Zobrazeno 1 - 10
of 894
pro vyhledávání: '"Bangs, C."'
Autor:
Shillitoe, B.1,2,3, Bangs, C.1,4, Guzman, D.1,5, Gennery, A. R.1,2,3, Longhurst, H. J.6, Slatter, M.2,3, Edgar, D. M.7, Thomas, M.8, Worth, A.1,9, Huissoon, A.10, Arkwright, P. D.4, Jolles, S.11, Bourne, H.12, Alachkar, H.13, Savic, S.14, Kumararatne, D. S.6, Patel, S.15, Baxendale, H.16, Noorani, S.17, Yong, P. F. K.18
Publikováno v:
Clinical & Experimental Immunology. Jun2018, Vol. 192 Issue 3, p284-291. 9p. 3 Charts, 3 Graphs, 1 Map.
Autor:
Stubbs, A.1, Bangs, C.1,2, Shillitoe, B.3, Edgar, J. D.2,4, Burns, S. O.5, Thomas, M.6, Alachkar, H.7, Buckland, M.2,8, McDermott, E.9, Arumugakani, G.10, Jolles, M. S.11, Herriot, R.12, Arkwright, P. D.1 peter.arkwright@nhs.net
Publikováno v:
Clinical & Experimental Immunology. Feb2018, Vol. 191 Issue 2, p212-219. 8p. 3 Charts, 2 Graphs.
Akademický článek
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Autor:
Caballero, T., Aberer, W., Longhurst, H.J., Maurer, M., Zanichelli, A., Perrin, A., Bouillet, L., Andresen, I., Arcoleo, F., Bova, M., Cicardi, M., Cillari, E., Montinaro, V., Marone, G., Blanchard Delauny, C., Boccon‐Gibod, I., Coppere, B., Dzviga, C., Fain, O., Goichot, B., Gompel, A., Guez, S., Jeandel, P.Y., Kanny, G., Launay, D., Maillard, H., Martin, L., Masseau, A., Ollivier, Y., Magerl, M., Baeza, M.L., Cabañas, R., Guilarte, M., Hernández, D., Hernando de Larramendi, C., Lleonart, R., Lobera, T., Marqués, L., Bangs, C., Buckland, M., Grigoriadou, S., Helbert, M., Lorenzo, L.
Publikováno v:
Journal of the European Academy of Dermatology and Venereology
Background Hereditary angioedema (HAE) due to C1-inhibitor deficiency (C1-INH-HAE) is a rare, potentially fatal, bradykinin-mediated disease. Icatibant is a bradykinin B2 receptor antagonist originally approved in 2008 in the European Union and 2011
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab80520f2ce9abcbedb798b9d27f0e1b
http://hdl.handle.net/11588/702401
http://hdl.handle.net/11588/702401
Autor:
Maccari, M.E., Abolhassani, H., Aghamohammadi, A., Aiuti, A., Aleinikova, O., Bangs, C., Baris, S., Barzaghi, F., Baxendale, H., Buckland, M., Burns, S.O., Cancrini, C., Cant, A., Cathebras, P., Cavazzana, M., Chandra, A., Conti, F., Coulter, T., Devlin, L.A., Edgar, J.D.M., Faust, S., Fischer, A., Prat, M.G., Hammarstrom, L., Heeg, M., Jolles, S., Karakoc-Aydiner, E., Kindle, G., Kiykim, A., Kumararatne, D., Grimbacher, B., Longhurst, H., Mahlaoui, N., Milota, T., Moreira, F., Moshous, D., Mukhina, A., Neth, O., Neven, B., Nieters, A., Olbrich, P., Ozen, A., Schmid, J.P., Picard, C., Prader, S., Rae, W., Reichenbach, J., Rusch, S., Savic, S., Scarselli, A., Scheible, R., Sediva, A., Sharapova, S.O., Shcherbina, A., Slatter, M., Soler-Palacin, P., Stanislas, A., Suarez, F., Tucci, F., Uhlmann, A., van Montfrans, J., Warnatz, K., Williams, A.P., Wood, P., Kracker, S., Condliffe, A.M., Ehl, S.
