Lentiviral gene therapy for X-linked chronic granulomatous disease von Kohn, Donald B., Booth, Claire, Kang, Elizabeth M., Pai, Sung-Yun, Shaw, Kit L., Santilli, Giorgia, Armant, Myriam, Buckland, Karen F., Choi, Uimook, De Ravin, Suk See, Dorsey, Morna J., Kuo, Caroline Y., Leon-Rico, Diego, Rivat, Christine, Izotova, Natalia, Gilmour, Kimberly, Snell, Katie, Dip, Jinhua Xu-Bayford, Darwish, Jinan, Morris, Emma C., Terrazas, Dayna, Wang, Leo D., Bauser, Christopher A., Paprotka, Tobias, Kuhns, Douglas B., Gregg, John, Raymond, Hayley E., Everett, John K., Honnet, Geraldine, Biasco, Luca, Newburger, Peter E., Bushman, Frederic D., Grez, Manuel, Gaspar, H. Bobby, Williams, David A., Malech, Harry L., Galy, Anne, Thrasher, Adrian J.

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Peritoneal tissue-resident macrophages are metabolically poised to engage microbes using tissue-niche fuels von Davies, Luke C., Rice, Christopher M., Palmieri, Erika M., Taylor, Philip R., Kuhns, Douglas B., McVicar, Daniel W.

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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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X-linked Carriers of Chronic Granulomatous Disease: Illness, Lyonization and Stability von Marciano, Beatriz E., MD, Zerbe, Christa S., MD, Falcone, E. Liana, MD PhD, Ding, Li, MD, DeRavin, Suk See, MD PhD, Daub, Janine, CRNP, Kreuzburg, Samantha, CRNP, Yockey, Lynne, CRNP, Hunsberger, Sally, PHD, Foruraghi, Ladan, CRNP, Barnhart, Lisa A., CRNP, Matharu, Kabir, MD, Anderson, Victoria, CRNP, Darnell, Dirk N., CRNP, Frein, Cathleen, CRNP, Fink, Danielle L., MS, Lau, Karen P., MS, Long Priel, Debra A., MS, Gallin, John I., MD, Malech, Harry L., MD, Uzel, Gulbu, MD, Freeman, Alexandra F., MD, Kuhns, Douglas B., PhD, Rosenzweig, Sergio D., MD PhD, Holland, Steven M., MD

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A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency von Zhou, Qing, Lee, Geun-Shik, Brady, Jillian, Datta, Shrimati, Katan, Matilda, Sheikh, Afzal, Martins, Marta S, Bunney, Tom D, Santich, Brian H, Moir, Susan, Kuhns, Douglas B, Long Priel, Debra A, Ombrello, Amanda, Stone, Deborah, Ombrello, Michael J, Khan, Javed, Milner, Joshua D, Kastner, Daniel L, Aksentijevich, Ivona

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A phase III randomized crossover trial of plerixafor versus G-CSF for treatment of WHIM syndrome von McDermott, David H, Velez, Daniel, Cho, Elena, Cowen, Edward W, DiGiovanna, John J, Pastrana, Diana V, Buck, Christopher B, Calvo, Katherine R, Gardner, Pamela J, Rosenzweig, Sergio D, Stratton, Pamela, Merideth, Melissa A, Kim, H Jeffrey, Brewer, Carmen, Katz, James D, Kuhns, Douglas B, Malech, Harry L, Follmann, Dean, Fay, Michael P, Murphy, Philip M

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Isolation and Functional Analysis of Human Neutrophils von Kuhns, Douglas B., Priel, Debra A. Long, Chu, Jessica, Zarember, Kol A.

