Genetic mosaicism in Systemic Auto-Inflammatory Diseases: A review of the literature von Parentelli, A-S, Boursier, G, Cuisset, L, Georgin-Lavialle, S

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Is gene panel sequencing more efficient than clinical‐based gene sequencing to diagnose autoinflammatory diseases? A randomized study von Rama, M., Mura, T., Kone‐Paut, I., Boursier, G., Aouinti, S., Touitou, I., Sarrabay, G.

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PASS: a rare syndrome within the autoinflammatory diseases that still lacks a genetic marker von Schwob, E., Bessis, D., Boursier, G., Kottler, D., Guillot, B., Lerisson, M., Girard, C.

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Monogenic auto-inflammatory diseases associated with actinopathies: A review of the literature von Mertz, P, Hentgen, V, Boursier, G, Delon, J, Georgin-Lavialle, S

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A20 haploinsufficiency: what do clinicians need to know? von Elhani, I, Aouba, A, Riller, Q, Vergneault, H, Boursier, G, Rieux-Laucat, F, Hentgen, V, Georgin-Lavialle, S

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French protocol for the diagnosis and management of familial Mediterranean fever von Georgin-Lavialle, S., Savey, L., Cuisset, L., Boursier, G., Boffa, J.-J., Delplanque, M., Bourguiba, R., Monfort, J.-B., Touitou, I., Grateau, G., Kone-Paut, I., Hentgen, V.

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Wiedemann‐Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases von Baer, S., Afenjar, A., Smol, T., Piton, A., Gérard, B., Alembik, Y., Bienvenu, T., Boursier, G., Boute, O., Colson, C., Cordier, M.‐P., Cormier‐Daire, V., Delobel, B., Doco‐Fenzy, M., Duban‐Bedu, B., Fradin, M., Geneviève, D., Goldenberg, A., Grelet, M., Haye, D., Heron, D., Isidor, B., Keren, B., Lacombe, D., Lèbre, A.‐S., Lesca, G., Masurel, A., Mathieu‐Dramard, M., Nava, C., Pasquier, L., Petit, A., Philip, N., Piard, J., Rondeau, S., Saugier‐Veber, P., Sukno, S., Thevenon, J., Van‐Gils, J., Vincent‐Delorme, C., Willems, M., Schaefer, E., Morin, G.

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European young scientists: Training and career von Boursier, G.

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Case Report: Persistency Pneumococcal Polysaccharide in Cerebrospinal Fluid During a Post Pneumococcal Chronic Aseptic Meningitis: Coincidental or (Auto-)Inflammatory Embers von Ladeveze, Manon, Dumont, Yann, Boursier, G, Batteux, Frederic, Mahe, Perrine, Bensimon Borrull, Aurelie, Sarrabay, Guillaume, Bollore, Karine, Tuaillon, Edouard, Godreuil, Sylvain, Jeziorski, Eric

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Revue de la littérature sur les syndromes auto-inflammatoires monogéniques liés aux actinopathies von Mertz, P., Hentgen, V., Boursier, G., Delon, J., Georgin-Lavialle, S.

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Current landscape of monogenic autoinflammatory actinopathies: A literature review von Mertz, P., Hentgen, V., Boursier, G., Delon, J., Georgin-Lavialle, S.

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Further characterization of clinical and laboratory features in VEXAS syndrome: large‐scale analysis of a multicentre case series of 116 French patients von Georgin‐Lavialle, S., Terrier, B., Guedon, A.F., Heiblig, M., Comont, T., Lazaro, E., Lacombe, V., Terriou, L., Ardois, S., Bouaziz, J.‐D., Mathian, A., Le Guenno, G., Aouba, A., Outh, R., Meyer, A., Roux‐Sauvat, M., Ebbo, M., Zhao, L.P., Bigot, A., Jamilloux, Y., Guillotin, V., Flamarion, E., Henneton, P., Vial, G., Jachiet, V., Rossignol, J., Vinzio, S., Weitten, T., Vinit, J., Deligny, C., Humbert, S., Samson, M., Magy‐Bertrand, N., Moulinet, T., Bourguiba, R., Hanslik, T., Bachmeyer, C., Sebert, M., Kostine, M., Bienvenu, B., Biscay, P., Liozon, E., Sailler, L., Chasset, F., Audemard‐Verger, A., Duroyon, E., Sarrabay, G., Borlot, F., Dieval, C., Cluzeau, T., Marianetti, P., Lobbes, H., Boursier, G., Gerfaud‐Valentin, M., Jeannel, J., Servettaz, A., Audia, S., Larue, M., Henriot, B., Faucher, B., Graveleau, J., Sainte Marie, B., Galland, J., Bouillet, L., Arnaud, C., Ades, L., Carrat, F., Hirsch, P., Fenaux, P., Fain, O., Sujobert, P., Kosmider, O., Mekinian, A.

