mtDNA: Pathogenic or nonpathogenic sequence changes.

Por Poulton, J., Bindoff, L. A.
Publicado em 1994

Facial vasculitic rash associated with intravenous immunoglobulin

Por Howse, M, Bindoff, L, Carmichael, A
Publicado em 1998

Methylprednisolone in multiple sclerosis: a comparative dose study.

Por Bindoff, L, Lyons, P R, Newman, P K, Saunders, M
Publicado em 1988

Carnitine palmitoyltransferase deficiency.

Por Bindoff, L A, Sherratt, H S, Singh, R, Turnbull, D M
Publicado em 1988

The investigation of mitochondrial respiratory chain disease.

Por Morris, A A, Jackson, M J, Bindoff, L A, Turnbull, D M
Publicado em 1995

Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tract

Por Chinnery, P, Jones, S, Sviland, L, Andrews, R, Parsons, T, Turnbull, D, Bindoff, L
Publicado em 2001

Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changes.

Por Bidooki, S K, Johnson, M A, Chrzanowska-Lightowlers, Z, Bindoff, L A, Lightowlers, R N
Publicado em 1997

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema

Por Tzoulis, C., Sztromwasser, Paweł, Johansson, Stefan, Gjerde, Ivar Otto, Knappskog, Per, Bindoff, L. A.
Publicado no Cerebellum (2016)

Combined enzyme defect of mitochondrial fatty acid oxidation.

Por Jackson, S, Kler, R S, Bartlett, K, Briggs, H, Bindoff, L A, Pourfarzam, M, Gardner-Medwin, D, Turnbull, D M
Publicado em 1992

A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle.

Por Weber, K, Wilson, J N, Taylor, L, Brierley, E, Johnson, M A, Turnbull, D M, Bindoff, L A
Publicado em 1997

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.

Por Howell, N, Bindoff, L A, McCullough, D A, Kubacka, I, Poulton, J, Mackey, D, Taylor, L, Turnbull, D M
Publicado em 1991

Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.

Por Watmough, N J, Bindoff, L A, Birch-Machin, M A, Jackson, S, Bartlett, K, Ragan, C I, Poulton, J, Gardiner, R M, Sherratt, H S, Turnbull, D M
Publicado em 1990

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

Joint meeting of the Association of British Neurologists and the Norwegian Neurological Association on the coastal steamer Hurtigruten, 6-9 May 2001

Por Bindoff, L, Hilton-Jones, D, Loseth, S, Torbergsen, T, Brautaset, N., Stalberg, E, Chinnery, P., Dearlove, A, Johnson, M., Walls, T., Gibson, G., Fawcett, P., Jamieson, S, Fulthorpe, J., Cullen, M, Hudgson, P, Bushby, K., Brathen, G, Sand, T, Michler, R, Brodtkorb, E, Helde, G, Bovim, G, Zeman, A, Stone, J, Porteous, M, Barron, L, Warner, J, Donaghy, M, Vedeler, C, Hallin, R., Bekkelund, S., Pierre-Jerome, C, Newsom-Davis, J, McConville, J, Kennett, R, Anslow, P, Hoch, W, Vincent, A, Orstavik, K, Schmidt, R, Jorum, E, Chmelz, S., Weidner, C, Hilliges, M, Torebjork, E, Nyland, H, Skeidsvold, H, Thorsen, E, Thrush, D, Miller, D., Russell, D, Bracewell, R., Wing, A., Nilsen, K., Kristiansen, T, Sand, T, Garseth, M, Stovner, L., Westgaard, R, Johnson, M., Ford, H, Denton, S, Bo, L, Nyland, H, Vedeler, C, Trapp, B., Mork, S, Midgard, R, Ebers, G, Kampmann, M, Parratt, J., Wilson, S, Donnan, P, O'riordan, J, Swingler, S, Harbo, H., Celius, E., Dai, K, Vartdal, F, Vandvik, B, Spurkland, A, Brex, P., Ciccarelli, O, O'Riordan, J., Sailer, M, Thompson, A., Miller, D., Warlow, C., Thomassen, L, Waje-Andreassen, U, Maintz, C, Al, S, Warlow, C., Ronning, O., Lossius, M, Zeman, A, Roste, L, Tauboll, E, Krogenas, A, Isojarvi, J, Gjerstad, L, Dietrichs, E, Stevens, D, Smith, D., Vlies, M, Bartolo, R, Leach, J.
Publicado em 2001