Increased STAT1 Amounts Correlate with the Phospho-STAT1 Level in STAT1 Gain-of-function Defects von Bernasconi, Andrea R., Yancoski, Judith, Villa, Mariana, Oleastro, Matías M., Galicchio, Miguel, Rossi, Jorge G.

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X-linked agammaglobulinemia in adults. Clinical evolution von Giorgetti, Orlando B, Paolini, María V, Oleastro, Matías M, Fernández Romero, Diego S

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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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Noninfectious complications in patients with pediatric-onset common variable immunodeficiency correlated with defects in somatic hypermutation but not in class-switch recombination von Almejún, María Belén, PhD, Campos, Bárbara Carolina, Patiño, Virginia, MD, Galicchio, Miguel, MD, Zelazko, Marta, MD, Oleastro, Matías, MD, Oppezzo, Pablo, PhD, Danielian, Silvia, PhD

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Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases von Conti, Francesca, MD, PhD, Lugo-Reyes, Saul Oswaldo, MD, Blancas Galicia, Lizbeth, MD, He, Jianxin, MD, Aksu, Güzide, MD, Borges de Oliveira, Edgar, PhD, Deswarte, Caroline, MSc, Hubeau, Marjorie, PhD, Karaca, Neslihan, MD, de Suremain, Maylis, AS, Guérin, Antoine, MSc, Baba, Laila Ait, PhD, Prando, Carolina, MD, PhD, Guerrero, Gloria G., PhD, Emiroglu, Melike, MD, Öz, Fatma Nur, MD, Yamazaki Nakashimada, Marco Antonio, MD, Gonzalez Serrano, Edith, MD, Espinosa, Sara, MD, PhD, Barlan, Isil, MD, Pérez, Nestor, MD, PhD, Regairaz, Lorena, MD, Guidos Morales, Héctor Eduardo, MD, Bezrodnik, Liliana, MD, Di Giovanni, Daniela, MD, Dbaibo, Ghassan, MD, Ailal, Fatima, MD, Galicchio, Miguel, MD, Oleastro, Matias, MD, Chemli, Jalel, MD, Danielian, Silvia, PhD, Perez, Laura, BSc, Ortega, Maria Claudia, MD, Soto Lavin, Susana, MD, PhD, Hertecant, Joseph, MD, Anal, Ozden, MD, Kechout, Nadia, MD, Al-Idrissi, Eman, MD, ElGhazali, Gehad, MD, PhD, Bondarenko, Anastasia, MD, Chernyshova, Liudmyla, MD, Ciznar, Peter, MD, Herbigneaux, Rose-Marie, MD, Diabate, Aminata, AS, Ndaga, Stéphanie, AS, Konte, Barik, AS, Czarna, Ambre, AS, Migaud, Mélanie, AS, Pedraza-Sánchez, Sigifredo, PhD, Zaidi, Mussaret Bano, MD, Msc, Vogt, Guillaume, PhD, Blanche, Stéphane, MD, Benmustapha, Imen, MD, Mansouri, Davood, MD, Abel, Laurent, MD, PhD, Boisson-Dupuis, Stéphanie, PhD, Mahlaoui, Nizar, MD, MSc, MPH, Bousfiha, Ahmed Aziz, MD, Picard, Capucine, MD, PhD, Barbouche, Ridha, MD, PhD, Al-Muhsen, Saleh, MD, Espinosa-Rosales, Francisco J., MD, Kütükçüler, Necil, MD, Condino-Neto, Antonio, MD, PhD, Casanova, Jean-Laurent, MD, PhD, Bustamante, Jacinta, MD, PhD