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Strategy for anti-aquaporin-4 auto-antibody identification and quantification using a new cell-based assay von De Vidi, I, Boursier, G, Delouche, N, Portalès, P, Cadars, E, Bouthier, M, Mettling, C, Lin, Y.L, Thouvenot, E, Carlander, B, Camu, W, Antel, J.P, Bar-Or, A, Zephir, H, Vermersch, P, De Seze, J, Corbeau, P, Eliaou, J.F, Vincent, T

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Clinical and pathological features of cutaneous manifestations in VEXAS syndrome: A multicenter retrospective study of 59 cases von Zakine, Ève, Papageorgiou, Loula, Bourguiba, Rim, Mekinian, Arsène, Terrier, Benjamin, Kosmider, Olivier, Hirsch, Pierre, Jachiet, Marie, Audia, Sylvain, Ardois, Samuel, Adélaïde, Léopold, Bigot, Adrien, Duriez, Paul, Emile, Jean-François, Lazaro, Estibaliz, Fayard, Damien, Galland, Joris, Hié, Miguel, Humbert, Sébastien, Jean, Alexis, Kostine, Marie, Lacombe, Valentin, Le Guenno, Guillaume, Lobbes, Hervé, Magy-Bertrand, Nadine, Marianetti-Guingel, Paola, Mathian, Alexis, Outh, Rodérau, Saillard, Clémence, Samson, Maxime, Vial, Guillaume, Bouaziz, Jean-David, Moguelet, Philippe, Chasset, François, Amoura, Z., Aouba, A., Arnaud, C., Audemard-Verger, A., Bachmeyer, C., Bienvenu, B., Biscay, P., Borlot, F., Bouillet, L., Boursier, G., Carrat, F., Cluzeau, T., Comont, T., Constantin, A., de Sainte Marie, B., Deligny, C., Dieval, C., Duroyon, E., Ebbo, M., Fain, O., Faucher, B., Fenaux, P., Georgin-Lavialle, S., Gerfaud-Valentin, M., Graveleau, J., Guedon, A.F., Hanslik, T., Heiblig, M., Jachiet, V., Jamilloux, Y., Jeannel, J., Larue, M., Le Pelletier, F., Liozon, E., Meyer, A., Moulinet, T., Pha, M., Rossignol, J., Roux, M., Roux-Sauvat, M., Sailler, L., Sarrabay, G., Sebert, M., Servettaz, A., Sujobert, P., Terriou, L., Vinit, J., Vinzio, S., Weitten, T., Zhao, L.P.

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First report of MEFV gene duplication in a patient with familial Mediterranean fever von Mechin, Déborah, Durinikova, Anna, Boursier, Guilaine, André, Marc, Touitou, Isabelle, Sarrabay, Guillaume

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M133 An approach for determining allowable between reagent lot variation von Van Schrojenstein Lantman, M., Can Çubukçu, H., Boursier, G., Panteghini, M., Bernabeu-Andreu, F.A., Milinkovic, N., Mesko Brguljan, P., Linko, S., Brugnon, D., O'Kelly, R., Kroupis, C., Lohmander, M., Šprongl, L., Vanstapel, F., Thelen, M.

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Mosaïcisme génétique dans les maladies auto-inflammatoires : revue de la littérature von Parentelli, A.-S., Boursier, G., Cuisset, L., Georgin-Lavialle, S.

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Further characterization of clinical and laboratory features in VEXAS syndrome: large‐scale analysis of a multicentre case series of 116 French patients von Georgin-Lavialle, S., Terrier, B., Guedon, A.F., Heiblig, M., Comont, T., Lazaro, E., Lacombe, V., Terriou, L., Ardois, S., Bouaziz, J.‐d., Mathian, A., Le Guenno, G., Aouba, A., Outh, R., Meyer, A., Roux-Sauvat, M., Ebbo, M., Zhao, L.P., Bigot, A., Jamilloux, Y., Guillotin, V., Flamarion, E., Henneton, P., Vial, G., Jachiet, V., Rossignol, J., Vinzio, S., Weitten, T., Vinit, J., Deligny, C., Humbert, S., Samson, M., Magy-Bertrand, N., Moulinet, T., Bourguiba, R., Hanslik, T., Bachmeyer, C., Sebert, M., Kostine, M., Bienvenu, B., Biscay, P., Liozon, E., Sailler, L., Chasset, F., Audemard-Verger, A., Duroyon, E., Sarrabay, G., Borlot, F., Dieval, C., Cluzeau, T., Marianetti, P., Lobbes, H., Boursier, G., Gerfaud-Valentin, M., Jeannel, J., Servettaz, A., Audia, S., Larue, M., Henriot, B., Faucher, B., Graveleau, J., de Sainte Marie, B., Galland, J., Bouillet, L., Arnaud, C., Ades, L., Carrat, F., Hirsch, P., Fenaux, P., Fain, O., Sujobert, P., Kosmider, O., Mekinian, A.

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Diagnostic et présentation clinique de l’haploinsuffisance de A20 en 2023 von Elhani, I., Riller, Q., Boursier, G., Rieux-Laucat, F., Hentgen, V., Georgin-Lavialle, S.

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L’haploinsuffisance de A20 : que doit connaître le clinicien? von Elhani, I., Aouba, A., Riller, Q., Vergneault, H., Boursier, G., Rieux-Laucat, F., Hentgen, V., Georgin-Lavialle, S.

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