Searching for nuclear-mitochondrial genesCHINNERY, Patrick F.Trends in genetics (Regular ed.). 2003, Vol 19, Num 2, pp 60-62, issn 0168-9525, 3 p.Article

One complex world of mitochondrial parkinsonismCHINNERY, Patrick F.Brain. 2013, Vol 136, pp 2336-2339, issn 0006-8950, 4 p., 8Article

Could it be mitochondrial? When and how to investigateCHINNERY, Patrick F.Practical neurology (Print). 2006, Vol 6, Num 2, pp 90-101, issn 1474-7758, 12 p.Article

Mitochondrial DNA polymerase-γ and human diseaseHUDSON, Gavin; CHINNERY, Patrick F.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R244-R252, NS2Article

Existing and emerging mitochondrial-targeting therapies for altering Parkinson's disease severity and progressionPIENAAR, Ilse S; CHINNERY, Patrick F.Pharmacology & therapeutics (Oxford). 2013, Vol 137, Num 1, pp 1-21, issn 0163-7258, 21 p.Article

The Distribution of Mitochondrial DNA Heteroplasmy Due to Random Genetic DriftWONNAPINIJ, Passorn; CHINNERY, Patrick F; SAMUELS, David C et al.American journal of human genetics. 2008, Vol 83, Num 5, pp 582-593, issn 0002-9297, 12 p.Article

How to spot mitochondrial disease in adultsKEOGH, Michael J; CHINNERY, Patrick F.Clinical medicine. 2013, Vol 13, Num 1, pp 87-92, issn 1470-2118, 6 p.Article

Selection against Pathogenic mtDNA Mutations in a Stem Cell Population Leads to the Loss of the 3243A→G Mutation in BloodKARUR RAJASIMHA, Harsha; CHINNERY, Patrick F; SAMUELS, David C et al.American journal of human genetics. 2008, Vol 82, Num 2, pp 333-343, issn 0002-9297, 11 p.Article

Detecting new neurodegenerative disease genes: does phenotype accuracy limit the horizon?SAMUELS, David C; BURN, David J; CHINNERY, Patrick F et al.Trends in genetics (Regular ed.). 2009, Vol 25, Num 11, pp 486-488, issn 0168-9525, 3 p.Article

Two direct repeats cause most human mtDNA deletionsSAMUELS, David C; SCHON, Eric A; CHINNERY, Patrick F et al.Trends in genetics (Regular ed.). 2004, Vol 20, Num 9, pp 393-398, issn 0168-9525, 6 p.Article

An Investigation of Mitochondrial Haplogroups in AutismKENT, Lindsey; GALLAGHER, Louise; ELLIOTT, Hannah R et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 6, pp 987-989, issn 1552-4841, 3 p.Article

Dramatic Response of Facial Stereotype/Tic to Tetrabenazine in the First Reported Cases of Neuroferritinopathy in the United StatesONDO, William G; ADAM, Octavian R; JANKOVIC, Joseph et al.Movement disorders. 2010, Vol 25, Num 14, pp 2470-2472, issn 0885-3185, 3 p.Article

Progressive depletion of mtDNA in mitochondrial myopathyDURHAM, Steve E; BROWN, Denise T; TURNBULL, Douglass M et al.Neurology. 2006, Vol 67, Num 3, pp 502-504, issn 0028-3878, 3 p.Article

The role of apolipoprotein E gene polymorphisms in primary open-angle glaucomaRESSINIOTIS, Thomas; GRIFFITHS, Philip G; BIRCH, Michael et al.Archives of ophthalmology (1960). 2004, Vol 122, Num 2, pp 258-261, issn 0003-9950, 4 p.Article

Evolutionary diversification of mitochondrial proteomes: implications for human diseaseRICHLY, Erik; CHINNERY, Patrick F; LEISTER, Dario et al.Trends in genetics (Regular ed.). 2003, Vol 19, Num 7, pp 356-362, issn 0168-9525, 7 p.Article

Late-onset axial jerky dystonia due to the DYT1 deletionCHINNERY, Patrick F; READING, Paul J; MCCARTHY, Emma L et al.Movement disorders. 2002, Vol 17, Num 1, pp 196-198, issn 0885-3185Article

Epidemiology and treatment of mitochondrial disordersCHINNERY, Patrick F; TURNBULL, Douglass M.American journal of medical genetics. 2001, Vol 106, Num 1, pp 94-101, issn 0148-7299Article

mtDNA mutations and common neurodegenerative disordersHOWELL, Neil; ELSON, Joanna L; CHINNERY, Patrick F et al.Trends in genetics (Regular ed.). 2005, Vol 21, Num 11, pp 583-586, issn 0168-9525, 4 p.Article

Limbic encephalitis: Not a picture to forgetCHINNERY, Patrick F; COTTRELL, David A; BIRCHALL, Daniel et al.Neurology. 2004, Vol 62, Num 6, issn 0028-3878, p. 1019Article

Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: Is there a common mechanism?CHINNERY, Patrick F; SAMUELS, David C; ELSON, Joanna et al.Lancet (British edition). 2002, Vol 360, Num 9342, pp 1323-1325, issn 0140-6736Article

Leber hereditary optic neuropathy : Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial dna mutation?CHINNERY, Patrick F; ANDREWS, Richard M; TURNBULL, Douglass M et al.American journal of medical genetics. 2001, Vol 98, Num 3, pp 235-243, issn 0148-7299Article

A New Phenotype of Brain Iron Accumulation with Dystonia, Optic Atrophy, and Peripheral NeuropathyHORVATH, Rita; HOLINSKI-FEDER, Elke; NURNBERG, Peter et al.Movement disorders. 2012, Vol 27, Num 6, pp 789-793, issn 0885-3185, 5 p.Article

Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathyKLEBE, Stephan; DEPIENNE, Christel; DOLLFUS, Hélène et al.Brain. 2012, Vol 135, pp 2980-2993, issn 0006-8950, 14 p., 10Article

A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathyKLOPSTOCK, Thomas; YU-WAI-MAN, Patrick; KERNT, Marcus et al.Brain. 2011, Vol 134, pp 2677-2686, issn 0006-8950, 10 p., 9Article

Page / 3