Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia

por Davies, E. Graham
Publicado 2013

Update on the hyper immunoglobulin M syndromes

por Davies, E Graham, Thrasher, Adrian J
Publicado 2010

Congenital Athymia: Unmet Needs and Practical Guidance

por Howley, Evey, Davies, E Graham, Kreins, Alexandra Y
Publicado 2023

Current and Future Therapeutic Approaches for Thymic Stromal Cell Defects

por Kreins, Alexandra Y., Bonfanti, Paola, Davies, E. Graham
Publicado 2021

Transplanted human thymus slices induce and support T‐cell development in mice after cryopreservation

por Ross, Susan, Cheung, Melissa, Lau, Ching‐In, Sebire, Neil, Burch, Michael, Kilbride, Peter, Fuller, Barry, Morris, G. John, Davies, E Graham, Crompton, Tessa
Publicado 2018

T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss

por Furmanski, Anna L, O'Shaughnessy, Ryan F L, Saldana, Jose Ignacio, Blundell, Michael P, Thrasher, Adrian J, Sebire, Neil J, Davies, E Graham, Crompton, Tessa
Publicado 2013

ADA2 deficiency complicated by EBV-driven lymphoproliferative disease

por Staples, Emily, Simeoni, Ilenia, Stephens, Jonathan C., Allen, Hana Lango, Wright, Penny, Davies, E. Graham, Javid, Babak, Gkrania-Klotsas, Effrossyni, Gattens, Michael, Firth, Helen, Shamardina, Olga, Deevi, Sri V.V., Prapa, Matina, Uttenthal, Ben, Kumararatne, Dinakantha, Thaventhiran, James E.D.
Publicado 2020

Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency()

por Hassan, Amel, Lee, Pamela, Maggina, Paraskevi, Xu, Jin Hua, Moreira, Diana, Slatter, Mary, Nademi, Zohreh, Worth, Austen, Adams, Stuart, Jones, Alison, Cale, Catherine, Allwood, Zoe, Rao, Kanchan, Chiesa, Robert, Amrolia, Persis, Gaspar, Hubert, Davies, E. Graham, Veys, Paul, Gennery, Andrew, Qasim, Waseem
Publicado 2014

Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development

por Mustillo, Peter J., Sullivan, Kathleen E., Chinn, Ivan K., Notarangelo, Luigi D., Haddad, Elie, Davies, E. Graham, de la Morena, Maria Teresa, Hartog, Nicholas, Yu, Joyce E., Hernandez-Trujillo, Vivian P., Ip, Winnie, Franco, Jose, Gambineri, Eleonora, Hickey, Scott E., Varga, Elizabeth, Markert, M. Louise
Publicado 2023

Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

por Giardino, Giuliana, Sharapova, Svetlana O., Ciznar, Peter, Dhalla, Fatima, Maragliano, Luca, Radha Rama Devi, Akella, Islamoglu, Candan, Ikinciogullari, Aydan, Haskologlu, Sule, Dogu, Figen, Hanna-Wakim, Rima, Dbaibo, Ghassan, Chou, Janet, Cirillo, Emilia, Borzacchiello, Carla, Kreins, Alexandra Y., Worth, Austen, Rota, Ioanna A., Marques, José G., Sayitoglu, Muge, Firtina, Sinem, Mahdi, Moaffaq, Geha, Raif, Neven, Bénédicte, Sousa, Ana E., Benfenati, Fabio, Hollander, Georg A., Davies, E. Graham, Pignata, Claudio
Publicado 2021

A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

por Jabara, Haifa H., Boyden, Steven E., Chou, Janet, Ramesh, Narayanaswamy, Massaad, Michel J., Benson, Halli, Bainter, Wayne, Fraulino, David, Rahimov, Fedik, Sieff, Colin, Liu, Zhi-Jian, Alshemmari, Salem H., Al-Ramadi, Basel K., Al-Dhekri, Hasan, Arnaout, Rand, Abu-Shukair, Mohammad, Vatsayan, Anant, Silver, Eli, Ahuja, Sanjay, Davies, E. Graham, Sola-Visner, Martha, Ohsumi, Toshiro K., Andrews, Nancy C., Notarangelo, Luigi D., Fleming, Mark D., Al-Herz, Waleed, Kunkel, Louis M., Geha, Raif S.
Publicado 2015

Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API)

por Speckmann, Carsten, Nennstiel, Uta, Hönig, Manfred, Albert, Michael H., Ghosh, Sujal, Schuetz, Catharina, Brockow, Inken, Hörster, Friederike, Niehues, Tim, Ehl, Stephan, Wahn, Volker, Borte, Stephan, Lehmberg, Kai, Baumann, Ulrich, Beier, Rita, Krüger, Renate, Bakhtiar, Shahrzad, Kuehl, Joern-Sven, Klemann, Christian, Kontny, Udo, Holzer, Ursula, Meinhardt, Andrea, Morbach, Henner, Naumann-Bartsch, Nora, Rothoeft, Tobias, Kreins, Alexandra Y., Davies, E. Graham, Schneider, Dominik T., Bernuth, Horst v., Klingebiel, Thomas, Hoffmann, Georg F., Schulz, Ansgar, Hauck, Fabian
Publicado 2023

