One complex world of mitochondrial parkinsonism

av Chinnery, Patrick F.
Publicerad 2013

Mitochondrial disease in adults: what's old and what's new?

av Chinnery, Patrick F
I publikationen EMBO Mol Med (2015)

Lord Walton of Detchant: There and Back Again

av Chinnery, Patrick F.
I publikationen J Neuromuscul Dis (2015)

Diagnosis and treatment of mitochondrial myopathies

av Pfeffer, Gerald, Chinnery, Patrick F.
Publicerad 2013

Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain

av Pfeffer, Gerald, Chinnery, Patrick F.
Publicerad 2014

Nuclear-mitochondrial proteins: too much to process?

av Horvath, Rita, Chinnery, Patrick F.
I publikationen Brain (2015)

De-fusing mitochondria defuses the mtDNA time-bomb

av Chinnery, Patrick F., Prudent, Julien
I publikationen Cell Res (2019)

How to spot mitochondrial disease in adults

av Keogh, Michael J, Chinnery, Patrick F
I publikationen Clin Med (Lond) (2013)

Oldies but Goldies mtDNA Population Variants and Neurodegenerative Diseases

av Chinnery, Patrick F., Gomez-Duran, Aurora
I publikationen Front Neurosci (2018)

AMACR mutations cause late-onset autosomal recessive cerebellar ataxia

av Dick, David, Horvath, Rita, Chinnery, Patrick F.
Publicerad 2011

Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation

av Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicerad 2011

Reply: Sensorineural hearing loss in OPA1-linked disorders

av Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicerad 2013

Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1

av Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicerad 2014

Reply: ‘Behr syndrome’ with OPA1 compound heterozygote mutations

av Yu-Wai-Man, Patrick, Chinnery, Patrick F.
I publikationen Brain (2015)

Leber Hereditary Optic Neuropathy – Therapeutic Challenges and Early Promise

av Yu-Wai-Man, Patrick, Chinnery, Patrick F.
I publikationen Taiwan J Ophthalmol (2011)

How can we treat mitochondrial encephalomyopathies? approaches to therapy

av Horvath, Rita, Gorman, Grainne, Chinnery, Patrick F.
I publikationen Neurotherapeutics (2008)

Mitochondrial dysfunction in aging: Much progress but many unresolved questions

av Payne, Brendan A.I., Chinnery, Patrick F.
I publikationen Biochim Biophys Acta (2015)

Dominant Optic Atrophy – Novel OPA1 Mutations and Revised Prevalence Estimates

av Yu-Wai-Man, Patrick, Chinnery, Patrick F.
I publikationen Ophthalmology (2013)

The Distribution of Mitochondrial DNA Heteroplasmy Due to Random Genetic Drift

av Wonnapinij, Passorn, Chinnery, Patrick F., Samuels, David C.
Publicerad 2008

Previous Estimates of Mitochondrial DNA Mutation Level Variance Did Not Account for Sampling Error: Comparing the mtDNA Genetic Bottleneck in Mice and Humans

av Wonnapinij, Passorn, Chinnery, Patrick F., Samuels, David C.
Publicerad 2010