Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathies
Masingue, M., Rucheton, B., Bris, C., Romero, N.B., Procaccio, V., Eymard, B
Published in Neuromuscular disorders : NMD (01.12.2022)
Published in Neuromuscular disorders : NMD (01.12.2022)
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Journal Article
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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Journal Article
Strategy for genetic analysis in hereditary neuropathy
Masingue, M., Fernández-Eulate, G., Debs, R., Tard, C., Labeyrie, C., Leonard-Louis, S., Dhaenens, C.-M., Masson, M.A., Latour, P., Stojkovic, T.
Published in Revue neurologique (01.01.2023)
Published in Revue neurologique (01.01.2023)
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Journal Article
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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Journal Article
587P White matter lesions and genetic muscular diseases: an overview
Jaubert, P., Mario, G., Stojkovic, T., Masingue, M.
Published in Neuromuscular disorders : NMD (01.10.2024)
Published in Neuromuscular disorders : NMD (01.10.2024)
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Journal Article
531P The French registry of glycogen storage disease type 3
Masingue, M., Decostre, V., Bello, M., Cao, J. Do, Labrune, P., Laforêt, P.
Published in Neuromuscular disorders : NMD (01.10.2024)
Published in Neuromuscular disorders : NMD (01.10.2024)
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Journal Article
EP.08Highly asymmetrical distribution of muscle wasting correlated with heteroplasmy level in a patient suffering from a mitochondrial myopathy with single deletion of mitochondrial DNA
Masingue, M., Eymard, B., Romero, N., Rucheton, B.
Published in Neuromuscular disorders : NMD (01.10.2019)
Published in Neuromuscular disorders : NMD (01.10.2019)
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Journal Article
P351 Rhabdomyolysis and muscle biopsy outcomes: a single center retrospective cohort
Ferreira, W., Massaro, C., Masingue, M., De Lonlay, P., Laforet, P., Behin, A., Eymard, B., Choumert, A., Mafatti, E., Stojkovic, T., Allenbach, Y., Bassez, G., Evangelista, T.
Published in Neuromuscular disorders : NMD (01.10.2023)
Published in Neuromuscular disorders : NMD (01.10.2023)
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Journal Article
FSHD / OPMD / MYOTONIC DYSTROPHY
Masingue, M., Bisciglia, M., Chanut, A., Labasse, C., Metay, C., Evangelista, T.
Published in Neuromuscular disorders : NMD (01.10.2020)
Published in Neuromuscular disorders : NMD (01.10.2020)
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Journal Article
FSHD / OPMD / MYOTONIC DYSTROPHY: P.223 Specific biopsy findings: a key factor in the diagnosis of OPMD presenting with isolated dropping head syndrome
Masingue, M., Bisciglia, M., Chanut, A., Labasse, C., Metay, C., Evangelista, T.
Published in Neuromuscular disorders : NMD (01.10.2020)
Published in Neuromuscular disorders : NMD (01.10.2020)
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Journal Article
VP429 Impaired skeletal muscle strength in adult patients with laminopathies
Decostre, V., Chikhaoui, C., Vigouroux, C., Behin, A., Bassez, G., Ferreiro, A., Janmaat, S., Masingue, M., Stojkovic, T., Vatier, C., Quiles, R Villar, Roy, S Quijano, Wahbi, K., Eymard, B., Bonne, G., Yaou, R Ben, Hogrel, J.
Published in Neuromuscular disorders : NMD (01.10.2023)
Published in Neuromuscular disorders : NMD (01.10.2023)
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Journal Article
Improved cardiac outcomes by early treatment with angiotensin-converting enzyme inhibitors in becker muscular dystrophy
Motte, L, Stalens, C, Behin, A, Ben Yaou, R, Leturcq, F, Bassez, G, Laforet, P, Fontaine, B, Ederhy, S, Masingue, M, Saadi, M, Leonard Louis, S, Berber, N, Duboc, D, Wahbi, K
Published in European heart journal (12.10.2021)
Published in European heart journal (12.10.2021)
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Journal Article
70P Defining the landscape of TIA1 and SQSTM1 digenic myopathy
Fernández-Eulate, G., Panos-Basterra, P., Theuriet, J., Nadaj-Pakleza, A., Magot, A., Lannes, B., Marcorelles, P., Behin, A., Masingue, M., Caillon, F., Malek, Y., Fenouil, T., Bas, J., Menassa, R., Michel-Calemard, L., Streichenberger, N., Simon, J., Bouhour, F., Evangelista, T., Métay, C., Pegat, A., Stojkovic, T.
Published in Neuromuscular disorders : NMD (01.10.2024)
Published in Neuromuscular disorders : NMD (01.10.2024)
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Journal Article
Congenital myasthenic syndromes in adults: clinical features, diagnosis and long-term prognosis
Theuriet, Julian, Masingue, Marion, Behin, Anthony, Ferreiro, Ana, Bassez, Guillaume, Jaubert, Pauline, Tarabay, Oriana, Fer, Frédéric, Pegat, Antoine, Bouhour, Françoise, Svahn, Juliette, Petiot, Philippe, Jomir, Laurentiu, Chauplannaz, Guy, Cornut-Chauvinc, Catherine, Manel, Véronique, Salort-Campana, Emmanuelle, Attarian, Shahram, Fortanier, Etienne, Verschueren, Annie, Kouton, Ludivine, Camdessanché, Jean-Philippe, Tard, Céline, Magot, Armelle, Péréon, Yann, Noury, Jean-Baptiste, Minot-Myhie, Marie-Christine, Perie, Maud, Taithe, Frederic, Farhat, Yacine, Millet, Anne-Laure, Cintas, Pascal, Solé, Guilhem, Spinazzi, Marco, Esselin, Florence, Renard, Dimitri, Sacconi, Sabrina, Ezaru, Andra, Malfatti, Edoardo, Mallaret, Martial, Magy, Laurent, Diab, Eva, Merle, Philippe, Michaud, Maud, Fournier, Maxime, Pakleza, Aleksandra Nadaj, Chanson, Jean-Baptiste, Lefeuvre, Claire, Laforet, Pascal, Richard, Pascale, Sternberg, Damien, Villar-Quiles, Rocio-Nur, Stojkovic, Tanya, Eymard, Bruno
Published in Brain (London, England : 1878) (04.11.2024)
Published in Brain (London, England : 1878) (04.11.2024)
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Journal Article
P.100Pseudo-increment at repetitive nerve stimulation (Arzel's sign): a new tool for Brody myopathy diagnosis
Masingue, M., Arzel, M., Sternberg, D., Stojkovic, T., Behin, A., Bassez, G., Vicart, S., Péréon, Y., Kuntzer, T., Eymard, B., Fournier, E.
Published in Neuromuscular disorders : NMD (01.10.2019)
Published in Neuromuscular disorders : NMD (01.10.2019)
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Journal Article
Homozygous p.R707W MFN2 mutation is associated with neuropathy, lipomatosis, peripheral lipoatrophy and metabolic alterations
Masingue, M., Vatier, C., Jéru, I., Latour, P., Jardel, C., Laforêt, P., Eymard, B., Vigouroux, C., Stojkovic, T.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
P.172 - Homozygous p.R707W MFN2 mutation is associated with neuropathy, lipomatosis, peripheral lipoatrophy and metabolic alterations
Masingue, M., Vatier, C., Jéru, I., Latour, P., Jardel, C., Laforêt, P., Eymard, B., Vigouroux, C., Stojkovic, T.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article