One complex world of mitochondrial parkinsonism

Por Chinnery, Patrick F.
Publicado em 2013

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

Por Chinnery, Patrick F
Publicado no EMBO Mol Med (2015)

Lord Walton of Detchant: There and Back Again

Por Chinnery, Patrick F.
Publicado no J Neuromuscul Dis (2015)

Diagnosis and treatment of mitochondrial myopathies

Por Pfeffer, Gerald, Chinnery, Patrick F.
Publicado em 2013

Mitochondrial genetics

Por Chinnery, Patrick Francis, Hudson, Gavin
Publicado em 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 em 2014

Nuclear-mitochondrial proteins: too much to process?

Por Horvath, Rita, Chinnery, Patrick F.
Publicado no Brain (2015)

AMACR mutations cause late-onset autosomal recessive cerebellar ataxia

Por Dick, David, Horvath, Rita, Chinnery, Patrick F.
Publicado em 2011

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

Por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado em 2011

Reply: Sensorineural hearing loss in OPA1-linked disorders

Por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado em 2013

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

Por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado em 2014

Reply: ‘Behr syndrome’ with OPA1 compound heterozygote mutations

Por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado no Brain (2015)

Leber Hereditary Optic Neuropathy – Therapeutic Challenges and Early Promise

Por Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Publicado no Taiwan J Ophthalmol (2011)

How can we treat mitochondrial encephalomyopathies? approaches to therapy

Por Horvath, Rita, Gorman, Grainne, Chinnery, Patrick F.
Publicado no Neurotherapeutics (2008)

Mitochondrial dysfunction in aging: Much progress but many unresolved questions

Por Payne, Brendan A.I., Chinnery, Patrick F.
Publicado no Biochim Biophys Acta (2015)

The Distribution of Mitochondrial DNA Heteroplasmy Due to Random Genetic Drift

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

Preventing the transmission of pathogenic mitochondrial DNA mutations: can we achieve long-term benefits from germ-line gene transfer?

Por Samuels, David C., Wonnapinij, Passorn, Chinnery, Patrick F.
Publicado em 2013

Selection against Pathogenic mtDNA Mutations in a Stem Cell Population Leads to the Loss of the 3243A→G Mutation in Blood

Por Rajasimha, Harsha Karur, Chinnery, Patrick F., Samuels, David C.
Publicado em 2008

Detecting new neurodegenerative disease genes: does phenotype accuracy limit the horizon?

Por Samuels, David C., Burn, David J., Chinnery, Patrick F.
Publicado em 2009