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

by Chinnery, Patrick F
Published 2015

Diagnosis and treatment of mitochondrial myopathies

by Pfeffer, Gerald, Chinnery, Patrick F.
Published 2013

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

by Pfeffer, Gerald, Chinnery, Patrick F.
Published 2014

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

by Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Published 2011

Reply: Sensorineural hearing loss in OPA1-linked disorders

by Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Published 2013

Mitochondrial dysfunction in aging: Much progress but many unresolved questions

by Payne, Brendan A.I., Chinnery, Patrick F.
Published 2015

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

by Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Published 2014

Reply: ‘Behr syndrome’ with OPA1 compound heterozygote mutations

by Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Published 2015

Disorders of the Optic Nerve in Mitochondrial Cytopathies: New Ideas on Pathogenesis and Therapeutic Targets

by Sitarz, Kamil S., Chinnery, Patrick F., Yu-Wai-Man, Patrick
Published 2012

A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondr...

by Lythgow, Kieren T., Hudson, Gavin, Andras, Peter, Chinnery, Patrick F.
Published 2011

Mitochondrial optic neuropathies – Disease mechanisms and therapeutic strategies

by Yu-Wai-Man, Patrick, Griffiths, Philip G., Chinnery, Patrick F.
Published 2011

Elevated serum fibroblast growth factor 21 levels correlate with immune recovery but not mitochondrial dysfunction in HIV infection

by Payne, Brendan AI, Price, David Ashley, Chinnery, Patrick F
Published 2013

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

by Samuels, David C., Wonnapinij, Passorn, Chinnery, Patrick F.
Published 2013

Use of stereotypical mutational motifs to define resolution limits for the ultra-deep resequencing of mitochondrial DNA

by Gardner, Kristian, Payne, Brendan AI, Horvath, Rita, Chinnery, Patrick F
Published 2015

A polymorphism at codon 31 of gene p21 is not associated with primary open angle glaucoma in Caucasians

by Ressiniotis, Thomas, Griffiths, Philip G, Keers, Sharon M, Chinnery, Patrick F, Birch, Michael
Published 2005

OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy

by Yu-Wai-Man, Patrick, Trenell, Michael I., Hollingsworth, Kieren G., Griffiths, Philip G., Chinnery, Patrick F.
Published 2011

Raised Intraocular Pressure as a Potential Risk Factor for Visual Loss in Leber Hereditary Optic Neuropathy

by Thouin, Anais, Griffiths, Philip G., Hudson, Gavin, Chinnery, Patrick F., Yu-Wai-Man, Patrick
Published 2013

Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations

by Pfeffer, Gerald, Burke, Ailbhe, Yu-Wai-Man, Patrick, Compston, D. Alastair S., Chinnery, Patrick F.
Published 2013

Visual and psychological morbidity among patients with autosomal dominant optic atrophy

by Bailie, Maura, Votruba, Marcela, Griffiths, Philip G, Chinnery, Patrick F, Yu-Wai-Man, Patrick
Published 2013

A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failure☆

by Pfeffer, Gerald, Sambuughin, Nyamkhishig, Olivé, Montse, Tyndel, Felix, Toro, Camilo, Goldfarb, Lev G., Chinnery, Patrick F.
Published 2014