Inflammatory Manifestations in Chronic Granulomatous Disease (CGD) von Rosenzweig, S. D.

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Common Severe Infections in Chronic Granulomatous Disease von Marciano, Beatriz E., Spalding, Christine, Fitzgerald, Alan, Mann, Daphne, Brown, Thomas, Osgood, Sharon, Yockey, Lynne, Darnell, Dirk N., Barnhart, Lisa, Daub, Janine, Boris, Lisa, Rump, Amy P., Anderson, Victoria L., Haney, Carissa, Kuhns, Douglas B., Rosenzweig, Sergio D., Kelly, Corin, Zelazny, Adrian, Mason, Tamika, See DeRavin, Suk, Kang, Elizabeth, Gallin, John I., Malech, Harry L., Olivier, Kenneth N., Uzel, Gulbu, Freeman, Alexandra F., Heller, Theo, Zerbe, Christa S., Holland, Steven M.

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Loss of B Cells in Patients with Heterozygous Mutations in IKAROS von Kuehn, Hye Sun, Boisson, Bertrand, Cunningham-Rundles, Charlotte, Reichenbach, Janine, Stray-Pedersen, Asbjørg, Gelfand, Erwin W, Maffucci, Patrick, Pierce, Keith R, Abbott, Jordan K, Voelkerding, Karl V, South, Sarah T, Augustine, Nancy H, Bush, Jeana S, Dolen, William K, Wray, Betty B, Itan, Yuval, Cobat, Aurelie, Sorte, Hanne Sørmo, Ganesan, Sundar, Prader, Seraina, Martins, Thomas B, Lawrence, Monica G, Orange, Jordan S, Calvo, Katherine R, Niemela, Julie E, Casanova, Jean-Laurent, Fleisher, Thomas A, Hill, Harry R, Kumánovics, Attila, Conley, Mary Ellen, Rosenzweig, Sergio D

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Mutations in PIK3CD Can Cause Hyper IgM Syndrome (HIGM) Associated with Increased Cancer Susceptibility von Crank, M. C., Grossman, J. K., Moir, S., Pittaluga, S., Buckner, C. M., Kardava, L., Agharahimi, A., Meuwissen, H., Stoddard, J., Niemela, J., Kuehn, H., Rosenzweig, S. D.

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Clinical and Histopathological Features and a Unique Spectrum of Organisms Significantly Associated with Chronic Granulomatous Disease Osteomyelitis during Childhood von Galluzzo, M. L., Hernandez, C., Davila, M. T. G., Pérez, L., Oleastro, M., Zelazko, M., Rosenzweig, S. D.

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Phagocyte immunodeficiencies and their infections von Rosenzweig, Sergio D, Holland, Steven M

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Activated STING in a Vascular and Pulmonary Syndrome von Liu, Yin, Jesus, Adriana A, Marrero, Bernadette, Yang, Dan, Ramsey, Suzanne E, Montealegre Sanchez, Gina A, Tenbrock, Klaus, Wittkowski, Helmut, Jones, Olcay Y, Kuehn, Hye Sun, Lee, Chyi-Chia R, DiMattia, Michael A, Cowen, Edward W, Gonzalez, Benito, Palmer, Ira, DiGiovanna, John J, Biancotto, Angelique, Kim, Hanna, Tsai, Wanxia L, Trier, Anna M, Huang, Yan, Stone, Deborah L, Hill, Suvimol, Kim, H. Jeffery, St. Hilaire, Cynthia, Gurprasad, Shakuntala, Plass, Nicole, Chapelle, Dawn, Horkayne-Szakaly, Iren, Foell, Dirk, Barysenka, Andrei, Candotti, Fabio, Holland, Steven M, Hughes, Jason D, Mehmet, Huseyin, Issekutz, Andrew C, Raffeld, Mark, McElwee, Joshua, Fontana, Joseph R, Minniti, Caterina P, Moir, Susan, Kastner, Daniel L, Gadina, Massimo, Steven, Alasdair C, Wingfield, Paul T, Brooks, Stephen R, Rosenzweig, Sergio D, Fleisher, Thomas A, Deng, Zuoming, Boehm, Manfred, Paller, Amy S, Goldbach-Mansky, Raphaela

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A 475 years-old founder effect involving IL12RB1: A highly prevalent mutation conferring Mendelian Susceptibility to Mycobacterial Diseases in European descendants von Yancoski, J., Rocco, C., Bernasconi, A., Oleastro, M., Bezrodnik, L., Vrátnica, C., Haerynck, F., Rosenzweig, S.D.