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Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants von Kagawa, Reiko, MD, Fujiki, Ryoji, MS, Tsumura, Miyuki, PhD, Sakata, Sonoko, MD, Nishimura, Shiho, MD, Itan, Yuval, PhD, Kong, Xiao-Fei, MD, PhD, Kato, Zenichiro, MD, PhD, Ohnishi, Hidenori, MD, PhD, Hirata, Osamu, MD, PhD, Saito, Satoshi, MD, Ikeda, Maiko, MD, El Baghdadi, Jamila, PhD, Bousfiha, Aziz, MD, Fujiwara, Kaori, MD, Oleastro, Matias, MD, Yancoski, Judith, PhD, Perez, Laura, BSc, Danielian, Silvia, PhD, Ailal, Fatima, MD, Takada, Hidetoshi, MD, PhD, Hara, Toshiro, MD, PhD, Puel, Anne, PhD, Boisson-Dupuis, Stéphanie, PhD, Bustamante, Jacinta, MD, PhD, Casanova, Jean-Laurent, MD, PhD, Ohara, Osamu, PhD, Okada, Satoshi, MD, PhD, Kobayashi, Masao, MD, PhD

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Síndrome de activación macrofágica en pacientes con artritis idiopática juvenil sistémica: análisis de 17 casos observados en un hospital terciario von Russo, Ricardo A. G, Katsicas, María M, Oleastro, Matías M, Zelazko, Marta

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A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency von Hacein-Bey-Abina, Salima, Pai, Sung-Yun, Gaspar, H. Bobby, Armant, Myriam, Berry, Charles C, Blanche, Stephane, Bleesing, Jack, Blondeau, Johanna, de Boer, Helen, Buckland, Karen F, Caccavelli, Laure, Cros, Guilhem, De Oliveira, Satiro, Fernández, Karen S, Guo, Dongjing, Harris, Chad E, Hopkins, Gregory, Lehmann, Leslie E, Lim, Annick, London, Wendy B, van der Loo, Johannes C.M, Malani, Nirav, Male, Frances, Malik, Punam, Marinovic, M. Angélica, McNicol, Anne-Marie, Moshous, Despina, Neven, Benedicte, Oleastro, Matías, Picard, Capucine, Ritz, Jerome, Rivat, Christine, Schambach, Axel, Shaw, Kit L, Sherman, Eric A, Silberstein, Leslie E, Six, Emmanuelle, Touzot, Fabien, Tsytsykova, Alla, Xu-Bayford, Jinhua, Baum, Christopher, Bushman, Frederic D, Fischer, Alain, Kohn, Donald B, Filipovich, Alexandra H, Notarangelo, Luigi D, Cavazzana, Marina, Williams, David A, Thrasher, Adrian J

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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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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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Inherited p40phox deficiency differs from classic chronic granulomatous disease von van de Geer, Annemarie, Nieto-Patlán, Alejandro, Kuhns, Douglas B, Tool, Anton Tj, Arias, Andrés A, Bouaziz, Matthieu, de Boer, Martin, Franco, José Luis, Gazendam, Roel P, van Hamme, John L, van Houdt, Michel, van Leeuwen, Karin, Verkuijlen, Paul Jh, van den Berg, Timo K, Alzate, Juan F, Arango-Franco, Carlos A, Batura, Vritika, Bernasconi, Andrea R, Boardman, Barbara, Booth, Claire, Burns, Siobhan O, Cabarcas, Felipe, Bensussan, Nadine Cerf, Charbit-Henrion, Fabienne, Corveleyn, Anniek, Deswarte, Caroline, Azcoiti, María Esnaola, Foell, Dirk, Gallin, John I, Garcés, Carlos, Guedes, Margarida, Hinze, Claas H, Holland, Steven M, Hughes, Stephen M, Ibañez, Patricio, Malech, Harry L, Meyts, Isabelle, Moncada-Velez, Marcela, Moriya, Kunihiko, Neves, Esmeralda, Oleastro, Matias, Perez, Laura, Rattina, Vimel, Oleaga-Quintas, Carmen, Warner, Neil, Muise, Aleixo M, López, Jeanet Serafín, Trindade, Eunice, Vasconcelos, Julia, Vermeire, Séverine, Wittkowski, Helmut, Worth, Austen, Abel, Laurent, Dinauer, Mary C, Arkwright, Peter D, Roos, Dirk, Casanova, Jean-Laurent, Kuijpers, Taco W, Bustamante, Jacinta

