Myeloid dysplasia and bone marrow hypocellularity in adenosine deaminase-deficient severe combined immune deficiency

Por Sokolic, Robert, Maric, Irina, Kesserwan, Chimene, Garabedian, Elizabeth, Hanson, I. Celine, Dodds, Margaret, Buckley, Rebecca, Issekutz, Andrew C., Kamani, Naynesh, Shaw, Kit, Tan, Ben, Bali, Pawan, Hershfield, Michael S., Kohn, Donald B., Wayne, Alan S., Candotti, Fabio
Publicado em 2011

Rapid Genetic Analysis of X-Linked Chronic Granulomatous Disease by High-Resolution Melting

Por Hill, Harry R., Augustine, Nancy H., Pryor, Robert J., Reed, Gudrun H., Bagnato, Joshua D., Tebo, Anne E., Bender, Jeffrey M., Pasi, Brian M., Chinen, Javier, Hanson, I. Celine, de Boer, Martin, Roos, Dirk, Wittwer, Carl T.
Publicado em 2010

Hematopoietic Stem Cell Transplantation for CD3δ deficiency

Por Marcus, Nufar, Takada, Hidetoshi, Law, Jason, Cowan, Morton J, Gil, Juana, Regueiro, Jose, Lopez de Sabando, Diego Plaza, Lopez-Granados, Eduardo, Dalal, Jignesh, Friedrich, Wilhelm, Manfred, Hoenig, Hanson, I. Celine, Grunebaum, Eyal, Shearer, William T, Roifman, Chaim M.
Publicado no J Allergy Clin Immunol (2011)

Outcomes of Severe Combined Immunodeficiency Patients Treated with Hematopoietic Stem Cell Transplantation with and without Pre-conditioning

Por Patel, Niraj C., Chinen, Javier, Rosenblatt, Howard M., Hanson, I. Celine, Krance, Robert A., Paul, Mary E., Abramson, Stuart L., Noroski, Lenora M., Davis, Carla M., Seeborg, Filiz O., Foster, Samuel B., Leung, Kathryn S., Brown, Betty S., Ritz, Jerome, Shearer, William T.
Publicado em 2009

Frequent Detection of Escape from Cytotoxic T-Lymphocyte Recognition in Perinatal Human Immunodeficiency Virus (HIV) Type 1 Transmission: the Ariel Project for the Prevention of...

Por Wilson, Cara C., Brown, R. Clark, Korber, Bette T., Wilkes, Barbara M., Ruhl, Debbie J., Sakamoto, Doreen, Kunstman, Kevin, Luzuriaga, Katherine, Hanson, I. Celine, Widmayer, Susan M., Wiznia, Andrew, Clapp, Sheila, Ammann, Arthur J., Koup, Richard A., Wolinsky, Steven M., Walker, Bruce D.
Publicado em 1999

Somatic reversion in DOCK8 immunodeficiency modulates disease phenotype

Por Jing, Huie, Zhang, Qian, Zhang, Yu, Hill, Brenna J., Dove, Christopher G., Gelfand, Erwin W., Atkinson, T. Prescott, Uzel, Gulbu, Matthews, Helen F., Mustillo, Peter J., Lewis, David B., Kavadas, Fotini D., Hanson, I. Celine, Kumar, Ashish R., Geha, Raif S., Douek, Daniel C., Holland, Steven M., Freeman, Alexandra F., Su, Helen C.
Publicado em 2014

Next Generation Sequencing Reveals Skewing of the T and B Cell Receptor Repertoires in Patients with Wiskott–Aldrich Syndrome

Por O’Connell, Amy E., Volpi, Stefano, Dobbs, Kerry, Fiorini, Claudia, Tsitsikov, Erdyni, de Boer, Helen, Barlan, Isil B., Despotovic, Jenny M., Espinosa-Rosales, Francisco J., Hanson, I. Celine, Kanariou, Maria G., Martínez-Beckerat, Roxana, Mayorga-Sirera, Alvaro, Mejia-Carvajal, Carmen, Radwan, Nesrine, Weiss, Aaron R., Pai, Sung-Yun, Lee, Yu Nee, Notarangelo, Luigi D.
Publicado em 2014

Adoptive Immunotherapy for Primary Immunodeficiency Disorders with Virus-Specific T-lymphocytes

Por Naik, Swati, Nicholas, Sarah K, Martinez, Caridad A, Leen, Ann M, Hanley, Patrick J, Gottschalk, Steven M, Rooney, Cliona M, Hanson, I Celine, Krance, Robert A, Cruz, Conrad R, Amrolia, Persis, Lucchini, Giovanna, Bunin, Nancy, Heimall, Jennifer, Klein, Orly R, Gennery, Andrew R, Slatter, Mary A, Vickers, Mark A, Orange, Jordan S, Heslop, Helen E, Bollard, Catherine M, Keller, Michael D
Publicado no J Allergy Clin Immunol (2016)

The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospecti...

