A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions
Chevessier, Frédéric, Girard, Emmanuelle, Molgó, Jordi, Bartling, Sönke, Koenig, Jeanine, Hantaï, Daniel, Witzemann, Veit
Published in Human molecular genetics (15.11.2008)
Published in Human molecular genetics (15.11.2008)
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G.P.44
Eymard, B, Ghorab, K, Laforet, P, Chevessier, F, Vallat, J, Hantai, D, Romero, N, Böhm, J, Laporte, J
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience
Eymard, B, Stojkovic, T, Sternberg, D, Richard, P, Nicole, S, Fournier, E, Béhin, A, Laforêt, P, Servais, L, Romero, N, Fardeau, M, Hantaï, D
Published in Revue neurologique (01.02.2013)
Published in Revue neurologique (01.02.2013)
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Novel subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome
Outteryck, O, Richard, P, Lacour, A, Fournier, E, Zephir, H, Gaudon, K, Eymard, B, Hantai, D, Vermersch, P, Stojkovic, T
Published in Journal of neurology, neurosurgery and psychiatry (09.12.2008)
Published in Journal of neurology, neurosurgery and psychiatry (09.12.2008)
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Novel ϵ subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome
Outteryck, O, Richard, P, Lacour, A, Fournier, E, Zéphir, H, Gaudon, K, Eymard, B, Hantaï, D, Vermersch, P, Stojkovic, T
Published in Journal of neurology, neurosurgery and psychiatry (01.04.2009)
Published in Journal of neurology, neurosurgery and psychiatry (01.04.2009)
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Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations
Wargon, I, Richard, P, Kuntzer, T, Sternberg, D, Nafissi, S, Gaudon, K, Lebail, A, Bauche, S, Hantaï, D, Fournier, E, Eymard, B, Stojkovic, T
Published in Neuromuscular disorders : NMD (01.04.2012)
Published in Neuromuscular disorders : NMD (01.04.2012)
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G.P.11.10 Partial genomic deletions of RAPSN account for 15% of congenital myasthenic syndrome after negative DNA sequencing
Richard, P, Gaudon, K, Pénisson-Besnier, I, Chabrol, B, Bouhour, F, Vial, C, Ammar, A. Ben, Bauché, S, Eymard, B, Hantai, D
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
Ben Ammar, A., Petit, F., Alexandri, N., Gaudon, K., Bauché, S., Rouche, A., Gras, D., Fournier, E., Koenig, J., Stojkovic, T., Lacour, A., Petiot, P., Zagnoli, F., Viollet, L., Pellegrini, N., Orlikowski, D., Lazaro, L., Ferrer, X., Stoltenburg, G., Paturneau-Jouas, M., Hentati, F., Fardeau, M., Sternberg, D., Hantaï, D., Richard, P., Eymard, B.
Published in Journal of neurology (01.05.2010)
Published in Journal of neurology (01.05.2010)
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Developmental Regulation of Amyloid Precursor Protein at the Neuromuscular Junction in Mouse Skeletal Muscle
Akaaboune, Mohammed, Allinquant, Bernadette, Farza, Hend, Roy, Karine, Magoul, Rabia, Fiszman, Marc, Festoff, Barry W., Hantaı̈, Daniel
Published in Molecular and cellular neuroscience (01.04.2000)
Published in Molecular and cellular neuroscience (01.04.2000)
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Experimental and pathological changes of the neuromuscular junction
Koenig, J, Bauché, S, Ben Ammar, A, Nicolle, D, Rigoard, P, Eymard, B, Hantaï, D
Published in Neuro-chirurgie (01.03.2009)
Published in Neuro-chirurgie (01.03.2009)
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Structural and molecular organization, development and maturation of the neuromuscular junction
Rigoard, P, Buffenoir, K, Bauche, S, Giot, J-P, Koenig, J, Hantaï, D, Lapierre, F, Wager, M
Published in Neuro-chirurgie (01.03.2009)
Published in Neuro-chirurgie (01.03.2009)
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Thrombin Receptor Induction by Injury-Related Factors in Human Skeletal Muscle Cells
Mbebi, Corinne, Rohn, Troy, Doyennette, Marie-Agnès, Chevessier, Frédéric, Jandrot-Perrus, Martine, Hantaı̈, Daniel, Verdière-Sahuqué, Martine
Published in Experimental cell research (01.02.2001)
Published in Experimental cell research (01.02.2001)
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Tools and techniques dedicated to neuromuscular junction observation
Rigoard, P, Buffenoir, K, Bauche, S, Fares, M, Koenig, J, Hantaï, D, Giot, J-P, Seguin, F, Huze, C, Schaeffer, L, Maixent, J-M
Published in Neuro-chirurgie (01.03.2009)
Published in Neuro-chirurgie (01.03.2009)
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Morphological study of CNS lesions and the consequences on rat neuromuscular junction and peripheral nerve using confocal laser scanning microscopy and Koelle's technique
Rigoard, P, Buffenoir, K, Chaillou, M, Fares, M, Da Costa, L, Boildieu, N, Seguin, F, Lapierre, F, Maixent, J-M, Bauche, S, Koenig, J, Hantaï, D
Published in Neuro-chirurgie (01.03.2009)
Published in Neuro-chirurgie (01.03.2009)
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The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
Richard, P, Gaudon, K, Haddad, H, Ammar, A Ben, Genin, E, Bauché, S, Paturneau-Jouas, M, Müller, J S, Lochmüller, H, Grid, D, Hamri, A, Nouioua, S, Tazir, M, Mayer, M, Desnuelle, C, Barois, A, Chabrol, B, Pouget, J, Koenig, J, Gouider-Khouja, N, Hentati, F, Eymard, B, Hantaï, D
Published in Neurology (09.12.2008)
Published in Neurology (09.12.2008)
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Expression of the thrombin receptor (PAR-1) during rat skeletal muscle differentiation
Chevessier, Frédéric, Hantaï, Daniel, Verdière-Sahuqué, Martine
Published in Journal of cellular physiology (01.11.2001)
Published in Journal of cellular physiology (01.11.2001)
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Tubular aggregates are from whole sarcoplasmic reticulum origin: alterations in calcium binding protein expression in mouse skeletal muscle during aging
Chevessier, F, Marty, I, Paturneau-Jouas, M, Hantaı̈, D, Verdière-Sahuqué, M
Published in Neuromuscular disorders : NMD (01.03.2004)
Published in Neuromuscular disorders : NMD (01.03.2004)
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