss in Multiple Sclerosis: Role of Mitochondria in the Axonal response to Demyelination2003
Dr Philip Nichols
Dr Peter Newman
Progressive Multifocal Leucoencephalopathy (PML) complicating occult pulmonary sarcoidosis2001
Dr Philip Nichols
Wound botulism in drug addicts in the United Kingdom2001
Dr Philip Nichols
Mutation of the Acetylcholine Receptor ɛ-Subunit Promoter in Congenital Myasthenic Syndrome1999