Inherited mitochondrial optic neuropathies von Yu-Wai-Man, P, Griffiths, P G, Hudson, G, Chinnery, P F

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Treatment strategies for inherited optic neuropathies: past, present and future von Yu-Wai-Man, P, Votruba, M, Moore, A T, Chinnery, P F

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Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis von MATTHEWS, E, LABRUM, R, HANNA, M. G, SWEENEY, M. G, SUD, R, HAWORTH, A, CHINNERY, P. F, MEOLA, G, SCHORGE, S, KULLMANN, D. M, DAVIS, M. B

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

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T2 and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation von MCNEILL, A, BIRCHALL, D, HAYFLICK, S. J, GREGORY, A, SCHENK, J. F, ZIMMERMAN, E. A, SHANG, H, MIYAJIMA, H, CHINNERY, P. F

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A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy von HICKS, Debbie, SARKOZY, Anna, BAILEY, Geraldine, MILLER, James, RADUNOVIC, Aleksander, HUGHES, Paul J, ROBERT, Richard, KRAUSE, Sabine, WALTER, Maggie C, LAVAL, Steven H, STRAUB, Volker, LOCHMÜLLER, Hanns, MUELAS, Nuria, BUSHBY, Kate, KÖEHLER, Katrin, HUEBNER, Angela, HUDSON, Gavin, CHINNERY, Patrick F, BARRESI, Rita, EAGLE, Michelle, POLVIKOSKI, Tuomo

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Inheritance of mitochondrial DNA in humans: implications for rare and common diseases von Wei, W., Chinnery, P. F.

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The Epidemiology of Leber Hereditary Optic Neuropathy in the North East of England von Man, P.Y.W., Griffiths, P.G., Brown, D.T., Howell, N., Turnbull, D.M., Chinnery, P.F.

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Leber hereditary optic neuropathy von Man, P Y W, Turnbull, D M, Chinnery, P F

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THE MINIMUM PREVALENCE OF CADASIL IN NORTHEAST ENGLAND von NARAYAN, S. K, GORMAN, G, KALARIA, R. N, FORD, G. A, CHINNERY, P. F

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Mitochondria von Chinnery, P F, Schon, E A

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Random Intracellular Drift Explains the Clonal Expansion of Mitochondrial DNA Mutations with Age von Elson, J.L., Samuels, D.C., Turnbull, D.M., Chinnery, P.F.

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Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA von Andrews, Richard M., Kubacka, Iwona, Chinnery, Patrick F., Lightowlers, Robert N., Turnbull, Douglass M., Howell, Neil

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The Pedigree Rate of Sequence Divergence in the Human Mitochondrial Genome: There Is a Difference Between Phylogenetic and Pedigree Rates von Howell, Neil, Smejkal, Christy Bogolin, Mackey, D.A., Chinnery, P.F., Turnbull, D.M., Herrnstadt, Corinna

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The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO von FRATTER, C, GORMAN, G. S, RAHMAN, S, OMER, S. E, KLOPSTOCK, T, SCHOSER, B, KORNBLUM, C, CZERMIN, B, LECKY, B, BLAKELY, E. L, CRAIG, K, CHINNERY, P. F, STEWART, J. D, TURNBULL, D. M, HORVATH, R, TAYLOR, R. W, BUDDLES, M, SMITH, C, EVANS, J, SELLER, A, POULTON, J, ROBERTS, M, HANNA, M. G

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Clinical features of hereditary spastic paraplegia due to spastin mutation von MCDERMOTT, C. J, BURNESS, C. E, SHAW, P. J, KIRBY, J, COX, L. E, RAO, D. G, HEWAMADDUMA, C, SHARRACK, B, HADJIVASSILIOU, M, CHINNERY, P. F, DALTON, A

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OPA1 increases the risk of normal but not high tension glaucoma von Yu-Wai-Man, P, Stewart, J D, Hudson, G, Andrews, R M, Griffiths, P G, Birch, M K, Chinnery, P F

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RRM2B MUTATIONS ARE FREQUENT IN FAMILIAL PEO WITH MULTIPLE mtDNA DELETIONS von FRATTER, C, RAMAN, P, POULTON, J, BRIERLEY, C, STAUNTON, T. G, TURNPENNY, P. D, SCHAEFER, A. M, CHINNERY, P. F, HORVATH, R, TURNBULL, D. M, GORMAN, G. S, TAYLOR, R. W, ALSTON, C. L, BLAKELY, E. L, CRAIG, K, SMITH, C, EVANS, J, SELLER, A, CZERMIN, B, HANNA, M. G

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Mitochondrial disease in adults: a scale to monitor progression and treatment von Schaefer, A M, Phoenix, C, Elson, J L, McFarland, R, Chinnery, P F, Turnbull, D M

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The epidemiology of pathogenic mitochondrial DNA mutations von Chinnery, P. F., Johnson, M. A., Wardell, T. M., Singh-Kler, R., Hayes, C., Brown, D. T., Taylor, R. W., Bindoff, L. A., Turnbull, D. M.

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