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Publications by Neven, Benedicte

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Number of items: 8.

Journal article

Aydin, Susanne E.; Freeman, Alexandra F.; Al-Herz, Waleed; Al-Mousa, Hamoud A.; Arnaout, Rand K.; Aydin, Roland C.; Barlogis, Vincent; Belohradsky, Bernd H.; Bonfim, Carmem; Bredius, Robbert G.; Chu, Julia I.; Ciocarlie, Oana C.; Dogu, Figen; Gaspar, Hubert B.; Geha, Raif S.; Gennery, Andrew R.; Hauck, Fabian; Hawwari, Abbas; Hickstein, Dennis D.; Hönig, Manfred; Ikinciogullari, Aydan; Klein, Christoph; Kumar, Ashish; Ifversen, Marianne R. S.; Matthes, Susanne; Metin, Ayse; Neven, Benedicte; Pai, Sung-Yun; Parikh, Suhag H.; Picard, Capucine; Renner, Ellen D.; Sanal, Özden; Schulz, Ansgar S.; Schuster, Friedhelm; Shah, Nirali N.; Shereck, Evan B.; Slatter, Mary A.; Su, Helen C.; Montfrans, Joris van; Woessmann, Wilhelm; Ziegler, John B.; Albert, Michael H. (2018): Hematopoietic stem cell transplantation as treatment for patients with DOCK8 deficiency. In: Journal of Allergy and Clinical Immunology

Vanoni, Federica; Caorsi, Roberta; Aeby, Sandra; Cochard, Marie; Anton, Jordi; Berg, Stefan; Brik, Riva; Dolezalova, Pavla; Kone-Paut, Isabelle; Neven, Benedicte; Ozen, Seza; Pillet, Pascal; Stojanov, Silvia; Wouters, Carine; Gattorno, Marco; Hofer, Michael (2018): Towards a new set of classification criteria for PFAPA syndrome. In: Pediatric Rheumatology 16:60 [PDF, 533kB]

Barzaghi, Federica; Hernandez, Laura Cristina Amaya; Neven, Benedicte; Ricci, Silvia; Kucuk, Zeynep Yesim; Bleesing, Jack J.; Nademi, Zohreh; Slatter, Mary Anne; Ulloa, Erlinda Rose; Shcherbina, Anna; Roppelt, Anna; Worth, Austen; Silva, Juliana; Aiuti, Alessandro; Murguia-Favela, Luis; Speckmann, Carsten; Carneiro-Sampaio, Magda; Fernandes, Juliana Folloni; Baris, Safa; Ozen, Ahmet; Karakoc-Aydiner, Elif; Kiykim, Ayca; Schulz, Ansgar; Steinmann, Sandra; Notarangelo, Lucia Dora; Gambineri, Eleonora; Lionetti, Paolo; Shearer, William Thomas; Forbes, Lisa R.; Martinez, Caridad; Moshous, Despina; Blanche, Stephane; Fisher, Alain; Ruemmele, Frank M.; Tissandier, Come; Ouachee-Chardin, Marie; Rieux-Laucat, Frederic; Cavazzana, Marina; Qasim, Waseem; Lucarelli, Barbarella; Albert, Michael H.; Kobayashi, Ichiro; Alonso, Laura; De Heredia, Cristina Diaz; Kanegane, Hirokazu; Lawitschka, Anita; Seo, Jong Jin; Gonzalez-Vicent, Marta; Diaz, Miguel Angel; Goyal, Rakesh Kumar; Sauer, Martin G.; Yesilipek, Akif; Kim, Minsoo; Yilmaz-Demirdag, Yesim; Bhatia, Monica; Khlevner, Julie; Padilla, Erick J. Richmond; Martino, Silvana; Montin, Davide; Neth, Olaf; Molinos-Quintana, Agueda; Valverde-Fernandez, Justo; Broides, Arnon; Pinsk, Vered; Ballauf, Antje; Haerynck, Filomeen; Bordon, Victoria; Dhooge, Catharina; Garcia-Lloret, Maria Laura; Bredius, Robbert G.; Kawak, Krzysztof; Haddad, Elie; Seidel, Markus Gerhard; Duckers, Gregor; Pai, Sung-Yun; Dvorak, Christopher C.; Ehl, Stephan; Locatelli, Franco; Goldman, Frederick; Gennery, Andrew Richard; Cowan, Mort J.; Roncarolo, Maria-Grazia; Bacchetta, Rosa (2018): Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study. In: Journal of Allergy and Clinical Immunology, Vol. 141, No. 3: pp. 1036-1049