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Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome von Leiding, Jennifer W., Vogel, Tiphanie P., Smith, Madison R., Carisey, Alexandre, Vargas-Hernández, Alexander, Silva-Carmona, Manuel, Neven, Bénédicte, Ronan Leahy, Timothy, Taskinen, Mervi, Kostyuchenko, Larysa, Scherbina, Anna, Bauer, Cindy S., Giovannini-Chami, Lisa, Romberg, Neil, Prince, Benjamin T., Bohnsack, John, Pachlopnik Schmid, Jana, Bahna, Sami, Brothers, Shannon, Chan, Alice Y., Chandrakasan, Shanmuganathan, Christiansen, Mette, Cole, Theresa, Desai, Mukesh M., Gottrand, Frédéric, Grimbacher, Bodo, Hoffman, Hal M., Guerrerio, Anthony L., Kainulainen, Leena, Lawrence, Monica G., Martelius, Timi, Neth, Olaf, Lugo Reyes, Saúl Oswaldo, Russell, Mark A., Schejter, Yael, Skevofilax, Effie, Suan, Daniel, Velasco, Helena, Walkovich, Kelly, Aleshkevich, Svetlana, Allende, Luis M., Atschekzei, Faranaz, Aygunes, Utku, Barlogis, Vincent, Belko, John, Bezrodnik, Liliana, Biebl, Ariane, Caldirola, Maria Soledad, Castelle, Martin, Cokugras, Haluk, Cox, Fionnuala, Dalgic, Buket, ASH Dalm, Virgil, Dujovny, Tal, Eken, Ahmet, Fabre, Alexandre, Fischer, Alain, Hannibal, Mark, Huppert, Laura, Karakoc-Aydiner, Elif, Pac Kisaarslan, Ayşenur, Kiykim, Ayca, Klocperk, Adam, Kuzmenko, Natalia, Lianou, Dimitra, Lorenz, Myriam Ricarda, Manson, Ania, Marega, Lia Furlaneto, Nolan, David, Norlin, Anna-Carin, Oleastro, Matias, Ozcan, Alper, Picard, Capucine, Polychronopoulou, Sophia, Quesada, Juan Francisco, Randall, Katrina L., Resin, Geraldine, Rodina, Yulia, Rohrlich, Pierre, Sachs, Johnathan, Sakovich, Inga, Santarlas, Christopher, Scheffler Mendoza, Selma C., Schwarz, Klaus, Sediva, Anna, Slatter, Mary, Sleasman, John, Suratannon, Narissara, Tanita, Kay, Travis, Stephen, Tsinti, Maria, Unal, Ekrem, Urdinez, Luciano, Vazquez-Gomez, Felisa, Weiss, Mitchell J., Zhang, Yu, Seppänen, Mikko R.J., Sogkas, Georgios, Milner, Joshua D., Forbes Satter, Lisa R.

