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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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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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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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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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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P.17.15 Life-threatening lactic acidosis occurring in adults with rare mutations of mtDNA: About three cases von Laforêt, P, Pottier, C, Behin, A, Gilleron, M, Sharshar, T, Lombes, A, Jardel, C, Eymard, B

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G.P.186 von Fayet, G, Aure, K, Lesimple, P, L’Hermitte-Stead, C, Chevalier, C, Magot, A, Houlgatte, R, Pereon, Y, Lombes, A, Savagner, F

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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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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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Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disorders von Angelini, C., Federico, A., Reichmann, H., Lombes, A., Chinnery, P., Turnbull, D.

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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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Myoblast Xenotransplantation as a Tool to Evaluate the Appropriateness of Nanoparticular versus Cellular Trackers von Praud, C., Vauchez, K., Lombes, A., Fiszman, M. Y., Vilquin, J.-T.

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A novel FTL insertion causing neuroferritinopathy von Batey, S, Vuillaume, I, Devos, D, Destée, A, Curtis, A J, Lombes, A, Curtis, A, Burn, J, Chinnery, P F

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Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins von Legros, Frédéric, Lombès, Anne, Frachon, Paule, Rojo, Manuel

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Les approches lipidomiques et métabolomiques identifient les MAM (mitochondria-associated membranes) comme la cible cellulaire du mitotane von Hescot, S, Lhomme, M, Dubow, A, Amazit, L, Travers, S, Battini, S, Namer, I, Lombes, A, Kontush, A, Paci, A, Imperiale, A, Baudin, E, Lombes, M

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CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures von Mollet, Julie, Delahodde, Agnès, Serre, Valérie, Chretien, Dominique, Schlemmer, Dimitri, Lombes, Anne, Boddaert, Nathalie, Desguerre, Isabelle, de Lonlay, Pascale, Ogier de Baulny, Hélène, Munnich, Arnold, Rötig, Agnès

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Organization and dynamics of human mitochondrial DNA von Legros, Frédéric, Malka, Florence, Frachon, Paule, Lombès, Anne, Rojo, Manuel

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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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Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo von Rojo, Manuel, Legros, Frédéric, Chateau, Danielle, Lombès, Anne

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