Expanding spectrum, intrafamilial diversity, and therapeutic challenges from 15 patients with heterozygous CARD11-associated diseases: A single center experience von Urdinez, Luciano, Erra, Lorenzo, Palma, Alejandro M, Mercogliano, María F, Fernandez, Julieta Belén, Prieto, Emma, Goris, Verónica, Bernasconi, Andrea, Sanz, Marianela, Villa, Mariana, Bouso, Carolina, Caputi, Lucia, Quesada, Belen, Solis, Daniel, Aguirre Bruzzo, Anabel, Katsicas, Maria Martha, Galluzzo, Laura, Weyersberg, Christian, Bocian, Marcela, Bujan, Maria Marta, Oleastro, Matías, Almejun, María B, Danielian, Silvia

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Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence von Sbihi, Zineb, Tanita, Kay, Bachelet, Camille, Bole, Christine, Jabot-Hanin, Fabienne, Tores, Frederic, Le Loch, Marc, Khodr, Radi, Hoshino, Akihiro, Lenoir, Christelle, Oleastro, Matias, Villa, Mariana, Spossito, Lucia, Prieto, Emma, Danielian, Silvia, Brunet, Erika, Picard, Capucine, Taga, Takashi, Abdrabou, Shimaa Said Mohamed Ali, Isoda, Takeshi, Yamada, Masafumi, Palma, Alejandro, Kanegane, Hirokazu, Latour, Sylvain

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Germline hypomorphic CARD11 mutations in severe atopic disease von Ma, Chi A, Stinson, Jeffrey R, Zhang, Yuan, Abbott, Jordan K, Weinreich, Michael A, Hauk, Pia J, Reynolds, Paul R, Lyons, Jonathan J, Nelson, Celeste G, Ruffo, Elisa, Dorjbal, Batsukh, Glauzy, Salomé, Yamakawa, Natsuko, Arjunaraja, Swadhinya, Voss, Kelsey, Stoddard, Jennifer, Niemela, Julie, Zhang, Yu, Rosenzweig, Sergio D, McElwee, Joshua J, DiMaggio, Thomas, Matthews, Helen F, Jones, Nina, Stone, Kelly D, Palma, Alejandro, Oleastro, Matías, Prieto, Emma, Bernasconi, Andrea R, Dubra, Geronimo, Danielian, Silvia, Zaiat, Jonathan, Marti, Marcelo A, Kim, Brian, Cooper, Megan A, Romberg, Neil, Meffre, Eric, Gelfand, Erwin W, Snow, Andrew L, Milner, Joshua D

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Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency von Rosain, Jérémie, Bernasconi, Andrea, Prieto, Emma, Caputi, Lucia, Le Voyer, Tom, Buda, Guadalupe, Marti, Marcelo, Bohlen, Jonathan, Neehus, Anna-Lena, Castaños, Claudio, Gallagher, Rosario, Dorgham, Karim, Oleastro, Matias, Perez, Laura, Danielian, Silvia, Dipierri, Jose Edgardo, Casanova, Jean-Laurent, Bustamante, Jacinta, Villa, Mariana

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T and NK cell functionality in a patient harboring heterozygous novel BCL11B p.Asp632fsAla91 and STX11 p.R129P mutations von Erra, Lorenzo, Colado, Ana, Brunello, Franco Gino, Prieto, Emma, Goris, Verónica, Villa, Mariana, Oleastro, Matías, Martí, Marcelo, Pozner, Roberto Gabriel, Borge, Mercedes, Almejun, María Belén

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CD62‐L down‐regulation after L18‐MDP stimulation as a complementary flow cytometry functional assay for the diagnosis of XIAP deficiency von Rizzo, Agustín D., Sanz, Marianela, Roffe, Georgina, Sajaroff, Elisa O., Prado, Damian A., Prieto, Emma, Goris, Verónica, Rossi, Jorge G., Bernasconi, Andrea R.

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Cancer Prevalence in Children with Inborn Errors of Immunity: Report from a Single Institution von Mitchell, María Raquel, Urdinez, Luciano, Bernasconi, Andrea R., Danielian, Silvia, Katsikas, María Martha, Sajaroff, Elisa O., Roffé, Georgina, Villa, Nélida M., Galluzzo, Laura, Sanz, Marianela, Palma, Alejandro M., Bouso, Carolina, Prieto, Emma, Goris, Verónica, Yancoski, Judith, Rosenzweig, Sergio D., Oleastro, Matías, Rosé, Adriana, Cacciavillano, Walter, Felizzia, Guido, Guitter, Myriam, Sánchez La Rosa, Cristian, Ríos, Mailén, Zubizarreta, Pedro, Felice, María Sara, Rossi, Jorge G.

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Late diagnosis of WHIM sydrome von Paolini, María V, Danielian, Silvia, Prieto, Emma, Tami, María Fernanda, Oleastro, Matías M, Fernández Romero, Diego S

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Germline hypomorphic, dominant interfering CARD11 mutations drive severe atopic disease von Snow, Andrew L, Ma, Chi, Stinson, Jeffrey R, Zhang, Yuan, Abbott, Jordan K, Weinrich, Michael A, Hauk, Pia J, Reynolds, Paul R, Lyons, Jonathan J, Nelson, Celeste G, Ruffo, Elisa, Dorjbal, Batsukh, Glauzy, Salome, Stoddard, Jennifer, Niemela, Julie, Rosenzweig, Sergio D, McElwee, Joshua J, DiMaggio, Thomas, Stone, Kelly D, Palma, Alejandro, Oleastro, Matias, Prieto, Emma, Bernasconi, Andrea R, Dubra, Geronimo, Danielian, Silvia, Zaiat, Jonathan, Marti, Marcello A, Kim, Brian S, Cooper, Megan A, Romberg, Neil, Meffre, Eric, Gelfand, Erwin W, Milner, Joshua D.