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Chromothriptic Cure of WHIM Syndrome von McDermott, David H., Gao, Ji-Liang, Liu, Qian, Siwicki, Marie, Martens, Craig, Jacobs, Paejonette, Velez, Daniel, Yim, Erin, Bryke, Christine R., Hsu, Nancy, Dai, Zunyan, Marquesen, Martha M., Stregevsky, Elina, Kwatemaa, Nana, Theobald, Narda, Long Priel, Debra A., Pittaluga, Stefania, Raffeld, Mark A., Calvo, Katherine R., Maric, Irina, Desmond, Ronan, Holmes, Kevin L., Kuhns, Douglas B., Balabanian, Karl, Bachelerie, Françoise, Porcella, Stephen F., Malech, Harry L., Murphy, Philip M.

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Human PI3Kγ deficiency and its microbiota-dependent mouse model reveal immunodeficiency and tissue immunopathology von Takeda, Andrew J., Maher, Timothy J., Zhang, Yu, Lanahan, Stephen M., Bucklin, Molly L., Compton, Susan R., Tyler, Paul M., Comrie, William A., Matsuda, Makoto, Olivier, Kenneth N., Pittaluga, Stefania, McElwee, Joshua J., Long Priel, Debra A., Kuhns, Douglas B., Williams, Roger L., Mustillo, Peter J., Wymann, Matthias P., Koneti Rao, V., Lucas, Carrie L.

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Signal transducer and activator of transcription 1 ( STAT1 ) gain-of-function mutations and disseminated coccidioidomycosis and histoplasmosis von Sampaio, Elizabeth P., MD, PhD, Hsu, Amy P., BA, Pechacek, Joseph, BA, Bax, Hannelore I., MD, Dias, Dalton L., BA, Paulson, Michelle L., MD, Chandrasekaran, Prabha, PhD, Rosen, Lindsey B., BS, Carvalho, Daniel S., PhD, Ding, Li, MD, Vinh, Donald C., MD, Browne, Sarah K., MD, Datta, Shrimati, PhD, Milner, Joshua D., MD, Kuhns, Douglas B., PhD, Long Priel, Debra A., BS, Sadat, Mohammed A., MD, Shiloh, Michael, MD, PhD, De Marco, Brendan, MD, Alvares, Michael, MD, Gillman, Jason W., MD, Ramarathnam, Vivek, MD, de la Morena, Maite, MD, Bezrodnik, Liliana, MD, Moreira, Ileana, MD, Uzel, Gulbu, MD, Johnson, Daniel, MD, Spalding, Christine, RN, Zerbe, Christa S., MD, Wiley, Henry, MD, Greenberg, David E., MD, Hoover, Susan E., MD, PhD, Rosenzweig, Sergio D., MD, PhD, Galgiani, John N., MD, Holland, Steven M., MD

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Allogeneic Reduced-Intensity Hematopoietic Stem Cell Transplantation for Chronic Granulomatous Disease: a Single-Center Prospective Trial von Parta, Mark, Kelly, Corin, Kwatemaa, Nana, Theobald, Narda, Hilligoss, Diane, Qin, Jing, Kuhns, Douglas B., Zerbe, Christa, Holland, Steven M., Malech, Harry, Kang, Elizabeth M.

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Hematologically important mutations: Leukocyte adhesion deficiency (second update) von Roos, Dirk, van Leeuwen, Karin, Madkaikar, Manisha, Kambli, Priyanka M., Gupta, Maya, Mathews, Vikram, Rawat, Amit, Kuhns, Douglas B., Holland, Steven M., de Boer, Martin, Kanegane, Hirokazu, Parvaneh, Nima, Lorenz, Myriam, Schwarz, Klaus, Klein, Christoph, Sherkat, Roya, Jafari, Mahbube, Wolach, Baruch, den Dunnen, Johan T., Kuijpers, Taco W., Köker, M. Yavuz

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TNF overproduction impairs epithelial staphylococcal response in hyper IgE syndrome von Myles, Ian A, Anderson, Erik D, Earland, Noah J, Zarember, Kol A, Sastalla, Inka, Williams, Kelli W, Gough, Portia, Moore, Ian N, Ganesan, Sundar, Fowler, Cedar J, Laurence, Arian, Garofalo, Mary, Kuhns, Douglas B, Kieh, Mark D, Saleem, Arhum, Welch, Pamela A, Darnell, Dirk A, Gallin, John I, Freeman, Alexandra F, Holland, Steven M, Datta, Sandip K