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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 von Zhou, Qing, Yang, Dan, Ombrello, Amanda K, Zavialov, Andrey V, Toro, Camilo, Zavialov, Anton V, Stone, Deborah L, Chae, Jae Jin, Rosenzweig, Sergio D, Bishop, Kevin, Barron, Karyl S, Kuehn, Hye Sun, Hoffmann, Patrycja, Negro, Alejandra, Tsai, Wanxia L, Cowen, Edward W, Pei, Wuhong, Milner, Joshua D, Silvin, Christopher, Heller, Theo, Chin, David T, Patronas, Nicholas J, Barber, John S, Lee, Chyi-Chia R, Wood, Geryl M, Ling, Alexander, Kelly, Susan J, Kleiner, David E, Mullikin, James C, Ganson, Nancy J, Kong, Heidi H, Hambleton, Sophie, Candotti, Fabio, Quezado, Martha M, Calvo, Katherine R, Alao, Hawwa, Barham, Beverly K, Jones, Anne, Meschia, James F, Worrall, Bradford B, Kasner, Scott E, Rich, Stephen S, Goldbach-Mansky, Raphaela, Abinun, Mario, Chalom, Elizabeth, Gotte, Alisa C, Punaro, Marilynn, Pascual, Virginia, Verbsky, James W, Torgerson, Troy R, Singer, Nora G, Gershon, Timothy R, Ozen, Seza, Karadag, Omer, Fleisher, Thomas A, Remmers, Elaine F, Burgess, Shawn M, Moir, Susan L, Gadina, Massimo, Sood, Raman, Hershfield, Michael S, Boehm, Manfred, Kastner, Daniel L, Aksentijevich, Ivona

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Penicillium piceum infection: diagnosis and successful treatment in chronic granulomatous disease von Santos, P. E., Piontelli, E., Shea, Y. R., Galluzzo, M. L., Holland, S. M., Zelazko, M. E., Rosenzweig, S. D.

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Morphologic and electronic changes induced by thermally supported hydrogen cleaning of GaAs(110) facets von Rosenzweig, D. S., Schnedler, M., Dunin-Borkowski, R. E., Ebert, Ph, Eisele, H.

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Interferon-γ receptor 1 promoter polymorphisms: population distribution and functional implications von Rosenzweig, Sergio D, Schäffer, Alejandro A, Ding, Li, Sullivan, Rachel, Enyedi, Balasz, Yim, Jae-Joon, Cook, James L, Musser, James M, Holland, Steven M

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Atomically resolved study of initial stages of hydrogen etching and adsorption on GaAs(110) von Rosenzweig, D. S., Hansemann, M. N. L., Schnedler, M., Ebert, Ph, Eisele, H.

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Variable Presentation of Disseminated Nontuberculous Mycobacterial Infections in a Family with an Interferon-γ Receptor Mutation von Han, Jin-Young, Rosenzweig, Sergio D., Church, Joseph A., Holland, Steven M., Ross, Lawrence A.

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Primary Immunodeficiency Diseases and Bacillus Calmette-Guérin (BCG)-Vaccine–Derived Complications: A Systematic Review von Fekrvand, Saba, Yazdani, Reza, Olbrich, Peter, Gennery, Andrew, Rosenzweig, Sergio D., Condino-Neto, Antonio, Azizi, Gholamreza, Rafiemanesh, Hosein, Hassanpour, Gholamreza, Rezaei, Nima, Abolhassani, Hassan, Aghamohammadi, Asghar

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Nodular regenerative hyperplasia in X-linked agammaglobulinemia: An underestimated and severe complication von Nunes-Santos, Cristiane J., Koh, Christopher, Rai, Anjali, Sacco, Keith, Marciano, Beatriz E., Kleiner, David E., Marko, Jamie, Bergerson, Jenna R.E., Stack, Michael, Rivera, Maria M., Constantine, Gregory, Strober, Warren, Uzel, Gulbu, Fuss, Ivan J., Notarangelo, Luigi D., Holland, Steven M., Rosenzweig, Sergio D., Heller, Theo

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Defects in the interferon-γ and interleukin-12 pathways von Rosenzweig, Sergio D., Holland, Steven M.

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Clinical features of dominant and recessive interferon γ receptor 1 deficiencies von Dorman, Susan E, Picard, Capucine, Lammas, David, Heyne, Klaus, van Dissel, Jaap T, Baretto, Richard, Rosenzweig, Sergio D, Newport, Melanie, Levin, Michael, Roesler, Joachim, Kumararatne, Dinakantha, Casanova, Jean-Laurent, Holland, Steven M

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Gastrointestinal Involvement in Chronic Granulomatous Disease von Marciano, Beatriz E, Rosenzweig, Sergio D, Kleiner, David E, Anderson, Victoria L, Darnell, Dirk N, Anaya-O'Brien, Sandra, Hilligoss, Dianne M, Malech, Harry L, Gallin, John I, Holland, Steven M

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Genomic characterization of lymphomas in patients with inborn errors of immunity von Ye, Xiaofei, Maglione, Paul J., Wehr, Claudia, Li, Xiaobo, Wang, Yating, Abolhassani, Hassan, Deripapa, Elena, Liu, Dongbing, Borte, Stephan, Du, Likun, Wan, Hui, Plötner, Andreas, Giannoula, Yvonne, Ko, Huai-Bin, Hou, Yong, Zhu, Shida, Grossman, Jennifer K., Sander, Birgitta, Grimbacher, Bodo, Hammarström, Lennart, Fedorova, Alina, Rosenzweig, Sergio D., Shcherbina, Anna, Wu, Kui, Warnatz, Klaus, Cunningham-Rundles, Charlotte, Pan-Hammarström, Qiang

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