Neurological outcomes in immune checkpoint inhibitor-related neurotoxicity by Farina, Antonio, Birzu, Cristina, Elsensohn, Mad-Hélénie, Picca, Alberto, Muñiz-Castrillo, Sergio, Vogrig, Alberto, Villagrán-García, Macarena, Ciano-Petersen, Nicolás Lundahl, Massacesi, Luca, Hervier, Baptiste, Guégan, Sarah, Kramkimel, Nora, Vano, Yann, Salem, Joe Elie, Allenbach, Yves, Maisonobe, Thierry, Assaad, Souad, Maureille, Aurélien, Devic, Perrine, Weiss, Nicolas, Pegat, Antoine, Maucort-Boulch, Delphine, Ricard, Damien, Honnorat, Jérôme, Psimaras, Dimitri, Joubert, Bastien

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Apport du SUDOSCAN dans le diagnostic du syndrome du canal carpien by Pegat, Antoine, Pegat, Benoit, Jomir, Laurent, Vial, Christophe, Bouhour, Françoise

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Cas clinique 2 : cas d’une atteinte multitronculaire dans un contexte infectieux by Brenière, Céline, Pegat, Antoine, Svahn, Juliette, Bernard, Emilien, Petiot, Philippe, Bouhour, Françoise

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Atteinte des conductances cutanées électrochimiques au sudoscan dans le cadre d’un syndrome de Lambert Eaton associé à une myasthénie auto-immune by Pegat, Antoine, Jomir, Laurent, Bouhour, Françoise, Jeannin-Mayer, Sophie

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Plasmocytome multiple intracrânien et digestif by Drouet, Alain, Defrance, Julie, Pegat, Antoine, Guilloton, Laurent

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Myelitis Migrans by Jaulent, Paul, Pegat, Antoine, Grosset-Janin, Clara, Durand-Dubief, Françoise, Marignier, Romain, Vukusic, Sandra

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Neuropathie optique infiltrative bilatérale révélatrice d’une maladie de Waldenström by Agard, Emilie, Pegat, Antoine, Vanquaethem, Hélène, El Chehab, Hussam, Dot, Corinne, Guilloton, Laurent

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Anémie néonatale chez une enfant née après une exposition maternelle au natalizumab durant toute la grossesse by Guilloton, Laurent, Pegat, Antoine, Defrance, Julie, Quesnel, Laetitia, Barral, Gérard, Drouet, Alain

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Space girl by Pegat, Antoine, Schmitt, Alexandre, Plouzennec, Yann, Drouet, Alain, Quesnel, Laetitia, Guilloton, Laurent

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Juvenile amyotrophic lateral sclerosis associated with biallelic c.757delG mutation of sorbitol dehydrogenase gene by Bernard, Emilien, Pegat, Antoine, Vallet, Anne-Evelyne, Leblanc, Pascal, Lumbroso, Serge, Mouzat, Kevin, Latour, Philippe

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Amyotrophic lateral sclerosis associated with a pathological expansion in the ATXN7 gene by Cluse, Florent, Bernard, Emilien, Strubi-Vuillaume, Isabelle, Devos, David, Mouzat, Kevin, Lumbroso, Serge, Froment Tilikete, Caroline, Thobois, StÉphane, Pegat, Antoine

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Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy-Case Report by Pegat, Antoine, Streichenberger, Nathalie, Lacoste, Nicolas, Hermier, Marc, Menassa, Rita, Coudert, Laurent, Theuriet, Julian, Froissart, Roseline, Terrone, Sophie, Bouhour, Francoise, Michel-Calemard, Laurence, Schaeffer, Laurent, Jacquier, Arnaud

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Phenoconversion from Spastic Paraplegia to ALS/FTD Associated with CYP7B1 Compound Heterozygous Mutations by Theuriet, Julian, Pegat, Antoine, Leblanc, Pascal, Vukusic, Sandra, Cazeneuve, Cécile, Millecamps, Stéphanie, Banneau, Guillaume, Guillaud-Bataille, Marine, Bernard, Emilien

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