Por Dvorak, Christopher C., Cowan, Morton J., Logan, Brent R., Notarangelo, Luigi D., Griffith, Linda M., Puck, Jennifer M., Kohn, Donald B., Shearer, William T., O'Reilly, Richard J., Fleisher, Thomas A., Pai, Sung-Yun, Hanson, I. Celine, Pulsipher, Michael A., Fuleihan, Ramsay, Filipovich, Alexandra, Goldman, Frederick, Kapoor, Neena, Small, Trudy, Smith, Angela, Chan, Ka-Wah, Cuvelier, Geoff, Heimall, Jennifer, Knutsen, Alan, Loechelt, Brett, Moore, Theodore, Buckley, Rebecca H.
Publicado em 2013

PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia

Por Stray-Pedersen, Asbjørg, Backe, Paul H., Sorte, Hanne S., Mørkrid, Lars, Chokshi, Niti Y., Erichsen, Hans Christian, Gambin, Tomasz, Elgstøen, Katja B.P., Bjørås, Magnar, Wlodarski, Marcin W., Krüger, Marcus, Jhangiani, Shalini N., Muzny, Donna M., Patel, Ankita, Raymond, Kimiyo M., Sasa, Ghadir S., Krance, Robert A., Martinez, Caridad A., Abraham, Shirley M., Speckmann, Carsten, Ehl, Stephan, Hall, Patricia, Forbes, Lisa R., Merckoll, Else, Westvik, Jostein, Nishimura, Gen, Rustad, Cecilie F., Abrahamsen, Tore G., Rønnestad, Arild, Osnes, Liv T., Egeland, Torstein, Rødningen, Olaug K., Beck, Christine R., Boerwinkle, Eric A., Gibbs, Richard A., Lupski, James R., Orange, Jordan S., Lausch, Ekkehart, Hanson, I. Celine
Publicado em 2014

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

Por Booth, Claire, Gilmour, Kimberly C., Veys, Paul, Gennery, Andrew R., Slatter, Mary A., Chapel, Helen, Heath, Paul T., Steward, Colin G., Smith, Owen, O'Meara, Anna, Kerrigan, Hilary, Mahlaoui, Nizar, Cavazzana-Calvo, Marina, Fischer, Alain, Moshous, Despina, Blanche, Stephane, Pachlopnick-Schmid, Jana, Latour, Sylvain, de Saint-Basile, Genevieve, Albert, Michael, Notheis, Gundula, Rieber, Nikolaus, Strahm, Brigitte, Ritterbusch, Henrike, Lankester, Arjan, Hartwig, Nico G., Meyts, Isabelle, Plebani, Alessandro, Soresina, Annarosa, Finocchi, Andrea, Pignata, Claudio, Cirillo, Emilia, Bonanomi, Sonia, Peters, Christina, Kalwak, Krzysztof, Pasic, Srdjan, Sedlacek, Petr, Jazbec, Janez, Kanegane, Hirokazu, Nichols, Kim E., Hanson, I. Celine, Kapoor, Neena, Haddad, Elie, Cowan, Morton, Choo, Sharon, Smart, Joanne, Arkwright, Peter D., Gaspar, Hubert B.
Publicado em 2011

Primary immunodeficiency diseases – genomic approaches delineate heterogeneous Mendelian disorders

Por Stray-Pedersen, Asbjørg, Sorte, Hanne Sørmo, Samarakoon, Pubudu, Gambin, Tomasz, Chinn, Ivan K., Akdemir, Zeynep H. Coban, Erichsen, Hans Christian, Forbes, Lisa R., Gu, Shen, Yuan, Bo, Jhangiani, Shalini N., Muzny, Donna M., Rødningen, Olaug Kristin, Sheng, Ying, Nicholas, Sarah K., Noroski, Lenora M., Seeborg, Filiz O., Davis, Carla, Canter, Debra, Mace, Emily M., Vece, Tim, Allen, Carl E., Abhyankar, Harshal A., Boone, Phil, Beck, Christine R., Wiszniewski, Wojciech Krysztof, Fevang, Børre, Aukrust, Pål, Tjønnfjord, Geir E, Gedde-Dahl, Tobias, Hjorth-Hansen, Henrik, Dybedal, Ingunn, Nordøy, Ingvild, Jørgensen, Silje F., Abrahamsen, Tore G., Øverland, Torstein, Bechensteen, Anne Grete, Skogen, Vegard, Osnes, Liv T., Kulseth, Mari Ann, Prescott, Trine E., Rustad, Cecilie F., Heimdal, Ketil R., Belmont, John W., Rider, Nicholas, Chinen, Javier, Cao, Tram, Smith, Eric, Caldirola, Maria Soledad, Bezrodnik, Liliana, Reyes, Saul Oswaldo Lugo, Rosales, Francisco J. Espinosa, Guerrero, Denisse, Pedroza, Luis Alberto, Poli, Cecilia M., Franco, Jose L., Vargas, Claudia M. Trujillo, Becerra, Juan Carlos Aldave, Wright, Nicola, Issekutz, Thomas B., Issekutz, Andrew C., Abbott, Jordan, Caldwell, Jason W., Bayer, Diana K., Chan, Alice Y., Aiuti, Alessandro, Cancrini, Caterina, Holmberg, Eva, West, Christina, Burstedt, Magnus, Karaca, Ender, Yesil, Gozde, Artac, Hasibe, Bayram, Yavuz, Atik, Mehmed Musa, Eldomery, Mohammad K., Ehlayel, Mohammad S., Jolles, Stephen, Flatø, Berit, Bertuch, Alison A., Hanson, I. Celine, Zhang, Victor W., Wong, Lee-Jun, Hu, Jianhong, Walkiewicz, Magdalena, Yang, Yaping, Eng, Christine, Boerwinkle, Eric, Gibbs, Richard A., Shearer, William T., Lyle, Robert, Orange, Jordan S., Lupski, James R.
Publicado no J Allergy Clin Immunol (2016)