Mutations of the mitochondrial ND1 gene as a cause of MELAS von Kirby, D M, McFarland, R, Ohtake, A, Dunning, C, Ryan, M T, Wilson, C, Ketteridge, D, Turnbull, D M, Thorburn, D R, Taylor, R W

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Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause disease von Dunning, CJ R, McKenzie, M, Sugiana, C, Lazarou, M, Silke, J, Connelly, A, Fletcher, J M, Kirby, D M, Thorburn, D R, Ryan, M T

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Leigh syndrome: Clinical features and biochemical and DNA abnormalities von Rahman, S., Blok, R. B., Dahl, H.-H. M., Danks, D. M., Kirby, D. M., Chow, C. W., Christodoulou, J., Thorburn, D. R.

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Respiratory chain complex I deficiency : An underdiagnosed energy generation disorder von KIRBY, D. M, CRAWFORD, M, CLEARY, M. A, DAHL, H.-H. M, DENNETT, X, THORBURN, D. R

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Transmitochondrial embryonic stem cells containing pathogenic mtDNA mutations are compromised in neuronal differentiation von Kirby, D. M. , Rennie, K. J. , Smulders-Srinivasan, T. K. , Acin-Perez, R. , Whittington, M. , Enriquez, J.-A. , Trevelyan, A. J. , Turnbull, D. M. , Lightowlers, R. N. 

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Respiratory chain enzyme analysis in muscle and liver von Thorburn, D R, Chow, C W, Kirby, D M

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Moving in the Open Daylight: Doc Evatt, an Australian at the United Nations von Hogan, Ashley, Kirby, Michael

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A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrin von Vincent, J. Bryan, Kirby, Dawn M, Nguyen, Thanh V, Vigh, Gyula

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The Importance of Liver Biopsy in the Investigation of Possible Mitochondrial Respiratory Chain Disease von Panetta, J., Gibson, K., Kirby, D. M., Thorburn, D. R., Boneh, A.

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The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy von Bruno, Claudio, Kirby, Denise M., Koga, Yasutoshi, Garavaglia, Barbara, Duran, Gloria, Santorelli, Filippo M., Shield, Lloyd K., Xia, Wenlang, Shanske, Sara, Goldstein, Jeffrey D., Iwanaga, Rikako, Akita, Yukihiro, Carrara, Franco, Davis, Andrew, Zeviani, Massimo, Thorburn, David R., DiMauro, Salvatore

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Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavin von Ogle, R F, Christodoulou, J, Fagan, E, Blok, R B, Kirby, D M, Seller, K L, Dahl, H H, Thorburn, D R

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Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolism von Thompson, G.N., Butt, W.W., Shann, F.A., Kirby, D.M., Henning, R.D., Howells, D.W., Osborne, A.

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Mechanism of neurodegeneration of neurons with mitochondrial DNA mutations von Abramov, Andrey Y., Smulders-Srinivasan, Tora K., Kirby, Denise M., Acin-Perez, Rebeca, Enriquez, José Antonio, Lightowlers, Robert N., Duchen, Michael R., Turnbull, Douglass M.

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The Clinical and Biochemical Spectrum of Human Pyruvate Dehydrogenase Complex Deficiency von BROWN, G. K., BROWN, R. M., SCHOLEM, R. D., KIRBY, D. M., DAHL, H-H. M.

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Human BAC-mediated rescue of the Friedreich ataxia knockout mutation in transgenic mice von Sarsero, Joseph P, Li, Lingli, Holloway, Timothy P, Voullaire, Lucille, Gazeas, Sophie, Fowler, Kerry J, Kirby, Denise M, Thorburn, David R, Galle, Adam, Cheema, Surindar, Koenig, Michel, Williamson, Robert, Ioannou, Panos A

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Mitochondrial electron transport chain defect presenting as hypoglycemia von Freckmann, Mary-Louise, Thorburn, David R., Kirby, Denise M., Kamath, K.Ramananda, Hammond, Judith, Dennett, Xenia, Christodoulou, John

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Iatrogenic arteriovenous fistula after endovenous mechanical thrombectomy von Caputo, Ben Christopher, Kirby, Lemuel

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Genital psoriasis is associated with significant impairment in quality of life and sexual functioning von Ryan, Caitriona, MD, Sadlier, Muriel, MBBCh, De Vol, Edward, PhD, Patel, Mahir, MD, Lloyd, Amanda Abramson, MD, Day, Antoinette, BS, Lally, Aoife, MD, Kirby, Brian, MD, Menter, Alan, MD

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The struggle for simplicity: Lord Cooke and fundamental rights von Kirby, M D

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Pregnancy in phenylketonuria: dietary treatment aimed at normalising maternal plasma phenylalanine concentration von Thompson, G N, Francis, D E, Kirby, D M, Compton, R

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