Late-onset idiopathic focal dystonia of the trunk: A treatable cause of bent spine syndrome von Hainque, E., Apartis, E., Tarrano, C., Karachi, C., Roze, E.

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Switching between two targets with non-constant velocity profiles reveals shared internal model of target motion von Hainque, E., Apartis, E., Daye, P. M.

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Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein von Mariani, L. L., Rivaud-Péchoux, S., Charles, P., Ewenczyk, C., Meneret, A., Monga, B. B., Fleury, M.-C., Hainque, E., Maisonobe, T., Degos, B., Echaniz-Laguna, A., Renaud, M., Wirth, T., Grabli, D., Brice, A., Vidailhet, M., Stoppa-Lyonnet, D., Dubois-d’Enghien, C., Le Ber, I., Koenig, M., Roze, E., Tranchant, C., Durr, A., Gaymard, B., Anheim, M.

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A clinical and neurophysiological motor signature of Unverricht–Lundborg disease von Hainque, E., Blancher, A., Mesnage, V., Rivaud-Pechoux, S., Bertrand, A., Dupont, S., Navarro, V., Roze, E., Gourfinkel-An, I., Apartis, E.

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A simple blood test expedites the diagnosis of GLUT1 deficiency syndrome von Gras, D, Cousin, C, Kappeler, C, Auvin, S, Essid, N, Da Costa, L, Hainque, E, Luton, M.P, Petit, V, Vuillaumier-Barrot, S, Boespflug-Tanguy, O, Roze, E, Mochel, F

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Severe dysautonomia revealing Wernicke's encephalopathy von Cognat, E, Hainque, E, Mesnage, V, Levy, R

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Dysautonomie sévère révélatrice d’une encéphalopathie de Gayet-Wernicke von Cognat, E., Hainque, E., Mesnage, V., Levy, R.

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Infarctus médullaire par compression d’une artère lombaire par le pilier droit du diaphragme von Lagarde, J., Hainque, E., Biondi, A., Lacroix, D., Mesnage, V., Levy, R.

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Usefulness of mismatch negativity for simple cognitive dysfunction assessment in multiple sclerosis patients von Hainque, E, Daniel, F, Lebrun, N, Etard, O, Defer, G

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Spinal cord infarction due to compression of a lumbar artery by the right diaphragmatic crus von Lagarde, J, Hainque, E, Biondi, A, Lacroix, D, Mesnage, V, Levy, R

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G - 34 Anévrismes cérébraux et systémiques multiples, dysplasie fibromusculaire et myxome cardiaque : un cas clinique von Hainque, E., Guillamo, J.-S., Galateau-Salle, F., Maïza, D., Defer, G.L.

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Spinal cord infarction due to compression of a lumbar artery by the right diaphragmatic crus von Lagarde, J, Hainque, E, Biondi, A, Lacroix, D, Mesnage, V, Levy, R

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Systemic low-grade inflammation is related to both circulating and adipose tissue TNFα, leptin and IL-6 levels in obese women von MAACHI, M, PIERONI, L, BRUCKERT, E, JARDEL, C, FELLAHI, S, HAINQUE, B, CAPEAU, J, BASTARD, J-P

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Electrochemical DNA-biosensors based on long-range electron transfer: optimization of the amperometric detection in the femtomolar range using two-electrode setup and ultramicroele... von Nassi, A., Guillon, F.-X., Amar, A., Hainque, B., Amriche, S., Maugé, D., Markova, E., Tsé, C., Bigey, P., Lazerges, M., Bedioui, F.

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Adipose tissue IL-6 content correlates with resistance to insulin activation of glucose uptake both in vivo and in vitro von BASTARD, Jean-Philippe, MAACHI, Mustapha, VAN NHIEU, Jeanne Tran, JARDEL, Claude, BRUCKERT, Eric, GRIMALDI, André, ROBERT, Jean-Jacques, CAPEAU, Jacqueline, HAINQUE, Bernard

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Elevated levels of interleukin 6 are reduced in serum and subcutaneous adipose tissue of obese women after weight loss von BASTARD, Jean-Philippe, JARDEL, Claude, BRUCKERT, Eric, BLONDY, Patricia, CAPEAU, Jacqueline, LAVILLE, Martine, VIDAL, Hubert, HAINQUE, Bernard

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Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy von Gandjbakhch, E, Charron, P, Fressart, V, Lorin de la Grandmaison, G, Simon, F, Gary, F, Vite, A, Hainque, B, Hidden-Lucet, F, Komajda, M, Villard, E

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Low incidence of cardiac events with β-blocking therapy in children with long QT syndrome von Villain, E., Denjoy, I., Lupoglazoff, J.M., Guicheney, P., Hainque, B., Lucet, V., Bonnet, D.

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Long QT syndrome in neonates: Conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations von LUPOGLAZOFF, Jean-Marc, DENJOY, Isabelle, VILLAIN, Elisabeth, FRESSART, Véronique, SIMON, Francoise, BOZIO, André, BERTHET, Myriam, BENAMMAR, Nawal, HAINQUE, Bernard, GUICHENEY, Pascale

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New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis von VICART, S, STERNBERG, D, FOURNIER, E, OCHSNER, F, LAFORET, P, KUNTZER, T, EYMARD, B, HAINQUE, B, FONTAINE, B

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