Search Results - "Wargon, Isabelle"

Impaired efficacy of spinal presynaptic mechanisms in spastic stroke patients by Lamy, Jean-Charles, Wargon, Isabelle, Mazevet, Dominique, Ghanim, Zaïd, Pradat-Diehl, Pascale, Katz, Rose

“…Pathophysiological mechanisms underlying spasticity have been the subject of many studies. These studies performed in various kinds of spastic patients have…”
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C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing by Le Ber, Isabelle, Camuzat, Agnès, Guillot-Noel, Lena, Hannequin, Didier, Lacomblez, Lucette, Golfier, Véronique, Puel, Michèle, Martinaud, Olivier, Deramecourt, Vincent, Rivaud-Pechoux, Sophie, Millecamps, Stéphanie, Vercelletto, Martine, Couratier, Philippe, Sellal, François, Pasquier, Florence, Salachas, François, Thomas-Antérion, Catherine, Didic, Mira, Pariente, Jérémie, Seilhean, Danielle, Ruberg, Merle, Wargon, Isabelle, Blanc, Frédéric, Camu, William, Michel, Bernard-François, Berger, Eric, Sauvée, Mathilde, Thauvin-Robinet, Christel, Mondon, Karl, Tournier-Lasserve, Elisabeth, Goizet, Cyril, Fleury, Marie, Viennet, Gabriel, Verpillat, Patrice, Meininger, Vincent, Duyckaerts, Charles, Dubois, Bruno, Brice, Alexis

“…Frontotemporal dementia (FTD) refers to a disease spectrum including the behavioral variant FTD (bvFTD), primary progressive aphasia (PPA), progressive…”
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The disynaptic group i inhibition between wrist flexor and extensor muscles revisited in humans by WARGON, I, LAMY, J. C, BARET, M, GHANIM, Z, AYMARD, C, PENICAUD, A, KATZ, R

“…The present studies are designed to further characterise the interneuronal pathway mediating the disynaptic reciprocal group I inhibition between flexors and…”
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Aspects cliniques et radiologiques d’une myopathie mitochondriale POLG1 avec syndrome frontal by Wargon, Isabelle, Odile Habert, Marie, Cecile Michon, Claire, Jardel, Claude, Eymard, Bruno

“…Les mutations du gène POLG1 codant la polymerase gamma de l’ADN mitochondrial sont la cause principale de maladies mitochondriales héréditaires cliniquement…”
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Caractéristiques cliniques et évolutifs des syndromes myasthéniques congénitaux avec mutations COLQ by Wargon, Isabelle, Richard, Pascale, Kuntzer, Thierry, Nafissi, Sharifi, Fournier, Emmanuel, Eymard, Bruno, Stojkovic, Tanya

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