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Walnut Allergy Across Europe: Distribution of Allergen Sensitization Patterns and Prediction of Severity

Autor: Lyons, S.A. Datema, M.R. Le, T.-M. Asero, R. Barreales, L. Belohlavkova, S. de Blay, F. Clausen, M. Dubakiene, R. Fernández-Perez, C. Fritsche, P. Gislason, D. Hoffmann-Sommergruber, K. Jedrzejczak-Czechowicz, M. Jongejan, L. Kowalski, M.L. Kralimarkova, T.Z. Lidholm, J. Papadopoulos, N.G. Pontoppidan, B. Popov, T.A. Prado, N.D. Purohit, A. Reig, I. Seneviratne, S.L. Sinaniotis, A. Vassilopoulou, E. Versteeg, S.A. Vieths, S. Zwinderman, A.H. Welsing, P.M.J. Mills, E.N.C. Ballmer-Weber, B.K. Knulst, A.C. Fernández-Rivas, M. Van Ree, R.

Background: Walnut allergy is common across the globe, but data on the involvement of individual walnut components are scarce. Objectives: To identify geographical differences in walnut component sensitization across Europe, explore cosensitization a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::0bdd8d2261ff3e86b3de702d9ce0d8cf
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3103316

Pathogenesis of liver involvement during dengue viral infections

Autor: Seneviratne, S.L., Malavige, G.N., de Silva, H.J.

Publikováno v: In Transactions of the Royal Society of Tropical Medicine and Hygiene 2006 100(7):608-614

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Autor: Tuijnenburg, P., Lango Allen, H., Burns, S.O., Greene, D., Jansen, M.H., Staples, E., Stephens, J., Carss, K.J., Biasci, D., Baxendale, H., Thomas, M., Chandra, A., Kiani-Alikhan, S., Longhurst, H.J., Seneviratne, S.L., Oksenhendler, E., Simeoni, I., de Bree, G.J., Tool, A.T.J., van Leeuwen, E.M.M., Ebberink, E.H.T.M., Meijer, A.B., Tuna, S., Whitehorn, D., Brown, M., Turro, E., Thrasher, A.J., Smith, K.G.C., Thaventhiran, J.E., Kuijpers, T.W., Adhya, Z., Alachkar, H., Anantharachagan, A., Antrobus, R., Arumugakani, G., Bacchelli, C., Bethune, C., Bibi, S., Boardman, B., Booth, C., Browning, M., Brownlie, M., Burns, S., Clifford, H., Cooper, N., Davies, S., Dempster, J., Devlin, L., Doffinger, R., Drewe, E., Edgar, D., Egner, W., El-Shanawany, T., Gaspar, B., Ghurye, R., Gilmour, K., Goddard, S., Gordins, P., Grigoriadou, S., Hackett, S., Hague, R., Harper, L., Hayman, G., Herwadkar, A., Hughes, S., Huissoon, A., Jolles, S., Jones, J., Kelleher, P., Klein, N., Kuijpers, T., Kumararatne, D., Laffan, J., Allen, H.L., Lear, S., Longhurst, H., Lorenzo, L., Maimaris, J., Manson, A., McDermott, E., Millar, H., Mistry, A., Morrisson, V., Murng, S., Nasir, I., Nejentsev, S.

Background: The genetic cause of primary immunodeficiency disease (PID) carries prognostic information. Objective: We conducted a whole-genome sequencing study assessing a large proportion of the NIHR BioResource–Rare Diseases cohort. Methods: In t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::e5136ff0d169ccaaba0690640b9a494d
https://eprints.whiterose.ac.uk/132993/1/1-s2.0-S0091674918302860-main.pdf

British Lung Foundation/United Kingdom Primary Immunodeficiency Network Consensus Statement on the Definition, Diagnosis, and Management of Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders\ud

Autor: Hurst, J.R., Verma, N., Lowe, D., Baxendale, H.E., Jolles, S., Kelleher, P., Longhurst, H.J., Patel, S.Y., Renzoni, E.A., Sander, C.R., Avery, G.R., Babar, J.L., Buckland, M.S., Burns, S., Egner, W., Gompels, M.M., Gordins, P., Haddock, J.A., Hart, S.P., Hayman, G.R., Herriot, R., Hoyles, R.K., Huissoon, A.P., Jacob, J., Nicholson, A.G., Rassl, D.M., Sargur, R.B., Savic, S., Seneviratne, S.L., Sheaff, M., Vaitla, P.M., Walters, G.I., Whitehouse, J.L., Wright, P.A., Condliffe, A.M.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::0d4d352b3aa73a15fb7a9db7284b49fc
https://eprints.whiterose.ac.uk/111211/10/1-s2.0-S2213219817300351-main.pdf