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Erratum: Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease von Ma, Chi A, Stinson, Jeffrey R, Zhang, Yuan, Abbott, Jordan K, Weinreich, Michael A, Hauk, Pia J, Reynolds, Paul R, Lyons, Jonathan J, Nelson, Celeste G, Ruffo, Elisa, Dorjbal, Batsukh, Glauzy, Salomé, Yamakawa, Natsuko, Arjunaraja, Swadhinya, Voss, Kelsey, Stoddard, Jennifer, Niemela, Julie, Zhang, Yu, Rosenzweig, Sergio D, McElwee, Joshua J, DiMaggio, Thomas, Matthews, Helen F, Jones, Nina, Stone, Kelly D, Palma, Alejandro, Oleastro, Matías, Prieto, Emma, Bernasconi, Andrea R, Dubra, Geronimo, Danielian, Silvia, Zaiat, Jonathan, Marti, Marcelo A, Kim, Brian, Cooper, Megan A, Romberg, Neil D, Meffre, Eric, Gelfand, Erwin W, Snow, Andrew L, Milner, Joshua D

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Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease von Ma, Chi A, Stinson, Jeffrey R, Zhang, Yuan, Abbott, Jordan K, Weinreich, Michael A, Hauk, Pia J, Reynolds, Paul R, Lyons, Jonathan J, Nelson, Celeste G, Ruffo, Elisa, Dorjbal, Batsukh, Glauzy, Salomé, Yamakawa, Natsuko, Arjunaraja, Swadhinya, Voss, Kelsey, Stoddard, Jennifer, Niemela, Julie, Zhang, Yu, Rosenzweig, Sergio D, McElwee, Joshua J, DiMaggio, Thomas, Matthews, Helen F, Jones, Nina, Stone, Kelly D, Palma, Alejandro, Oleastro, Matías, Prieto, Emma, Bernasconi, Andrea R, Dubra, Geronimo, Danielian, Silvia, Zaiat, Jonathan, Marti, Marcelo A, Kim, Brian, Cooper, Megan A, Romberg, Neil D, Meffre, Eric, Gelfand, Erwin W, Snow, Andrew L, Milner, Joshua D

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Correction: Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease von Ma, Chi A, Stinson, Jeffrey R, Zhang, Yuan, Abbott, Jordan K, Weinreich, Michael A, Hauk, Pia J, Reynolds, Paul R, Lyons, Jonathan J, Nelson, Celeste G, Ruffo, Elisa, Dorjbal, Batsukh, Glauzy, Salomé, Yamakawa, Natsuko, Arjunaraja, Swadhinya, Voss, Kelsey, Stoddard, Jennifer, Niemela, Julie, Zhang, Yu, Rosenzweig, Sergio D, McElwee, Joshua J, DiMaggio, Thomas, Matthews, Helen F, Jones, Nina, Stone, Kelly D, Palma, Alejandro, Oleastro, Matías, Prieto, Emma, Bernasconi, Andrea R, Dubra, Geronimo, Danielian, Silvia, Zaiat, Jonathan, Marti, Marcelo A, Kim, Brian, Cooper, Megan A, Romberg, Neil D, Meffre, Eric, Gelfand, Erwin W, Snow, Andrew L, Milner, Joshua D

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Clinical and Molecular Analysis of 49 Patients With X-linked Agammaglobulinemia From A Single Center in Argentina von Basile, Natalia, Danielian, Silvia, Oleastro, Matias, Rosenzweig, Sergio, Prieto, Emma, Rossi, Jorge, Roy, Adriana, Zelazko, Marta

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The Effect of Diet on Gonadal Development of the Smooth Venus ClamCallista chione (Mollusca: Bivalvia) von Martinez-Pita, Ines, Sanchez-Lazo, Clara, Prieto, Emma, Moreno, Oscar

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The Effect of Diet on Gonadal Development of the Smooth Venus Clam Callista chione (Mollusca: Bivalvia) von Martínez-Pita, Inés, Sánchez-Lazo, Clara, Prieto, Emma, Moreno, Oscar

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Novel Syntaxin 11 Gene (STX11) Mutation in Three Argentinean Patients with Hemophagocytic Lymphohistiocytosis von Danielian, Silvia, Basile, Natalia, Rocco, Carlos, Prieto, Emma, Rossi, Jorge, Barsotti, Darío, Roche, Paul A, Bernasconi, Andrea, Oleastro, Matías, Zelazko, Marta, Braier, Jorge

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Síndrome de Bloch-Sulzberger: a propósito de un caso von Prieto Cuesta, Emma Divanna, Prieto Cuesta, Emilio Baddir, Prieto Cuesta, Clara Denisse, Brito Montalvo, Gianella Stefanía, León Ricaurte, Itzá Rayén, Reinoso Mendoza, Gabriel Alejandro

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The effect of diet on gonadal development of the smooth venus clam Callista chione von Martinez-Pita, Ines, Sanchez-Lazo, Clara, Prieto, Emma, Moreno, Oscar

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The effect of diet on gonadal development of the smooth venus clam Callista chione von Ma, Sanchez-Lazo, Clara, Prieto, Emma, Moreno, Oscar

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GLYCINE IN ACUTE MANAGEMENT OF ISOVALERICACIDÆMIA von Velazquez, Antonio, Prieto, EmmaC

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