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Mitochondrial dysfunction within the synapses of substantia nigra neurons in Parkinson's disease.
Published in:
NPJ Parkinson's Disease, 2018, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41531-018-0044-6
By:
- Reeve, Amy K.;
- Grady, John P.;
- Cosgrave, Eve M.;
- Bennison, Emma;
- Chen, Chun;
- Hepplewhite, Philippa D.;
- Morris, Christopher M.
Publication type:
Article
Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease.
Published in:
Neuropathology & Applied Neurobiology, 2016, v. 42, n. 2, p. 180, doi. 10.1111/nan.12238
By:
- 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.
Publication type:
Article
Microangiopathy in the cerebellum of patients with mitochondrial DNA disease.
Published in:
Brain: A Journal of Neurology, 2012, v. 135, n. 6, p. 1736, doi. 10.1093/brain/aws110
By:
- Lax, Nichola Z.;
- Pienaar, Ilse S.;
- Reeve, Amy K.;
- Hepplewhite, Philippa D.;
- Jaros, Evelyn;
- Taylor, Robert W.;
- Kalaria, Raj N.;
- Turnbull, Doug M.
Publication type:
Article
Sensory neuronopathy in patients harbouring recessive polymerase γ mutations.
Published in:
Brain: A Journal of Neurology, 2012, v. 135, n. 1, p. 62, doi. 10.1093/brain/awr326
By:
- Lax, Nichola Z.;
- Whittaker, Roger G.;
- Hepplewhite, Philippa D.;
- Reeve, Amy K.;
- Blakely, Emma L.;
- Jaros, Evelyn;
- Ince, Paul G.;
- Taylor, Robert W.;
- Fawcett, Peter R. W.;
- Turnbull, Doug M.
Publication type:
Article
Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.
Published in:
2016
By:
- Grünewald, Anne;
- Rygiel, Karolina A.;
- Hepplewhite, Philippa D.;
- Morris, Christopher M.;
- Picard, Martin;
- Turnbull, Doug M.;
- Grünewald, Anne
Publication type:
journal article

Found: 5

Mitochondrial dysfunction within the synapses of substantia nigra neurons in Parkinson's disease.

Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease.

Microangiopathy in the cerebellum of patients with mitochondrial DNA disease.

Sensory neuronopathy in patients harbouring recessive polymerase γ mutations.

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.