Antibody‐ and macrophage‐mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlates
Vallat, J.‐M., Mathis, S., Vegezzi, E., Richard, L., Duchesne, M., Gallouedec, G., Corcia, P., Magy, L., Uncini, A., Devaux, J.
Published in European journal of neurology (01.04.2020)
Published in European journal of neurology (01.04.2020)
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IVIg increases interleukin‐11 levels, which in turn contribute to increased platelets, VWF and FVIII in mice and humans
Nguyen, A., Repesse, Y., Ebbo, M., Allenbach, Y., Benveniste, O., Vallat, J. M., Magy, L., Deshayes, S., Maigné, G., Boysson, H., Karnam, A., Delignat, S., Lacroix‐Desmazes, S., Bayry, J., Aouba, A.
Published in Clinical and experimental immunology (01.05.2021)
Published in Clinical and experimental immunology (01.05.2021)
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Real‐life effectiveness 1 year after switching to avalglucosidase alfa in late‐onset Pompe disease patients worsening on alglucosidase alfa therapy: A French cohort study
Tard, Céline, Bouhour, Françoise, Michaud, Maud, Beltran, Stephane, Fournier, Maxime, Demurger, Florence, Lagrange, Emmeline, Nollet, Sylvain, Sacconi, Sabrina, Noury, Jean‐Baptiste, Magot, Armelle, Cintas, Pascal, Renard, Dimitri, Deibener‐Kaminsky, Joëlle, Lefeuvre, Claire, Davion, Jean‐Baptiste, Salort‐Campana, Emmanuelle, Arrassi, Azzeddine, Taouagh, Nadjib, Spinazzi, Marco, Orlikowski, D, Masingue, M, Stojkovic, T, Béhin, A, Garcia, PY, Lallement, F, Bassez, G, Germain, D, Kouton, L, Verschueren, A, Furby, A, Kaminsky, AL, Lacour, A, Praline, J, Sole, G, Duval, F, Bouibede, F, Chapon, F, Minot, MC, Hubert, J, Pereon, Y, Acket, B, Nadaj‐Pakleza, A, Morales, RJ, Esselin, F, Petiot, P, Jaussaud, R, Mohamed, S, Echaniz‐Laguna, YA, Magy, L, Krim, E, Taithe, F, Bedat‐Millet, AL, Toquet, S, Diab, E, Maillet‐Vioud, M, Attarian, Shahram, Laforêt, Pascal
Published in European journal of neurology (01.07.2024)
Published in European journal of neurology (01.07.2024)
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Motor and respiratory decline in patients with late onset Pompe disease after cessation of enzyme replacement therapy during COVID‐19 pandemic
Tard, Céline, Salort‐Campana, Emmanuelle, Michaud, Maud, Spinazzi, Marco, Nadaj Pakleza, Aleksandra, Durr, Hélène, Bouhour, Françoise, Lefeuvre, Claire, Thomas, Romain, Arrassi, Azzeddine, Taouagh, Nadjib, Solé, Guilhem, Laforêt, Pascal, P, Laforêt, D, Orlikowski, G, Bassez, D, Germain, JB, Noury, F, Zagnoli, C, Tard, JB, Davion, E, Salort‐Campana, A, Verschueren, S, Sacconi, A, Furby, A, Lacour, J, Praline, G, Sole, D, Renard, F, Bouibede, M, Fournier, F, Chapon, MC, Minot, M, Spinazzi, J, Hubert, F, Demurger, A, Magot, P, Cintas, A, Nadaj‐Pakleza, F, Bouhour, RJ, Morales, F, Esselin, P, Petiot, R, Jaussaud, S, Pichard, A, Brassier, J, Do‐Cao, F, Feillet, G, Touati, YA, Echaniz‐Laguna, L, Magy, M, Michaud, E, Lagrange, E, Krim, F, Taithe, AL, Bedat‐Millet, S, Nollet, U, Walter‐Louvier, B, Chabrol, M, Tardieu
Published in European journal of neurology (01.04.2022)
Published in European journal of neurology (01.04.2022)
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Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants
Lerat, J., Magdelaine, C., Lunati, A., Dzugan, H., Dejoie, C., Rego, M., Beze Beyrie, P., Bieth, E., Calvas, P., Cintas, P., Delaubrier, A., Demurger, F., Gilbert-Dussardier, B., Goizet, C., Journel, H., Laffargue, F., Magy, L., Taithe, F., Toutain, A., Urtizberea, J.A., Sturtz, F., Lia, A.S.
