An "overtrained" ophthalmologist responds

por VOTRUBA, M.
Publicado em 2001

Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q.

por Votruba, M, Moore, A T, Bhattacharya, S S
Publicado em 1997

Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

por Votruba, M, Moore, A T, Bhattacharya, S S
Publicado em 1998

Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy

por Votruba, M, Thiselton, D, Bhattacharya, S S
Publicado em 2003

Primary monophasic synovial sarcoma of the conjunctiva

por Votruba, M, Hungerford, J, Cornes, P G S, Mabey, D, Luthert, P
Publicado em 2002

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

Mitochondrial dysfunction in an Opa1(Q285STOP) mouse model of dominant optic atrophy results from Opa1 haploinsufficiency

por Kushnareva, Y, Seong, Y, Andreyev, A Y, Kuwana, T, Kiosses, W B, Votruba, M, Newmeyer, D D
Publicado no Cell Death Dis (2016)

The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy

por Majander, A., Robson, A.G., João, C., Holder, G.E., Chinnery, P.F., Moore, A.T., Votruba, M., Stockman, A., Yu-Wai-Man, P.
Publicado no Mitochondrion (2017)

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