Author/Creator: Turnbull, Doug M. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Turnbull, Doug M.

1. Adult‐onset myoclonus ataxia associated with the mitochondrial m.8993T>C "NARP" mutation. Issue 10 (12th August 2015)

Authors:: Martikainen, Mika H.; Gorman, Grainne S.; Goldsmith, Paul; Burn, David J.; Turnbull, Doug M.; Schaefer, Andrew M.
Journal:: Movement disorders
Issue:: Volume 30:Issue 10(2015)
Page Start:: 1432
Record Type:: Journal Article
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2. Age‐associated mitochondrial complex I deficiency is linked to increased stem cell proliferation rates in the mouse colon. Issue 3 (24th February 2021)

Authors:: Stamp, Craig; Whitehall, Julia C.; Smith, Anna L. M.; Houghton, David; Bradshaw, Carla; Stoll, Elizabeth A.; Blain, Alasdair P.; Turnbull, Doug M.; Greaves, Laura C.
Journal:: Aging cell
Issue:: Volume 20:Issue 3(2021)
Page Start:: n/a
Record Type:: Journal Article
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3. Cognitive deficits in adult m.3243A>G‐ and m.8344A>G‐related mitochondrial disease: importance of correcting for baseline intellectual ability. Issue 5 (27th March 2019)

Authors:: Moore, Heather L.; Kelly, Thomas; Bright, Alexandra; Field, Robert H.; Schaefer, Andrew M.; Blain, Alasdair P.; Taylor, Robert W.; McFarland, Robert; Turnbull, Doug M.; Gorman, Gráinne S.
Journal:: Annals of clinical and translational neurology
Issue:: Volume 6:Issue 5(2019)
Page Start:: 826
Record Type:: Journal Article
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4. Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle. (15th April 2014)

Authors:: Campbell, Georgia; Krishnan, Kim J.; Deschauer, Marcus; Taylor, Robert W.; Turnbull, Doug M.
Journal:: Human molecular genetics
Issue:: Volume 23:Number 17(2014:Sep. 01)
Page Start:: 4612
Record Type:: Journal Article
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5. Dissecting the neuronal vulnerability underpinning Alpers' syndrome: a clinical and neuropathological study. (9th October 2018)

Authors:: Hayhurst, Hannah; Anagnostou, Maria‐Eleni; Bogle, Helen J.; Grady, John P.; Taylor, Robert W.; Bindoff, Laurence A.; McFarland, Robert; Turnbull, Doug M.; Lax, Nichola Z.
Journal:: Brain pathology
Issue:: Volume 29:Number 1(2019)
Page Start:: 97
Record Type:: Journal Article
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6. Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease. (30th May 2015)

Authors:: Lax, Nichola Z.; Grady, John; Laude, Alex; Chan, Felix; Hepplewhite, Philippa D.; Gorman, Grainne; Whittaker, Roger G.; Ng, Yi; Cunningham, Mark O.; Turnbull, Doug M.
Journal:: Neuropathology & applied neurobiology
Issue:: Volume 42:Number 2(2016)
Page Start:: 180
Record Type:: Journal Article
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7. Investigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial disease. (30th September 2015)

Authors:: Chrysostomou, Alexia; Grady, John P.; Laude, Alex; Taylor, Robert W.; Turnbull, Doug M.; Lax, Nichola Z.
Journal:: Neuropathology & applied neurobiology
Issue:: Volume 42:Number 5(2016)
Page Start:: 477
Record Type:: Journal Article
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8. Mitochondrial and inflammatory changes in sporadic inclusion body myositis. (April 2015)

Authors:: Rygiel, Karolina A.; Miller, James; Grady, John P.; Rocha, Mariana C.; Taylor, Robert W.; Turnbull, Doug M.
Journal:: Neuropathology & applied neurobiology
Issue:: Volume 41:Number 3(2015)
Page Start:: 288
Record Type:: Journal Article
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9. Mitochondrial DNA Depletion in Respiratory Chain–Deficient Parkinson Disease Neurons. Issue 3 (28th January 2016)

Authors:: Grünewald, Anne; Rygiel, Karolina A.; Hepplewhite, Philippa D.; Morris, Christopher M.; Picard, Martin; Turnbull, Doug M.
Journal:: Annals of neurology
Issue:: Volume 79:Issue 3(2016:Mar.)
Page Start:: 366
Record Type:: Journal Article
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10. Mitochondrial donation — hope for families with mitochondrial DNA disease. Issue 2 (23rd June 2020)

Authors:: Craven, Lyndsey; Murphy, Julie L.; Turnbull, Doug M.
Editors:: Reece, Richard
Journal:: Emerging topics in life sciences
Issue:: Volume 4:Issue 2(2020)
Page Start:: 151
Record Type:: Journal Article
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