Bomken, Simon; Werff Ten Bosch, Jutte van der; Attarbaschi, Andishe; Bacon, Chris M.; Borkhardt, Arndt; Boztug, Kaan; Fischer, Ute; Hauck, Fabian; Kuiper, Roland P.; Lammens, Tim; Loeffen, Jan; Neven, Benedicte; Pan-Hammarstrom, Qiang; Quinti, Isabella; Seidel, Markus G.; Warnatz, Klaus; Wehr, Claudia; Lankester, Arjan C.; Gennery, Andrew R. (2018): Current Understanding and Future Research Priorities in Malignancy Associated With Inborn Errors of Immunity and DNA Repair Disorders: The Perspective of an Interdisciplinary Working Group. In: Frontiers in Immunology, Vol. 9, 2912 [PDF, 803kB]

Speckmann, Carsten; Doerken, Sam; Aiuti, Alessandro; Albert, Michael H.; Al-Herz, Waleed; Allende, Luis M.; Scarselli, Alessia; Avcin, Tadej; Perez-Becker, Ruy; Cancrini, Caterina; Cant, Andrew; Cesare, Silvia di; Finocchi, Andrea; Fischer, Alain; Gaspar, H. Bobby; Ghosh, Sujal; Gennery, Andrew; Gilmour, Kimberly; Gonzalez-Granado, Luis I.; Martinez-Gallo, Monica; Hambleton, Sophie; Hauck, Fabian; Hoenig, Manfred; Moshous, Despina; Neven, Benedicte; Niehues, Tim; Notarangelo, Luigi; Picard, Capucine; Rieber, Nikolaus; Schulz, Ansgar; Schwarz, Klaus; Seidel, Markus G.; Soler-Palacin, Pere; Stepensky, Polina; Strahm, Brigitte; Vraetz, Thomas; Warnatz, Klaus; Winterhalter, Christine; Worth, Austen; Fuchs, Sebastian; Uhlmann, Annette; Ehl, Stephan (2017): A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis. In: Journal of Allergy and Clinical Immunology, Vol. 139, No. 4: pp. 1302-1310

Toubiana, Julie; Okada, Satoshi; Hiller, Julia; Oleastro, Matias; Lagos Gomez, Macarena; Aldave Becerra, Juan Carlos; Ouachée-Chardin, Marie; Fouyssac, Fanny; Girisha, Katta Mohan; Etzioni, Amos; Montfrans, Joris van; Camcioglu, Yildiz; Kerns, Leigh Ann; Belohradsky, Bernd; Blanche, Stéphane; Bousfiha, Aziz; Rodriguez-Gallego, Carlos; Meyts, Isabelle; Kisand, Kai; Reichenbach, Janine; Renner, Ellen D.; Rosenzweig, Sergio; Grimbacher, Bodo; Veerdonk, Frank L. van de; Traidl-Hoffmann, Claudia; Picard, Capucine; Marodi, Laszlo; Morio, Tomohiro; Kobayashi, Masao; Lilic, Desa; Milner, Joshua D.; Holland, Steven; Casanova, Jean-Laurent; Puel, Anne; Cypowyj, Sophie; Thumerelle, Caroline; Toulon, Antoine; Bustamante, Jacinta; Tahuil, Natalia; Salhi, Aicha; Boiu, Sorina; Chopra, Charu; Di Giovanni, Daniela; Bezrodnik, Liliana; Boutros, Jeannette; Thomas, Caroline; Lacuesta, Gina; Jannier, Sarah; Korganow, Anne-Sophie; Paillard, Catherine; Boutboul, David; Bue, Melanie; Marie-Cardine, Aude; Bayart, Sophie; Migaud, Melanie; Weiss, Laurence; Karmochkine, Marina; Garcia-Martinez, Juan-Miguel; Stephan, Jean-Louis; Bensaid, Philippe; Jaennoel, Guy-Patrick; Witte, Torsten; Baumann, Ulrich; Harrer, Thomas; Navarrete, Carmen; Benjamin, Antony Terance; Firinu, Davide; Pignata, Claudio; Picco, Paolo; Mendoza, David; Reyes, Saul Oswaldo Lugo; Lozano, Carlos Torres; Ortega-Cisneros, Margarita; Cortina, Mariana; Mesdaghi, Mehrnaz; Nabavi, Mohammad; Espanol, Teresa; Martinez-Saavedra, Maia Teresa; Rezaei, Nima; Zoghi, Samaneh; Pac, Malgorzata; Barlogis, Vincent; Revon-Riviere, Gabriel; Haimi-Cohen, Yishai; Spiegel, Ronen; Miron, Dan; Bouchaib, Jabir; Blancas-Galicia, Lizbeth; Toth, Beata; Drexel, Barbara; Rohrlich, Pierre Simon; Lesens, Olivier; Hoernes, Miriam; Drewe, Elizabeth; Abinum, Mario; Sawalle-Belohradsky, Julie; Kindle, Gerhard; Depner, Mark; Milani, Lili; Nikopensius, Tiit; Remm, Maido; Talas, Ulvi Gerst; Tucker, Mark; Willis, Mary; Leonard, Stephanie; Meuwissen, Hilaire; Ferdman, Ronald M.; Wallace, Mark; Desai, Mukesh M.; Taur, Prasad; Badolato, Raffaele; Soltesz, Beata; Schnopp, Christina; Jansson, Annette F.; Ayvaz, Deniz; Shabashova, Nadejda; Chernyshova, Liudmyla; Bondarenko, Anastasia; Moshous, Despina; Neven, Benedicte; Boubidi, Chahinez; Ailal, Fatima; Giardino, Giuliana; Del Giacco, Stefano; Bougnoux, Marie-Elisabeth; Imai, Kohsuke; Okawa, Teppei; Mizoguchi, Yoko; Ozaki, Yusuke; Takeuchi, Masato; Hayakawa, Akira; Logering, Birgit; Reich, Kristian; Buhl, Timo; Eyerich, Kilian; Schaller, Martin; Arkwright, Peter D.; Gennery, Andrew R.; Cant, Andrew J.; Warris, Adilia; Henriet, Stefanie; Mekki, Najla; Barbouche, Ridha; Ben Mustapha, Imen; Bodemer, Christine; Polak, Michel; Grimprel, Emmanuel; Burgel, Pierre-Regis; Fischer, Alain; Hermine, Olivier; Debre, Marianne; Kocacyk, Dilara; Dhalla, Fatima; Patel, Smita Y.; Moens, Leen; Haerynck, Filomeen; Dullaers, Melissa; Hoste, Levi; Sanal, Ozden; Kilic, Sara Sebnem; Roesler, Joachim; Lanternier, Fanny; Lortholary, Olivier; Fieschi, Claire; Church, Joseph A.; Roifman, Chaim; Yuenyongviwat, Araya; Peterson, Part; Boisson-Dupuis, Stephanie; Abel, Laurent; Marciano, Beatriz E.; Netea, Mihai G. (2016): Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. In: Blood, Vol. 127, No. 25: pp. 3154-3164