Thymus transplantation for complete DiGeorge syndrome: European experience

por Davies, E. Graham, Cheung, Melissa, Gilmour, Kimberly, Maimaris, Jesmeen, Curry, Joe, Furmanski, Anna, Sebire, Neil, Halliday, Neil, Mengrelis, Konstantinos, Adams, Stuart, Bernatoniene, Jolanta, Bremner, Ronald, Browning, Michael, Devlin, Blythe, Erichsen, Hans Christian, Gaspar, H. Bobby, Hutchison, Lizzie, Ip, Winnie, Ifversen, Marianne, Leahy, T. Ronan, McCarthy, Elizabeth, Moshous, Despina, Neuling, Kim, Pac, Malgorzata, Papadopol, Alina, Parsley, Kathryn L., Poliani, Luigi, Ricciardelli, Ida, Sansom, David M., Voor, Tiia, Worth, Austen, Crompton, Tessa, Markert, M. Louise, Thrasher, Adrian J.
Publicado 2017

Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia

por Zielen, Stefan, Duecker, Ruth Pia, Woelke, Sandra, Donath, Helena, Bakhtiar, Sharhzad, Buecker, Aileen, Kreyenberg, Hermann, Huenecke, Sabine, Bader, Peter, Mahlaoui, Nizar, Ehl, Stephan, El-Helou, Sabine M., Pietrucha, Barbara, Plebani, Alessandro, van der Flier, Michiel, van Aerde, Koen, Kilic, Sara S., Reda, Shereen M., Kostyuchenko, Larysa, McDermott, Elizabeth, Galal, Nermeen, Pignata, Claudio, Pérez, Juan Luis Santos, Laws, Hans-Juergen, Niehues, Tim, Kutukculer, Necil, Seidel, Markus G., Marques, Laura, Ciznar, Peter, Edgar, John David M., Soler-Palacín, Pere, von Bernuth, Horst, Krueger, Renate, Meyts, Isabelle, Baumann, Ulrich, Kanariou, Maria, Grimbacher, Bodo, Hauck, Fabian, Graf, Dagmar, Granado, Luis Ignacio Gonzalez, Prader, Seraina, Reisli, Ismail, Slatter, Mary, Rodríguez-Gallego, Carlos, Arkwright, Peter D., Bethune, Claire, Deripapa, Elena, Sharapova, Svetlana O., Lehmberg, Kai, Davies, E. Graham, Schuetz, Catharina, Kindle, Gerhard, Schubert, Ralf
Publicado 2021

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases

por Pagnamenta, Alistair T., Camps, Carme, Giacopuzzi, Edoardo, Taylor, John M., Hashim, Mona, Calpena, Eduardo, Kaisaki, Pamela J., Hashimoto, Akiko, Yu, Jing, Sanders, Edward, Schwessinger, Ron, Hughes, Jim R., Lunter, Gerton, Dreau, Helene, Ferla, Matteo, Lange, Lukas, Kesim, Yesim, Ragoussis, Vassilis, Vavoulis, Dimitrios V., Allroggen, Holger, Ansorge, Olaf, Babbs, Christian, Banka, Siddharth, Baños-Piñero, Benito, Beeson, David, Ben-Ami, Tal, Bennett, David L., Bento, Celeste, Blair, Edward, Brasch-Andersen, Charlotte, Bull, Katherine R., Cario, Holger, Cilliers, Deirdre, Conti, Valerio, Davies, E. Graham, Dhalla, Fatima, Dacal, Beatriz Diez, Dong, Yin, Dunford, James E., Guerrini, Renzo, Harris, Adrian L., Hartley, Jane, Hollander, Georg, Javaid, Kassim, Kane, Maureen, Kelly, Deirdre, Kelly, Dominic, Knight, Samantha J. L., Kreins, Alexandra Y., Kvikstad, Erika M., Langman, Craig B., Lester, Tracy, Lines, Kate E., Lord, Simon R., Lu, Xin, Mansour, Sahar, Manzur, Adnan, Maroofian, Reza, Marsden, Brian, Mason, Joanne, McGowan, Simon J., Mei, Davide, Mlcochova, Hana, Murakami, Yoshiko, Németh, Andrea H., Okoli, Steven, Ormondroyd, Elizabeth, Ousager, Lilian Bomme, Palace, Jacqueline, Patel, Smita Y., Pentony, Melissa M., Pugh, Chris, Rad, Aboulfazl, Ramesh, Archana, Riva, Simone G., Roberts, Irene, Roy, Noémi, Salminen, Outi, Schilling, Kyleen D., Scott, Caroline, Sen, Arjune, Smith, Conrad, Stevenson, Mark, Thakker, Rajesh V., Twigg, Stephen R. F., Uhlig, Holm H., van Wijk, Richard, Vona, Barbara, Wall, Steven, Wang, Jing, Watkins, Hugh, Zak, Jaroslav, Schuh, Anna H., Kini, Usha, Wilkie, Andrew O. M., Popitsch, Niko, Taylor, Jenny C.
Publicado 2023