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Revisiting Human IL-12Rβ1 Deficiency: A Survey of 141 Patients From 30 Countries von de Beaucoudrey, Ludovic, Samarina, Arina, Bustamante, Jacinta, Cobat, Aurélie, Boisson-Dupuis, Stéphanie, Feinberg, Jacqueline, Al-Muhsen, Saleh, Jannière, Lucile, Rose, Yoann, de Suremain, Maylis, Filipe-Santos, Orchidée, Chapgier, Ariane, Picard, Capucine, Dogu, Figen, Ikinciogullari, Aydan, Tanir, Gonul, Al-Hajjar, Sami, Frayha, Husn H., AlSum, Zobaida, Al-Ajaji, Sulaiman, Alangari, Abdullah, Al-Ghonaium, Abdulaziz, Adimi, Parisa, Mansouri, Davood, Ben-Mustapha, Imen, Yancoski, Judith, Garty, Ben-Zion, Rodriguez-Gallego, Carlos, Caragol, Isabel, Kumararatne, Dinakantha S., Patel, Smita, Doffinger, Rainer, Jeppsson, Olle, Reichenbach, Janine, Nadal, David, Boyko, Yaryna, Pietrucha, Barbara, Anderson, Suzanne, Levin, Michael, Schandené, Liliane, Schepers, Kinda, Efira, André, Mascart, Françoise, Matsuoka, Masao, Siegrist, Claire-Anne, Frecerova, Klara, Blüetters-Sawatzki, Renate, Freihorst, Joachim, Baumann, Ulrich, Richter, Darko, Haerynck, Filomeen, Novelli, Vas, Lammas, David, Vermylen, Christiane, Tuerlinckx, David, Fleckenstein, Bernhard, Levy, Jacob, Raj, Revathi, Cohen, Aileen Cleary, Lewis, David B., Yang, Kuender D., Jiang, Liping, Yang, Xiqiang, Xie, Yuanyuan, Lee, Pamela Pui Wah, Chan, Koon Wing, Chen, Tong-Xin, Castro, Gabriela, Natera, Ivelisse, Codoceo, Ana, King, Alejandra, Bezrodnik, Liliana, Gaillard, Maria Isabel, Grumach, Anete Sevciovic, da Silva Duarte, Alberto Jose, Aldana, Ruth, Espinosa-Rosales, Francisco Javier, Bousfiha, Ahmed Aziz, Baghdadi, Jamila El, Aksu, Guzide, Keser, Melike, Somer, Ayper, Hatipoglu, Nevin, Aydogmus, Çigdem, Asilsoy, Suna, Camcioglu, Yildiz, Gülle, Saniye, Ozgur, Tuba T., Ozen, Meteran, Oleastro, Matias, Bernasconi, Andrea, Mamishi, Setareh, Parvaneh, Nima, Rosenzweig, Sergio, Barbouche, Ridha, Pedraza, Sigifredo, Lau, Yu Lung, Ehlayel, Mohammad S., Fieschi, Claire, Casanova, Jean-Laurent

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Long-Term Outcome of Gene Therapy for X-Linked Severe Combined Immunodeficiency (SCID-X1) Using an Enhancer-Deleted Self-Inactivating Gammaretroviral Vector von Pai, Sung-Yun, Nagarsheth, Nisha, Prockop, Susan, Armant, Myriam, Kohn, Donald B., Marsh, Rebecca A., Booth, Claire, Everett, John K., Bleesing, Jack, Chellapandian, Deepak, Dansereau, Colleen, de Oliveira, Satiro, London, Wendy B., Marinovic, M. Angélica, Moore, Theodore B., Oleastro, Matias, O'Toole, Grainne, Vander Lugt, Mark, Urdinez, Luciano, Walkovich, Kelly J., Walter, Jolan E., Schambach, Axel, Thrasher, Adrian J., Bushman, Frederic D., Williams, David A