Published in Journal of the neurological sciences (15.11.2019)
Published in Journal of the neurological sciences (15.11.2019)
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Late-onset Pompe disease in France: molecular features and epidemiology from a nationwide study
Semplicini, Claudio, Letard, Pascaline, De Antonio, Marie, Taouagh, Nadjib, Perniconi, Barbara, Bouhour, Françoise, Echaniz-Laguna, Andoni, Orlikowski, David, Sacconi, Sabrina, Salort-Campana, Emmanuelle, Solé, Guilhem, Zagnoli, Fabien, Hamroun, Dalil, Froissart, Roseline, Caillaud, Catherine, Laforêt, Pascal
Published in Journal of inherited metabolic disease (01.12.2018)
Published in Journal of inherited metabolic disease (01.12.2018)
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Current clinical management of CIDP with immunoglobulins in France: An expert opinion
Cintas, P., Bouhour, F., Cauquil, C., Masingue, M., Tard, C., Sacconi, S., Delmont, E., Choumert, A., Chanson, J.-B., Michaud, M., Solé, G., Cassereau, J., Noury, J.-B., Nicolas, G., Bellance, R., Péréon, Y., Camdessanché, J.-P., Magy, L., Attarian, S.
Published in Revue neurologique (01.10.2023)
Published in Revue neurologique (01.10.2023)
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Transthyretin amyloid polyneuropathy in France: A cross-sectional study with 413 patients and real-world tafamidis meglumine use (2009–2019)
Adams, D., Cintas, P., Solé, G., Tard, C., Labeyrie, C., Echaniz-Laguna, A., Cauquil, C., Pereon, Y., Magy, L., Morales, R. Juntas, Antoine, J.C., Lagrange, E., Petiot, P., Mallaret, M., Francou, B., Guiochon-Mantel, A., Coste, A., Demarcq, O., Geffroy, C., Famelart, V., Rudant, J, Bartoli, M, Donal, E., Lairez, O., Eicher, J.C., Kharoubi, M., Oghina, S., Trochu, J.N., Inamo, J., Habib, G., Roubille, F., Hagège, A., Morio, F., Cariou, E., Adda, J., Slama, M.S., Charron, P., Algalarrondo, V., Damy, T., Attarian, S.
Published in Revue neurologique (01.09.2024)
Published in Revue neurologique (01.09.2024)
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Phenotypic spectrum of Charcot−Marie−Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patients
Guimarães‐Costa, R., Iancu Ferfoglia, R., Leonard‐Louis, S., Ziegler, F., Magy, L., Fournier, E., Dubourg, O., Bouche, P., Maisonobe, T., Lacour, A., Moerman, A., Latour, P., Stojkovic, T.
Published in European journal of neurology (01.03.2017)
Published in European journal of neurology (01.03.2017)
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Journal Article
Classifications of neurogenetic diseases: An increasingly complex problem
Vallat, J.-M., Goizet, C., Tazir, M., Couratier, P., Magy, L., Mathis, S.
Published in Revue neurologique (01.06.2016)
Published in Revue neurologique (01.06.2016)
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Journal Article
Motor neuronopathy in Chediak–Higashi syndrome
Mathis, S, Cintas, P, de Saint-Basile, G, Magy, L, Funalot, B, Vallat, J.-M
Published in Journal of the neurological sciences (15.09.2014)
Published in Journal of the neurological sciences (15.09.2014)
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Journal Article
The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2
Klünemann, H H, Ridha, B H, Magy, L, Wherrett, J R, Hemelsoet, D M, Keen, R W, De Bleecker, J L, Rossor, M N, Marienhagen, J, Klein, H E, Peltonen, L, Paloneva, J
Published in Neurology (10.05.2005)
Published in Neurology (10.05.2005)
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Journal Article
Muscular weakness and weight loss in à 44 year-old man
Mas, R, Magy, L, Jésus, P, Ly, K, Archambeaud, F, Gondran, G
Published in La revue de medecine interne (01.12.2021)
Published in La revue de medecine interne (01.12.2021)
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Journal Article
Actualités des neuropathies dysimmunitaires (hors traitement)
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Conference Proceeding
POEMS syndrome with prominent acute axonal lesions
Mathis, S, Magy, L, Kaboré, R, Faugeras, F, Richard, L, Vallat, J.-M
Published in Journal of the neurological sciences (15.02.2012)
Published in Journal of the neurological sciences (15.02.2012)
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