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Abnormal Nasal Nitric Oxide Production, Ciliary Beat Frequency, and Toll-like Receptor Response in Pulmonary Nontuberculous Mycobacterial Disease Epithelium von FOWLER, Cedar J, OLIVIER, Kenneth N, DAUB, Janine, HANEY, Carissa, SHELHAMER, James H, BRYANT, Clare E, HOLLAND, Steven M, LEUNG, Janice M, SMITH, Caroline C, HUTH, Andrea G, ROOT, Heather, KUHNS, Douglas B, LOGUN, Carolea, ZELAZNY, Adrian, FREIN, Cathleen A

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The Changing Paradigm of Management of Liver Abscesses in Chronic Granulomatous Disease von Straughan, David M, McLoughlin, Kaitlin C, Mullinax, John E, Marciano, Beatriz E, Freeman, Alexandra F, Anderson, Victoria L, Uzel, Gulbu, Azoury, Said C, Sorber, Rebecca, Quadri, Humair S, Malech, Harry L, DeRavin, Suk See, Kamal, Natasha, Koh, Christopher, Zerbe, Christa S, Kuhns, Douglas B, Gallin, John I, Heller, Theo, Holland, Steven M, Rudloff, Udo

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Hematologically important mutations: X-linked chronic granulomatous disease (third update) von Roos, Dirk, Kuhns, Douglas B., Maddalena, Anne, Roesler, Joachim, Lopez, Juan Alvaro, Ariga, Tadashi, Avcin, Tadej, de Boer, Martin, Bustamante, Jacinta, Condino-Neto, Antonio, Di Matteo, Gigliola, He, Jianxin, Hill, Harry R., Holland, Steven M., Kannengiesser, Caroline, Köker, M. Yavuz, Kondratenko, Irina, van Leeuwen, Karin, Malech, Harry L., Marodi, László, Nunoi, Hiroyuki, Stasia, Marie-José, Ventura, Anna Maria, Witwer, Carl T., Wolach, Baruch, Gallin, John I.

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IKBKG (NEMO) 5′ Untranslated Splice Mutations Lead to Severe, Chronic Disseminated Mycobacterial Infections von Hsu, Amy P, Zerbe, Christa S, Foruraghi, Ladan, Iovine, Nicole M, Leiding, Jennifer W, Mushatt, David M, Wild, Laurianne, Kuhns, Douglas B, Holland, Steven M

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Hypomorphic Rag mutations can cause destructive midline granulomatous disease von De Ravin, Suk See, Cowen, Edward W., Zarember, Kol A., Whiting-Theobald, Narda L., Kuhns, Douglas B., Sandler, Netanya G., Douek, Daniel C., Pittaluga, Stefania, Poliani, Pietro L., Lee, Yu Nee, Notarangelo, Luigi D., Wang, Lei, Alt, Frederick W., Kang, Elizabeth M., Milner, Joshua D., Niemela, Julie E., Fontana-Penn, Mary, Sinal, Sara H., Malech, Harry L.

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Hematologically important mutations: The autosomal recessive forms of chronic granulomatous disease (second update) von Roos, Dirk, Kuhns, Douglas B., Maddalena, Anne, Bustamante, Jacinta, Kannengiesser, Caroline, de Boer, Martin, van Leeuwen, Karin, Köker, M. Yavuz, Wolach, Baruch, Roesler, Joachim, Malech, Harry L., Holland, Steven M., Gallin, John I., Stasia, Marie-José

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Complete Myeloperoxidase Deficiency: Beware the “False-Positive” Dihydrorhodamine Oxidation von Milligan, Ki Lee, MD, Mann, Daphne, BSN, Rump, Amy, MSN, CRNP, Anderson, Victoria L., MSN, CRNP, Hsu, Amy P., BA, Kuhns, Douglas B., PhD, Zerbe, Christa S., MD, Holland, Steven M., MD

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