Methylene blue induced O2 consumption is not dependent on mitochondrial oxidative phosphorylation: Implications for salvage pathways during acute mitochondrial poisoning von Bouillaud, F., Ransy, C., Moreau, M., Benhaim, J., Lombès, A., Haouzi, P.

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Prediction of long‐term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke‐like episodes sy... von Fayssoil, A., Laforêt, P., Bougouin, W., Jardel, C., Lombès, A., Bécane, H. M., Berber, N., Stojkovic, T., Béhin, A., Eymard, B., Duboc, D., Wahbi, K.

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Neuroferritinopathy in a French family with late onset dominant dystonia von Chinnery, P F, Curtis, A R J, Fey, C, Coulthard, A, Crompton, D, Curtis, A, Lombés, A, Burn, J

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Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis von Medja, F, Allouche, S, Frachon, P, Jardel, C, Malgat, M, Mousson de Camaret, B, Slama, A, Lunardi, J, Mazat, J P, Lombès, A

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Cardiac involvement is frequent in patients with the m.8344A>G mutation of mitochondrial DNA von WAHBI, K, LARUE, S, JARDEL, C, MEUNE, C, STOJKOVIC, T, ZIEGLER, F, LOMBES, A, EYMARD, B, DUBOC, D, LAFORET, P

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Adult cases of mitochondrial DNA depletion due to TK2 defect: An expanding spectrum von BEHIN, A, JARDEL, C, CLAEYS, K. G, FAGART, J, LOUHA, M, ROMERO, N. B, LAFORET, P, EYMARD, B, LOMBES, A

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Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1 von LE BER, I, DUBOURG, O, BENOIST, J.-F, JARDEL, C, MOCHEL, F, KOENIG, M, BRICE, A, LOMBES, A, DÜRR, A

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Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation von Saada, A, Shaag, A, Arnon, S, Dolfin, T, Miller, C, Fuchs-Telem, D, Lombes, A, Elpeleg, O

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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

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Modulation of mitochondrial morphology by bioenergetics defects in primary human fibroblasts von Guillery, O, Malka, F, Frachon, P, Milea, D, Rojo, M, Lombès, A

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Life-threatening lactic acidosis occurring in adults with mitochondrial disorders von Brisset, M., Béhin, A., Pottier, C., Jardel, C., Sharshar, T., Mochel, F., Mallard, F., Slama, A., Lombès, A., Eymard, B., Laforêt, P.

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The mitochondrial complex i inhibitor annonacin is toxic to mesencephalic dopaminergic neurons by impairment of energy metabolism von Lannuzel, A, Michel, P.P, Höglinger, G.U, Champy, P, Jousset, A, Medja, F, Lombès, A, Darios, F, Gleye, C, Laurens, A, Hocquemiller, R, Hirsch, E.C, Ruberg, M

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Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase Deficiency von Kaphan, E., Bou Ali, H., Gastaldi, M., Acquaviva, C., Vianey-Saban, C., Rouzier, C., Fragaki, K., Bannwarth, S., Paquis-Flucklinger, V., Romero, N., Behin, A., Lombès, A., Jardel, C., Rigal, O., Laforêt, P.

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Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene von Zsurka, G, Hampel, K G, Nelson, I, Jardel, C, Mirandola, S R, Sassen, R, Kornblum, C, Marcorelles, P, Lavoué, S, Lombès, A, Kunz, W S

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A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure von Tzagoloff, Alexander, Niaudet, Patrick, Barrientos, Antoni, Munnich, Arnold, Rustin, Pierre, Taanman, Jan-Willem, Chrétien, Dominique, Kadhom, Noman, Rötig, Agnès, Benayoun, Emmanuel, Lombès, Anne, Valnot, Isabelle, de Lonlay, Pascale, Gorbatyuk, Marina, de Baulny, Hélène Ogier

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Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1) von Poulton, J., Hirano, M., Spinazzola, A., Arenas Hernandez, M., Jardel, C., Lombès, A., Czermin, B., Horvath, R., Taanman, J.W., Rotig, A., Zeviani, M., Fratter, C.

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A novel mutation 3090 G > A of the mitochondrial 16S ribosomal RNA associated with myopathy von Coulbault, L., Deslandes, B., Herlicoviez, D., Read, M.H., Leporrier, N., Schaeffer, S., Mouadil, A., Lombès, A., Chapon, F., Jauzac, P., Allouche, S.

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NAMPT inhibition is a novel synthetic lethal therapeutic approach exploiting nuclear–mitochondrial crosstalk in ERCC1-deficient populations von Touat, M, Olaussen, K, Sourisseau, T, Friboulet, L, Dorvault, N, Enot, D, Bigot, L, Pontoizeau, C, Mardakheh, F, Thompson, A, Bouillaud, F, Ricchetti, M, Ottolenghi, C, Pierron, G, Sarasin, A, Lombès, A, Ashworth, A, Lord, C, Soria, J.C, Postel-Vinay, S

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Zidovudine-induced mitochondrial disorder with massive liver steatosis, myopathy, lactic acidosis, and mitochondrial DNA depletion von Chariot, Patrick, Drogou, Irène, Lacroix-Szmania, Isabelle de, Eliezer-Vanerot, Marie-Christine, Chazaud, Bénédicte, Lombès, Anne, Schaeffer, Annette, Zafrani, Elie Serge

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G.P.189 von Péréon, Y, Magot, A, Fayet, G, Mercier, S, Mussini, J.M, Auré, K, Lombès, A, Jardel, C

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