Genetics of mitochondrial diseases

Por Chinnery, P
Publicado em 2004

Neuroscience for neurologists

Por Chinnery, P, Kennard, C
Publicado em 2003

Mitochondria

Por Chinnery, P, Schon, E
Publicado em 2003

Clinical features, investigation, and management of patients with defects of mitochondrial DNA

Por CHINNERY, P., TURNBULL, D.
Publicado em 1997

Relaxed replication of mtDNA: A model with implications for the expression of disease.

Por Chinnery, P F, Samuels, D C
Publicado em 1999

Leber hereditary optic neuropathy

Por Man, P, Turnbull, D, Chinnery, P
Publicado em 2002

Next generation sequencing for neurological diseases: New hope or new hype?

Por Keogh, M.J., Chinnery, P.F.
Publicado em 2013

Informed consent in clinical trials. Consent may not be possible.

Por Chinnery, P, Asimakopoulos, G, Kenny, R A
Publicado em 1993

No evidence of an association between the mtDNA 16184-93 polyC tract and late onset dementia

Por Keers, S, Gibson, A, Turnbull, D, Chinnery, P
Publicado em 2004

Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy

Por Taylor, R, Jobling, M, Turnbull, D, Chinnery, P
Publicado em 2003

Primary open angle glaucoma is associated with a specific p53 gene haplotype

Por Ressiniotis, T, Griffiths, P, Birch, M, Keers, S, Chinnery, P
Publicado em 2004

Clinical mitochondrial genetics

Por Chinnery, P., Howell, N., Andrews, R., Turnbull, D.
Publicado em 1999

Mitochondrial DNA analysis: polymorphisms and pathogenicity

Por Chinnery, P., Howell, N., Andrews, R., Turnbull, D.
Publicado em 1999

The inheritance of pathogenic mitochondrial DNA mutations

Por Cree, L.M., Samuels, D.C., Chinnery, P.F.
Publicado em 2009

An under-recognised cause of spastic paraparesis in middle-aged women

Por Bargiela, D, Eglon, G, Horvath, R, Chinnery, P F
Publicado em 2013

Spinocerebellar ataxia and the A3243G and A8344G mtDNA mutations

Por Chinnery, P, Brown, D, Archibald, K, Curtis, A, Turnbull, D
Publicado em 2002

Mitochondrial DNA mutations and pathogenicity.

Por Chinnery, P F, Turnbull, D M, Howell, N, Andrews, R M
Publicado em 1998

Genetic counseling and prenatal diagnosis for mtDNA disease.

Por Chinnery, P F, Howell, N, Lightowlers, R N, Turnbull, D M
Publicado em 1998

Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31

Por Fisher, K. M., Chinnery, P. F., Baker, S. N., Baker, M. R.
Publicado em 2013

Treatment strategies for inherited optic neuropathies: past, present and future

Por Yu-Wai-Man, P, Votruba, M, Moore, A T, Chinnery, P F
Publicado em 2014