Relaxed replication of mtDNA: A model with implications for the expression of disease.

od Chinnery, P F, Samuels, D C
Wydane 1999

Next generation sequencing for neurological diseases: New hope or new hype?

od Keogh, M.J., Chinnery, P.F.
Wydane 2013

The inheritance of pathogenic mitochondrial DNA mutations

od Cree, L.M., Samuels, D.C., Chinnery, P.F.
Wydane 2009

An under-recognised cause of spastic paraparesis in middle-aged women

od Bargiela, D, Eglon, G, Horvath, R, Chinnery, P F
Wydane 2013

Mitochondrial DNA mutations and pathogenicity.

od Chinnery, P F, Turnbull, D M, Howell, N, Andrews, R M
Wydane 1998

Genetic counseling and prenatal diagnosis for mtDNA disease.

od Chinnery, P F, Howell, N, Lightowlers, R N, Turnbull, D M
Wydane 1998

Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31

od Fisher, K. M., Chinnery, P. F., Baker, S. N., Baker, M. R.
Wydane 2013

Treatment strategies for inherited optic neuropathies: past, present and future

od Yu-Wai-Man, P, Votruba, M, Moore, A T, Chinnery, P F
Wydane 2014

Random Intracellular Drift Explains the Clonal Expansion of Mitochondrial DNA Mutations with Age

od Elson, J. L., Samuels, D. C., Turnbull, D. M., Chinnery, P. F.
Wydane 2001

Inherited mitochondrial optic neuropathies

od Yu-Wai-Man, P, Griffiths, P G, Hudson, G, Chinnery, P F
Wydane 2009

Psychophysical Evaluation of Cochlear Hair Cell Damage Due to the A3243G Mitochondrial DNA Mutation

od Griffiths, T. D., Blakemore, S., Elliott, C., Moore, B. C. J., Chinnery, P. F.
Wydane 2001

Eye movement recordings to investigate a supranuclear component in chronic progressive external ophthalmoplegia: a cross-sectional study

od Ritchie, A E, Griffiths, P G, Chinnery, P F, Davidson, A W
Wydane 2010

Random Genetic Drift Determines the Level of Mutant mtDNA in Human Primary Oocytes

od Brown, D. T., Samuels, D. C., Michael, E. M., Turnbull, D. M., Chinnery, P. F.
Wydane 2001

Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations

od Yu-Wai-Man, P, Bailie, M, Atawan, A, Chinnery, P F, Griffiths, P G
Wydane 2011

The minimum prevalence of CADASIL in northeast England

od Narayan, S.K., Gorman, G., Kalaria, R.N., Ford, G.A., Chinnery, P.F.
Wydane 2012

Management of parkinsonism and psychotic depression in a case of acute intermittent porphyria.

od Chinnery, P F, Cartlidge, N E, Burn, D J, Cleland, P G, McKeith, I
Wydane 1997

Fulminant encephalopathy due to the catastrophic primary antiphospholipid syndrome.

od Chinnery, P F, Shaw, P J, Ince, P G, Jackson, G H, Bishop, R I
Wydane 1997

Point Mutations of the mtDNA Control Region in Normal and Neurodegenerative Human Brains

od Chinnery, P. F., Taylor, G. A., Howell, N., Brown, D. T., Parsons, T. J., Turnbull, D. M.
Wydane 2001

The role of mitochondrial haplogroups in primary open angle glaucoma

od Andrews, R, Ressiniotis, T, Turnbull, D M, Birch, M, Keers, S, Chinnery, P F, Griffiths, P G
Wydane 2006

Progressive Brain Iron Accumulation in Neuroferritinopathy Measured by the Thalamic T2* Relaxation Rate

od McNeill, A., Gorman, G., Khan, A., Horvath, R., Blamire, A.M., Chinnery, P.F.
Wydane 2012