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COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report von McDonnell, John, Lane, Adam, Abolhassani, Hassan, Abraham, Roshini S., Al-Faris, Eman Hesham, Alfaro-Murillo, Alberto, AlKhater, Suzan A., Alsaati, Nouf, Doss, Alexa Michelle Altman, Anderson, Melissa, Angarola, Ernestina, Ariue, Barbara, Assa’ad, Amal H., Aytekin, Caner, Bank, Meaghan, Bleesing, Jack, Boesing, John, Cabanillas, Diana, Callahan, Meghan A., Carrabba, Maria, Catanzaro, Jason R., Chan, Samantha, Chandra, Sharat, Chapdelaine, Hugo, Chavoshzadeh, Zahra, Chong, Hey Jin, Connors, Lori, Consonni, Filippo, Correa-Jimenez, Oscar, D’Astous-Gauthier, Katherine, Deshpande, Deepti R., Diaz-Cabrera, Natalie M., El-Owaidy, Rasha, ElGhazali, Gehad, Al-Hammadi, Suleiman, Fabio, Giovanna, Feng, Jin, Fernandez, James M., Fill, Lauren, Frenck, Robert W., Giardino, Giuliana, Galant-Swafford, Jessica, Gambineri, Eleonora, Garabedian, Elizabeth K., Grecco, Octavio, Pan-Hammarström, Qiang, Hammarström, Lennart, Heimall, Jennifer, Hernandez-Molina, Gabriela, Hostoffer, Robert W., Hristova, Nataliya, Hsiao, Kuang-Chih, Jalil, Maaz, Jean, Tiffany, Jeong, Stephanie, Jhaveri, Devi, Joshi, Avni Y., Kanarek, Henry J., Khoury, Ruby, Kumar, Ashish, Lecerf, Kelsey, Leiding, Jennifer W., Lesmana, Harry, Lim, Xin Rong, Lopes, Joao Pedro, Tarquini, Lucia, Lundgren, Ingrid S., Magnusson, Julieann, Marinho, Ana Karolina B. B., Martone, Giulia M., Mechtler, Annamaria G., Mustillo, Peter J., Naderi, Asal Gharib, Nell, Jeremy, Notarangelo, Luigi, Oleastro, Matias, Patel, Neil R., Petrovic, Gordana, Prince, Benjamin T., Rabusin, Marco, Raje, Nikita, Salemi, Negin, Scalchunes, Christopher, Schuval, Susan J., Seneviratne, Suranjith L., Shin, Junghee Jenny, Siddiqi, Abeer, Signa, Sara, Sobh, Ali, Lima, Fabiana Mascarenhas Souza, Stenehjem, Kristen K., Tang, Monica, Barros, Myrthes Toledo, Verbsky, James, Voelker, Dayne H., Volpi, Stefano, Wu, Eveline Y., Zhou, Jessie J., Sullivan, Kathleen E., Marsh, Rebecca

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Combined liver and hematopoietic stem cell transplantation in patients with X-linked hyper-IgM syndrome von Bucciol, Giorgia, Nicholas, Sarah K., Calvo, Pier Luigi, Cant, Andrew, Edgar, J. David M., Español, Teresa, Ferrua, Francesca, Galicchio, Miguel, Gennery, Andrew R., Hadzic, Nedim, Hanson, I. Celine, Kusminsky, Gustavo, Lange, Andrzej, Lanternier, Fanny, Mahlaoui, Nizar, Moshous, Despina, Nademi, Zohreh, Neven, Benedicte, Oleastro, Matias, Porta, Fulvio, Quarello, Paola, Silva, Marcelo, Slatter, Mary A., Soncini, Elena, Stefanowicz, Marek, Tandoi, Francesco, Teisseyre, Mikołaj, Torgerson, Troy R., Veys, Paul, Weinacht, Katja G., Wolska-Kuśnierz, Beata, Pirenne, Jacques, de la Morena, M. Teresa, Meyts, Isabelle

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Combined liver and hematopoietic stem cell transplantation in patients with X-linked hyper-IgM syndrome von Bucciol, Giorgia, Nicholas, Sarah K, Calvo, Pier Luigi, Cant, Andrew, Edgar, J. David M, Espanol, Teresa, Ferrua, Francesca, Galicchio, Miguel, Gennery, Andrew R, Hadzic, Nedim, Hanson, I. Celine, Kusminsky, Gustavo, Lange, Andrzej, Lanternier, Fanny, Mahlaoui, Nizar, Moshous, Despina, Nademi, Zohreh, Neven, Benedicte, Oleastro, Matias, Porta, Fulvio, Quarello, Paola, Silva, Marcelo, Slatter, Mary A, Soncini, Elena, Stefanowicz, Marek, Tandoi, Francesco, Teisseyre, Mikolaj, Torgerson, Troy R, Veys, Paul, Weinacht, Katja G, Wolska-Kusnierz, Beata, Pirenne, Jacques, de la Morena, M. Teresa, Meyts, Isabelle

