List of works - Philip Griffiths

A passive house with seasonal solar energy store:in situdata and numerical modelling

article by Joshua Clarke et al published 12 March 2013 in International Journal of Ambient Energy

A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy

scientific article

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

scientific article

Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegia

scientific article

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder

scientific article

Inherited mitochondrial optic neuropathies

scientific article

Investigation of auditory dysfunction in Leber hereditary optic neuropathy

scientific article published in September 2008

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

scientific article

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies

scientific article

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

scientific article

Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism

scientific article published on 01 April 2007

OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules

scientific article

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

scientific article published on 14 October 2010

Observed site obstacle impacts on the energy performance of a large scale urban wind turbine using an electrical energy rose

Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.

scientific article published in July 2005

Quality of life in patients with leber hereditary optic neuropathy

scientific article

Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic Neuropathy

scientific article

Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular muscles

scientific article

The prevalence and natural history of dominant optic atrophy due to OPA1 mutations

scientific article

Thermal energy storage in building integrated thermal systems: A review. Part 2. Integration as passive system

article

Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON.

scientific article

Visual and psychological morbidity among patients with autosomal dominant optic atrophy

scientific article published on 4 March 2013

List of works by Philip Griffiths

A passive house with seasonal solar energy store:in situdata and numerical modelling

A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegia

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder

Inherited mitochondrial optic neuropathies

Investigation of auditory dysfunction in Leber hereditary optic neuropathy

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism

OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules

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

Observed site obstacle impacts on the energy performance of a large scale urban wind turbine using an electrical energy rose

Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.

Quality of life in patients with leber hereditary optic neuropathy

Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic Neuropathy

Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular muscles

The prevalence and natural history of dominant optic atrophy due to OPA1 mutations

Thermal energy storage in building integrated thermal systems: A review. Part 2. Integration as passive system

Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON.

Visual and psychological morbidity among patients with autosomal dominant optic atrophy