Quantification of acetogenins in Annona muricata linked to atypical parkinsonism in guadeloupe von Champy, Pierre, Melot, Alice, Guérineau Eng, Vincent, Gleye, Christophe, Fall, Djibril, Höglinger, Gunter U., Ruberg, Merle, Lannuzel, Annie, Laprévote, Olivier, Laurens, Alain, Hocquemiller, Reynald

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Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia von Depienne, Christel, Fedirko, Estelle, Forlani, Sylvie, Cazeneuve, Cécile, Ribaï, Pascale, Feki, Imed, Tallaksen, Chantal, Nguyen, Karine, Stankoff, Bruno, Ruberg, Merle, Stevanin, Giovanni, Durr, Alexandra, Brice, Alexis

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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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Atypical parkinsonism in Guadeloupe: a common risk factor for two closely related phenotypes? von Lannuzel, Annie, Höglinger, G. U., Verhaeghe, S., Gire, L., Belson, S., Escobar-Khondiker, M., Poullain, P., Oertel, W. H., Hirsch, E. C., Dubois, B., Ruberg, M.

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Metabolic activity of cerebellar and basal ganglia-thalamic neurons is reduced in parkinsonism von Rolland, Anne-Sophie, Herrero, Maria-Trinidad, Garcia-Martinez, Virginia, Ruberg, Merle, Hirsch, Etienne C., François, Chantal

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years von Namekawa, M, Ribai, P, Nelson, I, Forlani, S, Fellmann, F, Goizet, C, Depienne, C, Stevanin, G, Ruberg, M, Dürr, A, Brice, A

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations von AZZEDINE, H, RAVISE, N, HAMADOUCHE, T, BOUHOUCHE, A, GUILBOT, A, STENDEL, C, RUBERG, M, BRICE, A, BIROUK, N, DUBOURG, O, TAZIR, M, LEGUERN, E, VERNY, C, GABRËELS-FESTEN, A, LAMMENS, M, GRID, D, VALLAT, J. M, DUROSIER, G, SENDEREK, J, NOUIOUA, S

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Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis von Namekawa, M., Muriel, M.-P., Janer, A., Latouche, M., Dauphin, A., Debeir, T., Martin, E., Duyckaerts, C., Prigent, A., Depienne, C., Sittler, A., Brice, A., Ruberg, M.

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Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease von Dubourg, O, Azzedine, H, Verny, C, Durosier, G, Birouk, N, Gouider, R, Salih, M, Bouhouche, A, Thiam, A, Grid, D, Mayer, M, Ruberg, M, Tazir, M, Brice, A, LeGuern, E

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Quality of spirometry and related diagnosis in primary care with a focus on clinical use von van de Hei, S. J., Flokstra-de Blok, B. M. J., Baretta, H. J., Doornewaard, N. E., van der Molen, T., Patberg, K. W., Ruberg, E. C. M., Schermer, T. R. J., Steenbruggen, I., van den Berg, J. W. K., Kocks, J. W. H.

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New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p von NABBOUT, R, BAULAC, S, DESGUERRE, I, BAHI-BUISSON, N, CHIRON, C, RUBERG, M, DULAC, O, LEGUERN, E

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The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V von DUBOURG, O, AZZEDINE, H, BEN YAOU, R, POUGET, J, BAROIS, A, MEININGER, V, BOUTEILLER, D, RUBERG, M, BRICE, A, LEGUERN, E

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Re-evaluation of the functional anatomy of the basal ganglia in normal and Parkinsonian states von Levy, R., Hazrati, L.-N., Herrero, M.-T., Vila, M., Hassani, O.-K., Mouroux, M., Ruberg, M., Asensi, H., Agid, Y., Féger, J., Obeso, J.A., Parent, A., Hirsch, E.C.

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Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families von Bouhouche, Ahmed, Birouk, Nazha, Azzedine, Hamid, Benomar, Ali, Durosier, Garry, Ente, Dorothée, Muriel, Marie-Paule, Ruberg, Merle, Slassi, Ilham, Yahyaoui, Mohamed, Dubourg, Odile, Ouazzani, Reda, LeGuern, Eric

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Evolution of changes in neuronal activity in the subthalamic nucleus of rats with unilateral lesion of the substantia nigra assessed by metabolic and electrophysiological measureme... von Vila, M., Périer, C., Féger, J., Yelnik, J., Faucheux, B., Ruberg, M., Raisman-Vozari, R., Agid, Y., Hirsch, E. C.

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Metabolic activity of excitatory parafascicular and pedunculopontine inputs to the subthalamic nucleus in a rat model of Parkinson's disease von Orieux, G., Francois, C., Féger, J., Yelnik, J., Vila, M., Ruberg, M., Agid, Y., Hirsch, E.C.

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De Novo Expansion of Intermediate Alleles in Spinocerebellar Ataxia 7 von Stevanin, Giovanni, Giunti, Paola, David, Gilles, Belal, Samir, Dürr, Alexandra, Ruberg, Merle, Wood, Nicholas, Brice, Alexis

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Subthalamotomy in parkinsonian monkeys Behavioural and biochemical analysis von Guridi, J., Herrero, M. T., Luquin, M. R., Guillén, J., Ruberg, M., Laguna, J., Vila, M., Javoy-Agid, F., Agid, Y., Hirsch, E., Obeso, J. A.

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Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene von Azzedine, H, Ruberg, M, Ente, D, Gilardeau, C, Périé, S, Wechsler, B, Brice, A, LeGuern, E, Dubourg, O

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Natural lipophilic inhibitors of mitochondrial complex I are candidate toxins for sporadic neurodegenerative tau pathologies von Höllerhage, Matthias, Matusch, Andreas, Champy, Pierre, Lombès, Anne, Ruberg, Merle, Oertel, Wolfgang H., Höglinger, Günter U.

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