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Inherited p40^sup phox^ deficiency differs from classic chronic granulomatous disease von van de Geer, Annemarie, van Hamme, John L, van Houdt, Michel, van Leeuwen, Karin, Verkuijlen, Paul J H, van den Berg, Timo K, Alzate, Juan F, Arango-Franco, Carlos A, Batura, Vritika, Bernasconi, Andrea R, Boardman, Barbara, Nieto-Patlán, Alejandro, Booth, Claire, Burns, Siobhan O, Cabarcas, Felipe, Bensussan, Nadine Cerf, Charbit-Henrion, Fabienne, Corveleyn, Anniek, Deswarte, Caroline, Azcoiti, María Esnaola, Foell, Dirk, Gallin, John I, Kuhns, Douglas B, Garcés, Carlos, Guedes, Margarida, Hinze, Claas H, Holland, Steven M, Hughes, Stephen M, Ibañez, Patricio, Malech, Harry L, Meyts, Isabelle, Moncada-Velez, Marcela, Moriya, Kunihiko, Tool, Anton T J, Neves, Esmeralda, Oleastro, Matias, Perez, Laura, Rattina, Vimel, Oleaga-Quintas, Carmen, Warner, Neil, Muise, Aleixo M, López, Jeanet Serafín, Trindade, Eunice, Vasconcelos, Julia, Arias, Andrés A, Vermeire, Séverine, Wittkowski, Helmut, Worth, Austen, Abel, Laurent, Dinauer, Mary C, Arkwright, Peter D, Roos, Dirk, Casanova, Jean-Laurent, Kuijpers, Taco W, Bustamante, Jacinta, Bouaziz, Matthieu, de Boer, Martin, Franco, José Luis, Gazendam, Roel P

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Inherited p40phox deficiency differs from classic chronic granulomatous disease von van de Geer, Annemarie, Nieto-Patlan, Alejandro, Kuhns, Douglas B, Tool, Anton T.J, Arias, Andres A, Bouaziz, Matthieu, de Boer, Martin, Luis Franco, Jose, Gazendam, Roel P, van Hamme, John L, van Houdt, Michel, van Leeuwen, Karin, Verkuijlen, Paul J.H, van den Berg, Timo K, Alzate, Juan F, Arango-Franco, Carlos A, Batura, Vritika, Bernasconi, Andrea R, Boardman, Barbara, Booth, Claire, Burns, Siobhan O, Cabarcas, Felipe, Bensussan, Nadine Cerf, Charbit-Henrion, Fabienne, Corveleyn, Anniek, Deswarte, Caroline, Esnaola Azcoiti, Maria, Foell, Dirk, Gallin, John I, Garces, Carlos, Guedes, Margarida, Hinze, Claas H, Holland, Steven M, Hughes, Stephen M, Ibanez, Patricio, Malech, Harry L, Meyts, Isabelle, Moncada-Velez, Marcela, Moriya, Kunihiko, Neves, Esmeralda, Oleastro, Matias, Perez, Laura, Rattina, Vimel, Oleaga-Quintas, Carmen, Warner, Neil, Muise, Aleixo M, Serafin Lopez, Jeanet, Trindade, Eunice, Vasconcelos, Julia, Vermeire, Severine, Wittkowski, Helmut, Worth, Austen, Abel, Laurent, Dinauer, Mary C, Arkwright, Peter D, Roos, Dirk, Casanova, Jean-Laurent, Kuijpers, Taco W, Bustamante, Jacinta

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X-linked chronic granulomatous disease: first report of mutations in patients of Argentina von Barese, Cecilia, Copelli, Silvia, Zandomeni, Rubén, Oleastro, Matías, Zelazko, Marta, Rivas, Eva María

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