Hepplewhite PD - Search Results

1

Cerebellar ataxia in patients with mitochondrial DNA disease: a molecular clinicopathological study.

Lax NZ, Hepplewhite PD, Reeve AK, Nesbitt V, McFarland R, Jaros E, Taylor RW, Turnbull DM. Lax NZ, et al. Among authors: hepplewhite pd. J Neuropathol Exp Neurol. 2012 Feb;71(2):148-61. doi: 10.1097/NEN.0b013e318244477d. J Neuropathol Exp Neurol. 2012. PMID: 22249460 Free PMC article.

2

The impact of pathogenic mitochondrial DNA mutations on substantia nigra neurons.

Reeve A, Meagher M, Lax N, Simcox E, Hepplewhite P, Jaros E, Turnbull D. Reeve A, et al. J Neurosci. 2013 Jun 26;33(26):10790-801. doi: 10.1523/JNEUROSCI.3525-12.2013. J Neurosci. 2013. PMID: 23804100 Free PMC article.

3

Sensory neuronopathy in patients harbouring recessive polymerase γ mutations.

Lax NZ, Whittaker RG, Hepplewhite PD, Reeve AK, Blakely EL, Jaros E, Ince PG, Taylor RW, Fawcett PR, Turnbull DM. Lax NZ, et al. Among authors: hepplewhite pd. Brain. 2012 Jan;135(Pt 1):62-71. doi: 10.1093/brain/awr326. Epub 2011 Dec 20. Brain. 2012. PMID: 22189570 Free PMC article.

4

Relationship between mitochondria and α-synuclein: a study of single substantia nigra neurons.

Reeve AK, Park TK, Jaros E, Campbell GR, Lax NZ, Hepplewhite PD, Krishnan KJ, Elson JL, Morris CM, McKeith IG, Turnbull DM. Reeve AK, et al. Among authors: hepplewhite pd. Arch Neurol. 2012 Mar;69(3):385-93. doi: 10.1001/archneurol.2011.2675. Arch Neurol. 2012. PMID: 22410447

5

Microangiopathy in the cerebellum of patients with mitochondrial DNA disease.

Lax NZ, Pienaar IS, Reeve AK, Hepplewhite PD, Jaros E, Taylor RW, Kalaria RN, Turnbull DM. Lax NZ, et al. Among authors: hepplewhite pd. Brain. 2012 Jun;135(Pt 6):1736-50. doi: 10.1093/brain/aws110. Epub 2012 May 9. Brain. 2012. PMID: 22577219 Free PMC article.

6

Quantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue.

Grünewald A, Lax NZ, Rocha MC, Reeve AK, Hepplewhite PD, Rygiel KA, Taylor RW, Turnbull DM. Grünewald A, et al. Among authors: hepplewhite pd. J Neurosci Methods. 2014 Jul 30;232(100):143-9. doi: 10.1016/j.jneumeth.2014.05.026. Epub 2014 May 29. J Neurosci Methods. 2014. PMID: 24880043 Free PMC article.

7

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

Lax NZ, Grady J, Laude A, Chan F, Hepplewhite PD, Gorman G, Whittaker RG, Ng Y, Cunningham MO, Turnbull DM. Lax NZ, et al. Among authors: hepplewhite pd. Neuropathol Appl Neurobiol. 2016 Feb;42(2):180-93. doi: 10.1111/nan.12238. Epub 2015 May 30. Neuropathol Appl Neurobiol. 2016. PMID: 25786813 Free PMC article.

8

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.

Ng YS, Lax NZ, Maddison P, Alston CL, Blakely EL, Hepplewhite PD, Riordan G, Meldau S, Chinnery PF, Pierre G, Chronopoulou E, Du A, Hughes I, Morris AA, Kamakari S, Chrousos G, Rodenburg RJ, Saris CGJ, Feeney C, Hardy SA, Sakakibara T, Sudo A, Okazaki Y, Murayama K, Mundy H, Hanna MG, Ohtake A, Schaefer AM, Champion MP, Turnbull DM, Taylor RW, Pitceathly RDS, McFarland R, Gorman GS. Ng YS, et al. Among authors: hepplewhite pd. EBioMedicine. 2018 Apr;30:86-93. doi: 10.1016/j.ebiom.2018.02.010. Epub 2018 Feb 24. EBioMedicine. 2018. PMID: 29506874 Free PMC article.

9

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

Reeve AK, Grady JP, Cosgrave EM, Bennison E, Chen C, Hepplewhite PD, Morris CM. Reeve AK, et al. Among authors: hepplewhite pd. NPJ Parkinsons Dis. 2018 Mar 26;4:9. doi: 10.1038/s41531-018-0044-6. eCollection 2018. NPJ Parkinsons Dis. 2018. PMID: 29872690 Free PMC article.

10

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

Grünewald A, Rygiel KA, Hepplewhite PD, Morris CM, Picard M, Turnbull DM. Grünewald A, et al. Among authors: hepplewhite pd. Ann Neurol. 2016 Mar;79(3):366-78. doi: 10.1002/ana.24571. Epub 2016 Jan 28. Ann Neurol. 2016. PMID: 26605748 Free PMC article.

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