Zobrazeno 1 - 10
of 295
pro vyhledávání: '"Español T"'
Publikováno v:
In Allergologia et Immunopathologia 2007 35(5):184-192
Autor:
Soler-Palacín, P., Margareto, C., Llobet, P., Asensio, O., Hernández, M., Caragol, I., Español, T.
Publikováno v:
In Allergologia et Immunopathologia 2007 35(3):83-89
Autor:
Español, T., Hernández, M., Giner, M.T., Casas, C., Gurbindo, D., Marco, T., Larramona, H., García, J.M.
Publikováno v:
In Allergologia et Immunopathologia 2005 33(3):157-161
Publikováno v:
In Allergologia et Immunopathologia 2002 30(1):42-46
Autor:
Toubiana, J., Okada, S., Hiller, J., Oleastro, M., Lagos Gomez, M., Aldave Becerra, J. C., Ouachee-Chardin, M., Fouyssac, F., Girisha, K. M., Etzioni, A., Van Montfrans, J., Camcioglu, Y., Kerns, L. A., Belohradsky, B., Blanche, S., Bousfiha, A., Rodriguez-Gallego, C., Meyts, I., Kisand, K., Reichenbach, J., Renner, E. D., Rosenzweig, S., Grimbacher, B., van de Veerdonk, F. L., Traidl-Hoffmann, C., Picard, C., Marodi, L., Morio, T., Kobayashi, M., Lilic, D., Milner, J. D., Holland, S., Casanova, J. -L., Puel A, Cypowyj S, Thumerelle C, Toulon A, Bustamante J, Tahuil N, SALHI, DALILA, Boiu S, Chopra C, Di Giovanni D, Bezrodnik L, Boutros J, Thomas C, Lacuesta G, Jannier S, Korganow AS, Paillard C, Boutboul, Bué M, Marie-Cardine A, Bayart S, Migaud M, Weiss, Karmochkine M, Garcia-Martinez JM, Stephan JL, Bensaid P, Jeannoel GP, Witte T, Baumann U, Harrer T, Navarrete C, ACOSTA HUGHES, BENJAMIN, Firinu, Pignata C, Picco P, Mendoza D, Lugo Reyes SO, Torres Lozano C, Ortega-Cisneros M, Cortina M, Mesdaghi M, Nabavi M, Español T, Martínez-Saavedra MT, Rezaei N, Zoghi S, Pac M, Barlogis V, Revon-Rivière G, Haimi-Cohen Y, Spiegel R, Miron D, Bouchaib J, Blancas-Galicia L, Toth B, Drexel B, Rohrlich PS, Lesens O, Hoernes M, Drewe E, Abinum M, Sawalle-Belohradsky J, Kindle G, Depner M, Milani L, Nikopensius T, Remm M, Talas UG, Tucker M, Willis M, Leonard S, Meuwissen H, Ferdman RM, CORBO UGULINO, WALLACE, Desai MM, Taur P, Badolato R, Soltesz B, Schnopp C, Jansson AF, Ayvaz D, Shabashova N, Chernyshova L, Bondarenko A, Moshous D, Neven B, Boubidi C, Ailal F, Giardino G, Del Giacco S, Bougnoux ME, Imai K, Okawa T, Mizoguchi Y, Ozaki Y, Takeuchi M, Hayakawa A, Lögering B, Reich K, Buhl T, Eyerich K, Schaller M, Arkwright PD, Gennery AR, Cant AJ, Warris A, Henriet S, Mekki N, Barbouche R, Ben Mustapha I, Bodemer, Polak M, Grimprel E, Burgel PR, Fischer A, Hermine O, Debré M, Kocacyk D, Dhalla F, Patel SY, Moens L, Haerynck F, Dullaers, Hoste L, Sanal O, Kilic SS, Roesler J, Lanternier F, Lortholary O, Fieschi C, Church JA, Roifman C, Yuenyongviwat A, Peterson P, Boisson-Dupuis S, Abel L, Marciano BE, Netea MG.
Publikováno v:
Blood, 127(25), 3154. American Society of Hematology
Blood, 127, 3154-64
Blood, 127, 25, pp. 3154-64
Blood, 127, 3154-64
Blood, 127, 25, pp. 3154-64
Contains fulltext : 172671.pdf (Publisher’s version ) (Closed access) Since their discovery in patients with autosomal dominant (AD) chronic mucocutaneous candidiasis (CMC) in 2011, heterozygous STAT1 gain-of-function (GOF) mutations have increasin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6a3b7f9c5e0b02e255e53b51e0bb9d0
https://doi.org/10.1182/blood-2015-11-679902
https://doi.org/10.1182/blood-2015-11-679902
Autor:
Español, T.
Publikováno v:
In Allergologia et Immunopathologia 2001 29(3):118-121
Publikováno v:
Clinical & Experimental Immunology. Dec1979, Vol. 38 Issue 3, p615-620. 6p.
Publikováno v:
In Transplantation Proceedings 2002 34(1):100-101
As imunodeficiências primárias (IDP) por défice predominante de anticorpos são as IDP mais frequentes. Apresentam fenótipos muito diversos, com espectro de manifestações clinicas muito variável que pode atrasar o diagnóstico. O seguimento de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1504::6bd8b69e396de213d105e5f1ffff85d6
https://hdl.handle.net/10400.4/1273
https://hdl.handle.net/10400.4/1273
Autor:
Allende, L M, Hernández, M, Corell, A, García-Pérez, M A, Varela, P, Moreno, A, Caragol, I, García-Martín, F, Guillén-Perales, J, Olivé, T, Español, T, Arnaiz-Villena, A
Leucocyte adhesion deficiency (LAD) is an autosomal-recessive genetic disease that is characterized clinically by severe bacterial infections and caused by mutations in the CD18 gene that codes for the beta2 integrin subunit. A patient with a severe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4da1faa60c043a8a3d5442ae030f5064
https://europepmc.org/articles/PMC2327173/
https://europepmc.org/articles/PMC2327173/