Aydin, Susanne; Freeman, Alexandra F.; Su, Helen; Hickstein, Dennis; Pai, Sung-Yun; Geha, Raif; Chatila, Talal; Arnaout, Rand K.; Al-Mousa, Hamoud; Al-Dhekri, Hasan; Renner, Ellen D.; Belohradsky, Bernd H.; Notheis, Gundula; Aydin, Roland; Gaspar, Bobby H.; Al-Herz, Waleed; Gennery, Andrew; Slatter, Mary; Metin, Ayse; Isik, Pamir; Azik, Fatih; Ikinciogullari, Aydan; Haskologlu, Sule; Dogu, Figen; Kumar, Ashish; Ifversen, Marianne; Schuster, Friedhelm; Woessmann, Wilhelm; Bredius, Robbert; Barlogis, Vincent; Kainulainen, Leena; Picard, Capucine; Neven, Benedicte; Shereck, Evan; Schulz, Ansgar; Dueckers, Gregor; Montfrans, Joris van; Matthes-Martin, Susanne; Keles, Sevgi; Ochs, Hans; Albert, Michael H. (2016): HSCT for DOCK8 Deficiency - an International Study on 74 Patients. In: Biology of Blood and Marrow Transplantation, Vol. 22, No. 3: S103-S104

Toplak, Natasa; Frenkel, Joost; Ozen, Seza; Lachmann, Helen J.; Woo, Patricia; Koné-Paut, Isabelle; De Benedetti, Fabrizio; Neven, Benedicte; Hofer, Michael; Dolezalova, Pavla; Kümmerle-Deschner, Jasmin; Touitou, Isabelle; Hentgen, Veronique; Simon, Anna; Girschick, Herman; Rose, Carlos; Wouters, Carine; Vesely, Richard; Arostegui, Juan; Stojanov, Silvia; Ozgodan, Huri; Martini, Alberto; Ruperto, Nicolino; Gattorno, Marco (July 2012): An international registry on autoinflammatory diseases: the Eurofever experience. In: Annals of the rheumatic diseases, Vol. 71, No. 7: pp. 1177-1182 [PDF, 225kB]

This list was generated on Thu Apr 22 01:55:46 2021 CEST.