Activated phosphoinositide 3-kinase (PI3K) δ Syndrome (APDS), caused by autosomal\ud dominant mutations in PIK3CD (APDS1) or PIK3R1 (APDS2), is a heterogeneous primary\ud immunodeficiency. While initial cohort-descriptions summarized the spectrum of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::9225d0cbcc12c4749f73c56bb7637be5
https://eprints.whiterose.ac.uk/129346/1/maccarifimmu-09-00543-1.pdf
https://eprints.whiterose.ac.uk/129346/1/maccarifimmu-09-00543-1.pdf
Publikováno v:
Vox Sanguinis. Apr2016, Vol. 110 Issue 3, p282-284. 3p. 2 Charts.
Autor:
Phillips, Christine1 (AUTHOR), Parkinson, Anne2 (AUTHOR) anne.parkinson@anu.edu.au, Namsrai, Tergel2 (AUTHOR), Chalmers, Anita2,3 (AUTHOR), Dews, Carolyn2,4 (AUTHOR), Gregory, Dianne2,5 (AUTHOR), Kelly, Elaine2,5 (AUTHOR), Lowe, Christine2,4 (AUTHOR), Desborough, Jane2 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 8/14/2024, Vol. 19 Issue 1, p1-10. 10p.
Autor:
Murphy, Marie1 (AUTHOR) m.murphy.3@bham.ac.uk, Coffey, Alice2 (AUTHOR), Pallan, Miranda1 (AUTHOR), Oyebode, Oyinlola3 (AUTHOR)
Publikováno v:
BMC Public Health. 7/23/2024, Vol. 24 Issue 1, p1-13. 13p.
Autor:
Gathmann B., Binder N., Ehl S., Kindle G., Mahlaoui N., Devergnes N., Brosselin P., Sanal O., Yegin O., Kutukculer N., Kilic S. S., Barlan I. B., Reisly I., Caracseghi F., Santos J. L., Llobet P., Carbone J., Granado L. I. G., Sanchez Ramon S., Tricas L., Matamoros N., Exley A., Kumaratne D., Alwood Z., Grimbacher B., Longhurst H., Knerr V., Bangs C., Boardman B., Tierney P., Chapel H., Notarangelo L. D., Plebani A., PIGNATA, CLAUDIO, Nickel R., Schauer U., Spath B., Caiser P., Roisler J., Bieneman K., Line R., Schubert R., El Helou S., Ritterbusch H., Goldacker S., Duckers G., Fabhauer M., Borte M., Notheis G., Belohradsky B. H., Sollinger F., Classen C. F., Apel K., Steinmann S., Muglich C., Szaflarska A., Bernatowska E., Heropolitansca E., Kuijpers T. W., van Beem R., Galal N. M., Reda S., Farber C. L., Meyts I., Velbri S., Kanariou M., Farmaki E., Papadopoulou Alataki E., Trachana M., Richter D., Blaziene A., Seidel M., Marques L., Feighery C., Cucuruz M., Konoplyannikova J., Paschenko O., Shcherbina A., Berglof A., Jardefors H., Wargstrom P., Brodszki N., Cantoni N., Dupenthaler A., Fahrni G., Hoernes M., Sahbacher U., Pasic S., Ciznar P., Jeverica A. K., Litzman J., Hlavackova E., Savchak I., Farkas H., Marodi L.
In order to build a common data pool and estimate the disease burden of primary immunodeficiencies (PID) in Europe, the European Society for Immunodeficiencies (ESID) has developed an internet-based database for clinical and research data on patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::fb433d2a6b74d41a4ba5638274f5db59
http://hdl.handle.net/11588/461322
http://hdl.handle.net/11588/461322