Sight tests to detect glaucoma. Reliability of screening procedures and effectiveness of treatment need to be assessed.

Por Griffiths, P. G.
Publicado em 1997

Vision screening in preschool children.

Por Griffiths, P. G., Clarke, M.
Publicado em 1992

Drop sizes of commonly used topical β blockers

Por Griffiths, P G, Stirling, R J
Publicado em 1991

Effect on mydriasis of modifying the volume of phenylephrine drops.

Por Craig, E W, Griffiths, P G
Publicado em 1991

Adherence of Staphylococcus epidermidis to intraocular lenses.

Por Griffiths, P. G., Elliot, T. S., McTaggart, L.
Publicado em 1989

Reducing unnecessary investigation of anterior uveitis

Por Bell, R W D, Griffiths, P G, Goodwin, D
Publicado em 1994

Inherited mitochondrial optic neuropathies

Por Yu-Wai-Man, P, Griffiths, P G, Hudson, G, Chinnery, P F
Publicado em 2009

Eye movement recordings to investigate a supranuclear component in chronic progressive external ophthalmoplegia: a cross-sectional study

Por Ritchie, A E, Griffiths, P G, Chinnery, P F, Davidson, A W
Publicado em 2010

A Supranuclear Disorder of Ocular Motility as a Rare Initial Presentation of Motor Neurone Disease

Por Yu-Wai-Man, C., Petheram, K., Davidson, A. W., Williams, T., Griffiths, P. G.
Publicado no Neuroophthalmology (2011)

Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations

Por Yu-Wai-Man, P, Bailie, M, Atawan, A, Chinnery, P F, Griffiths, P G
Publicado em 2011

The role of mitochondrial haplogroups in primary open angle glaucoma

Por Andrews, R, Ressiniotis, T, Turnbull, D M, Birch, M, Keers, S, Chinnery, P F, Griffiths, P G
Publicado em 2006

The Epidemiology of Leber Hereditary Optic Neuropathy in the North East of England

Por Yu-Wai-Man, P., Griffiths, P.G., Howell, N., Turnbull, D.M., Chinnery, P.F.
Publicado no Am J Hum Genet (2016)

The Epidemiology of Leber Hereditary Optic Neuropathy in the North East of England

Por Man, P. Y. W., Griffiths, P. G., Brown, D. T., Howell, N., Turnbull, D. M., Chinnery, P. F.
Publicado em 2003

Subclinical multisystem neurologic disease in “pure” OPA1 autosomal dominant optic atrophy

Por Baker, M.R., Fisher, K.M., Whittaker, R.G., Griffiths, P.G., Yu-Wai-Man, P., Chinnery, P.F.
Publicado em 2011

Persistence of the treatment effect of idebenone in Leber’s hereditary optic neuropathy

Por Klopstock, T., Metz, G., Yu-Wai-Man, P., Büchner, B., Gallenmüller, C., Bailie, M., Nwali, N., Griffiths, P. G., von Livonius, B., Reznicek, L., Rouleau, J., Coppard, N., Meier, T., Chinnery, P. F.
Publicado em 2013

Multi-system neurological disease is common in patients with OPA1 mutations

Por Yu-Wai-Man, P., Griffiths, P.G., Gorman, G.S., Lourenco, C.M., Wright, A.F., Auer-Grumbach, M., Toscano, A., Musumeci, O., Valentino, M.L., Caporali, L., Lamperti, C., Tallaksen, C.M., Duffey, P., Miller, J., Whittaker, R.G., Baker, M.R., Jackson, M.J., Clarke, M.P., Dhillon, B., Czermin, B., Stewart, J.D., Hudson, G., Reynier, P., Bonneau, D., Marques, W., Lenaers, G., McFarland, R., Taylor, R.W., Turnbull, D.M., Votruba, M., Zeviani, M., Carelli, V., Bindoff, L.A., Horvath, R., Amati-Bonneau, P., Chinnery, P.F.
Publicado em 2010