Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Hacein-Bey S"'
Autor:
Nocturne, G. (1), Ly, B. (2), Boudaoud, S. (3), Seror, R. (4), Nicco, C. (5), Chereau, C. (5), Kavian, N. (5), Batteux, F. (6), Mackay, F. (7), Vincent, F. (7), Lazure, T. (8), Krzysiek, R. (9), Hacein-Bey, S. (9), Stimmer, L. (10), Ferlicot, S. (8), Mariette, X. (11)
Publikováno v:
In Revue du rhumatisme November 2016 83 Supplement 1:A235-A236
Autor:
Bitoun, S., Hassler, S., Szely, N., Gleizes, A., Hacein Bey, S., Richez, C., Soubrier, M., Avouac, J., Brocq, O., Sellam, J., De Vries, N., Huizinga, T.W., Jury, E., Manson, J., Mauri, C., Mattuci, A., Bröet, P., Mariette, X.
Publikováno v:
In Revue du rhumatisme December 2022 89 Supplement 1:A21-A22
Autor:
Lavaud, J., Chrétien, P., Deschamps, L., Hacein-Bey, S., Descamps, V., Mignot, S., Maxime, B., Psimaras, D., Brunet Possenti, F.
Publikováno v:
In Annales de Dermatologie et de Vénéréologie - FMC November 2022 2(8) Supplement 1:A174-A175
Autor:
Fischer, A., Hacein-Bey, S., Le Deist, F., de Saint Basile, G., de Villartay, JP, Cavazzana-Calvo, M.
Publikováno v:
In Journal de pediatrie et de puericulture 2002 15(1):4-10
Autor:
Bitoun, S., Ly, B., Hassler, S., Paoletti, A., Gleizes, A., Hacein Bey, S., Bröet, P., Pallardy, M., Mariette, X.
Publikováno v:
In Revue du rhumatisme December 2021 88 Supplement 1:A134-A135
Autor:
Fernandes, Jf, Rocha, V, Labopin, M, Neven, B, Moshous, D, Gennery, Ar, Friedrich, W, Porta, F, Diaz de Heredia, C, Wall, D, Bertrand, Y, Veys, P, Slatter, M, Schulz, A, Chan, Kw, Grimley, M, Ayas, M, Gungor, T, Ebell, W, Bonfim, C, Kalwak, K, Taupin, P, Blanche, S, Gaspar, Hb, Landais, P, Fischer, A, Gluckman, E, Cavazzana Calvo, M, Eurocord, Inborn Errors Working Party of European Group for Blood, Marrow Transplantation: Ahmed, A, Auiti, A, Biffi, A, Cant, A, Fasth, A, Gennery, A, Hassan, A, Lankester, A, O'Mera, A, Plabani, A, Rovelli, A, Salmon, A, Scarselli, A, Thrasher, A, Van Royen, A, Villa, A, Wawer, A, Wahadneh, A, Worth, A, Belohradsky, B, Wolska, B, Gaspar, B, Bonfirm, C, Booth, C, Klein, C, Messina, C, Peters, C, Steward, C, Lindemans, C, Schuetz, C, de Heredia Rubio CD, Bensoussan, D, Gleadow, D, Lilic, D, Gambineri, Eleonora, Smith, E, Aerts, F, Caracseghi, F, Roberts, G, Davies, G, Al Mousa, H, Jossanc, H, Ozsahim, H, Hirsch, I, Meyts, I, Tezcan, I, Mueller, I, Andresc, I, Boelens, J, Fernandes, J, Folloni, J, Keuhl, J, Reichenbach, J, Stary, J, Wachowiak, J, Xu Bayford, J, Cunha, Jm, Ehlert, J, Rao, K, Sykora, K, Andais, L, Brown, L, Dal Cortivo, L, Griffith, L, Notarangelo, L, Abinun, M, Albert, M, Bierings, M, Bouchet, M, Cavazzana, M, Hirschfield, M, Cowan, M, Hoenig, M, Loubser, M, Roncarolo, M, Sauer, M, Schneider, M, Verstegen, M, Schroeder, M, Essink, M, Yesilipek, M, Entz Werle, N, Mahlaoui, N, Schlautmann, N, Taylor, N, Vanroyen, N, Walffraat, N, Sanal, O, Amrolia, P, Bordigoni, P, De Coppi, P, Frange, P, Orchard, P, Sedlacek, P, Shaw, P, Stephensky, P, Bacchetta, R, Bredius, R, Formankova, R, Gale, R, Seger, R, Wynn, R, Corbacioglu, S, Ehl, S, Hacein Bey, S, Hambleton, S, Mohsen, S, Mueller, S, Pai, Sy, Espanol, T, Flood, T, Guengoer, T, Bordon, V, Ormoor, V, Pashano, V, Courteille, V, Czogala, W, Qasim, W, Camci, Y, Nademi, Z.
Publikováno v:
Blood, 119(12), 2949-2955
Pediatric patients with SCID constitute medical emergencies. In the absence of an HLA-identical hematopoietic stem cell (HSC) donor, mismatched related-donor transplantation (MMRDT) or unrelated-donor umbilical cord blood transplantation (UCBT) are v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dec6b3b56c93759ab790c3b03bb80968
https://hdl.handle.net/1887/98304
https://hdl.handle.net/1887/98304
Autor:
André-Schmutz, I, Le Deist, F, Hacein-Bey, S, Hamel, Y, Vitetta, E, Schindler, J, Fischer, A, Cavazzana-Calvo, M
Publikováno v:
In Transplantation Proceedings 2002 34(7):2927-2928
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781461351948
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83cf35f7bfa77bf0a9e4a158f4f5f4e9
https://doi.org/10.1007/978-1-4615-0685-0_27
https://doi.org/10.1007/978-1-4615-0685-0_27
Publikováno v:
Europe PubMed Central
X-linked severe combined immunodeficiency (SCID-Xl) is a rare human inherited disorder in which early T and natural killer (NK) lymphocyte development is blocked. The genetic disorder results from mutations in the common gammac chain that participate
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