TTC7A mutation must be considered in patients with repeated intestinal atresia associated with early inflammatory bowel disease: Two new case reports and a literature review von Fayard, J., Collardeau, S., Bertrand, Y., Cordier, M.-P., Malcus, C., Dubois, R., Mure, P.-Y., de Saint Basile, G., Louazon, T., Rohmer, B., Lachaux, A., Duclaux, R., Peretti, N.

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NATURALLY OCCURRING PRIMARY DEFICIENCIES OF THE IMMUNE SYSTEM von Fischer, A, Cavazzana-Calvo, M, Basile, G. De Saint, DeVillartay, J. P, Di Santo, J. P, Hivroz, C, Rieux-Laucat, F, Le Deist, F

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CNS involvement at the onset of primary hemophagocytic lymphohistiocytosis von DEIVA, K, MAHLAOUI, N, BEAUDONNET, F, DE SAINT BASILE, G, CARIDADE, G, MOSHOUS, D, MIKAELOFF, Y, BLANCHE, S, FISCHER, A, TARDIEU, M

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Ichthyosis as the dermatological phenotype associated with TTC7A mutations von Leclerc-Mercier, S., Lemoine, R., Bigorgne, A.E., Sepulveda, F., Leveau, C., Fischer, A., Mahlaoui, N., Hadj-Rabia, S., de Saint Basile, G.

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An atypical case of X-linked lymphoproliferative disease revealed as a late cerebral lymphoma von Hervier, B, Latour, S, Loussouarn, D, Rimbert, M, De-Saint-Basile, G, Picard, C, Hamidou, M

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CD40-CD40L Independent Ig Gene Hypermutation Suggests a Second B Cell Diversification Pathway in Humans von Weller, Sandra, Faili, Ahmad, Garcia, Corinne, Braun, Moritz C., Le Deist, Françoise, Geneviève de Saint Basile, Hermine, Olivier, Fischer, Alain, Reynaud, Claude-Agnès, Weill, Jean-Claude

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Severe combined immunodeficiency: A retrospective single-center study of clinical presentation and outcome in 117 patients von Stephan, J.L., Vlekova, V., Deist, F. Le, Blanche, S., Donadieu, J., Saint-Basile, G. De, Durandy, A., Griscelli, C., Fischer, A.

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Motor neuronopathy in Chediak–Higashi syndrome von Mathis, S, Cintas, P, de Saint-Basile, G, Magy, L, Funalot, B, Vallat, J.-M

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Successful treatment of Griscelli syndrome with unrelated donor allogeneic hematopoietic stem cell transplantation von Aricò, M, Zecca, M, Santoro, N, Caselli, D, Maccario, R, Danesino, C, de Saint Basile, G, Locatelli, F

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Rab27a controls HIV-1 assembly by regulating plasma membrane levels of phosphatidylinositol 4,5-bisphosphate von Gerber, P. Pereyra, Cabrini, M., Jancic, C., Paoletti, L., Banchio, C., von Bilderling, C., Sigaut, L., Pietrasanta, L., Duette, G., Freed, E, de Saint Basile, G., Moita, C. Ferreira, Moita, L. Ferreira, Amigorena, S., Benaroch, P., Geffner, J., Ostrowski, Matias

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Familial haemophagocytosis lymphohisticytosis type 3: A case report von Kamoun, F., Hsairi, M., Grandin, V., Ben Ameur, S., De Saint Basile, G., Hachicha, M.

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Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene von Griscelli, Claude, Pastural, Elodie, Jabado, Nada, Fischer, Alain, Basile, Geneviève de Saint, Barrat, Franck J, Dufourcq-Lagelouse, Rémi, Sanal, Ozden, Seger, Reinhard, Certain, Stéphanie

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Lymphome T sous-cutané de type panniculite de la face : absence de perte d’expression de TIM3 et réponse complète à l’association corticothérapie–méthotrexate von Marcé, D., Laurent, C., Pottier, C., Kervarrec, T., De Muret, A., De Saint Basile, G., Samimi, M.

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The role of cytotoxicity in lymphocyte homeostasis von de Saint Basile, Geneviève, Fischer, Alain

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CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM von DiSanto, J. P, Bonnefoy, J. Y, Gauchatt, J. F, Fischer, A, Saint Basile, G. de

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Hematopoietic Stem Cell Transplantation in Hemophagocytic Lymphohistiocytosis: A Single-Center Report of 48 Patients von Ouachee-Chardin, Marie, Elie, Caroline, de Saint Basile, Genevieve, Le Deist, Francoise, Mahlaoui, Nizar, Picard, Capucine, Neven, Benedicte, Casanova, Jean-Laurent, Tardieu, Marc, Cavazzana-Calvo, Marina, Blanche, Stephane, Fischer, Alain

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Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes von Feldmann, Jérôme, Prieur, Anne-Marie, Quartier, Pierre, Berquin, Patrick, Certain, Stéphanie, Cortis, Elisabetta, Teillac-Hamel, Dominique, Fischer, Alain, Basile, Geneviève de Saint

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Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product von Pasquier, Benoit, Yin, Luo, Fondanèche, Marie-Claude, Relouzat, Francis, Bloch-Queyrat, Coralie, Lambert, Nathalie, Fischer, Alain, de Saint-Basile, Geneviève, Latour, Sylvain

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Signaling lymphocytic activation molecule (SLAM) regulates T cellular cytotoxicity von Henning, Golo, Kraft, Michael S., Derfuss, Tobias, Pirzer, Rainer, Saint‐Basile, Geneviève de, Aversa, Gregorio, Fleckenstein, Bernhard, Meinl, Edgar

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Functional common gamma chain is not required for mast cell proliferation and survival von Chapdelaine, H, Canioni, D, De Saint-Basile, G, Hermine, O, Fischer, A

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