One complex world of mitochondrial parkinsonism

por Chinnery, Patrick F.
Publicado 2013

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

por Chinnery, Patrick F
Publicado en EMBO Mol Med (2015)

Lord Walton of Detchant: There and Back Again

por Chinnery, Patrick F.
Publicado en J Neuromuscul Dis (2015)

Diagnosis and treatment of mitochondrial myopathies

por Pfeffer, Gerald, Chinnery, Patrick F.
Publicado 2013

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

por Pfeffer, Gerald, Chinnery, Patrick F.
Publicado 2014

Nuclear-mitochondrial proteins: too much to process?

por Horvath, Rita, Chinnery, Patrick F.
Publicado en Brain (2015)

De-fusing mitochondria defuses the mtDNA time-bomb

por Chinnery, Patrick F., Prudent, Julien
Publicado en Cell Res (2019)

How to spot mitochondrial disease in adults

por Keogh, Michael J, Chinnery, Patrick F
Publicado en Clin Med (Lond) (2013)

Oldies but Goldies mtDNA Population Variants and Neurodegenerative Diseases

por Chinnery, Patrick F., Gomez-Duran, Aurora
Publicado en Front Neurosci (2018)

AMACR mutations cause late-onset autosomal recessive cerebellar ataxia

por Dick, David, Horvath, Rita, Chinnery, Patrick F.
Publicado 2011

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

por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado 2011

Reply: Sensorineural hearing loss in OPA1-linked disorders

por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado 2013

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

por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado 2014

Reply: ‘Behr syndrome’ with OPA1 compound heterozygote mutations

por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado en Brain (2015)

Leber Hereditary Optic Neuropathy – Therapeutic Challenges and Early Promise

por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado en Taiwan J Ophthalmol (2011)

How can we treat mitochondrial encephalomyopathies? approaches to therapy

por Horvath, Rita, Gorman, Grainne, Chinnery, Patrick F.
Publicado en Neurotherapeutics (2008)

Mitochondrial dysfunction in aging: Much progress but many unresolved questions

por Payne, Brendan A.I., Chinnery, Patrick F.
Publicado en Biochim Biophys Acta (2015)

Dominant Optic Atrophy – Novel OPA1 Mutations and Revised Prevalence Estimates

por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado en Ophthalmology (2013)

The Distribution of Mitochondrial DNA Heteroplasmy Due to Random Genetic Drift

por Wonnapinij, Passorn, Chinnery, Patrick F., Samuels, David C.
Publicado 2008

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

por Wonnapinij, Passorn, Chinnery, Patrick F., Samuels, David C.
Publicado 2010