Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease von Burn, John, Barker, William A, Markham, Alex F, Curtis, Ann, Chinnery, Patrick F, Coulthard, Alan, Fey, Constanze, Jackson, Andrew P, Jackson, Margaret J, Bates, David, Curtis, Andrew R.J, McHale, Duncan P, Bindoff, Laurence A, Ince, Paul G, Hay, David, Morris, Christopher M

Volltext

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast von Blakely, Emma L., Mitchell, Anna L., Fisher, Nicholas, Meunier, Brigitte, Nijtmans, Leo G., Schaefer, Andrew M., Jackson, Margaret J., Turnbull, Douglass M., Taylor, Robert W.

Volltext

Concise guidance: diagnosis and management of the epilepsies in adults von Jackson, Margaret J

Volltext

Spectrum of movement disorders in neuroferritinopathy von Crompton, Douglas E., Chinnery, Patrick F., Bates, David, Walls, Timothy J., Jackson, Margaret J., Curtis, Andrew J., Burn, John

Volltext

Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation von Chinnery, Patrick F., Crompton, Douglas E., Birchall, Daniel, Jackson, Margaret J., Coulthard, Alan, Lombès, Anne, Quinn, Niall, Wills, Adrian, Fletcher, Nicholas, Mottershead, John P., Cooper, Paul, Kellett, Mark, Bates, David, Burn, John

Volltext

Neuroferritinopathy: A Window on the Role of Iron in Neurodegeneration von Crompton, Douglas E., Chinnery, Patrick F., Fey, Constanze, Curtis, Andrew R.J., Morris, Christopher M., Kierstan, Jo, Burt, Alistair, Young, Fergus, Coulthard, Alan, Curtis, Ann, Ince, Paul G., Bates, David, Jackson, Margaret J., Burn, John

Volltext

Should we accept the status quo? Time for new trials in status epilepticus von Jackson, Margaret J

Volltext

Choice of Antiepileptic Drug, Which One to Try First and What to Do if it Fails von Jackson, Margaret J

Volltext

Depression and anxiety in epilepsy von Jackson, M J, Turkington, D

Volltext

Choice of antiepileptic drug, which one to try first and what to do if it fails von Jackson, Margaret J

Volltext

Intravenous levetiracetam in the treatment of benzodiazepine refractory status epilepticus. Commentary von JACKSON, Margaret J, KNAKE, S, GRUENER, J, HATTEMER, K, KLEIN, K. M, BAUER, S, OERTEL, W. H, HAMER, H. M, ROSENOW, F

Volltext

Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain von MORRIS, A. A. M, TAYLOR, R. W, BIRCH-MACHIN, M. A, JACKSON, M. J, COULTHARD, M. G, BINDOFF, L. A, WELCH, R. J, HOWELL, N, TURNBULL, D. M

Volltext

Clinical features and natural history of neuroferritinopathy caused by the FTLI 460InsA mutation von CHINNERY, Patrick F, CROMPTON, Douglas E, COOPER, Paul, KELLETT, Mark, BATES, David, BURN, John, BIRCHALL, Daniel, JACKSON, Margaret J, COULTHARD, Alan, LOMBES, Anne, QUINN, Niall, WILLS, Adrian, FLETCHER, Nicholas, MOTTERSHEAD, John P

Volltext

A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis von Taylor, R W, Chinnery, P F, Bates, M J, Jackson, M J, Johnson, M A, Andrews, R M, Turnbull, D M

Volltext

Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxia von Taylor, Robert W., Birch-Machin, Mark A., Schaefer, Jochen, Taylor, Louise, Shakir, Raad, Ackrell, Brian A. C., Cochran, Bruce, Bindoff, Laurence A., Jackson, Margaret J., Griffiths, Philip, Turnbull, Douglass M.

Volltext

Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene von Bidooki, Seyed, Jackson, Margaret J, Johnson, Margaret A, Chrzanowska-Lightowlers, Zofia M.A, Taylor, Robert W, Venables, Graham, Lightowlers, Robert N, Turnbull, Douglass M, Bindoff, Laurence A

Volltext

Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNA Ser(UCN) gene von Bidooki, Seyed, Jackson, Margaret J, Johnson, Margaret A, Chrzanowska-Lightowlers, Zofia M.A, Taylor, Robert W, Venables, Graham, Lightowlers, Robert N, Turnbull, Douglass M, Bindoff, Laurence A

Volltext

Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene von Bidooki, Seyed, Jackson, Margaret J, Johnson, Margaret A, Chrzanowska-Lightowlers, Zofia M A, Taylor, Robert W, Venables, Graham, Lightowlers, Robert N, Turnbull, Douglass M, Bindoff, Laurence A

Volltext

A Novel Mitochondrial DNA Point Mutation in the tRNAIleGene: Studies in a Patient Presenting with Chronic Progressive External Ophthalmoplegia and Multiple Sclerosis von Taylor, Robert W., Chinnery, Patrick F., Bates, Matthew J.D., Jackson, Margaret J., Johnson, Margaret A., Andrews, Richard M., Turnbull, Douglass M.

Volltext

Cortical blindness during left internal mammary angiography von Skinner, Jane S., Jackson, Margaret J., Gholkar, Anil, Adams, Philip C.

Volltext