Familial haemophagocytic lymphohistiocytosis: advances in the genetic basis, diagnosis and management by Gholam, C., Grigoriadou, S., Gilmour, K. C., Gaspar, H. B.

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British Society for Immunology and United Kingdom Primary Immunodeficiency Network (UKPIN) consensus guideline for the management of immunoglobulin replacement therapy by Grigoriadou, S, Clubbe, R, Garcez, T, Huissoon, A, Grosse-Kreul, D, Jolles, S, Henderson, K, Edmonds, J, Lowe, D, Bethune, C

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Hypogammaglobulinaemia after rituximab treatment-incidence and outcomes by Makatsori, M, Kiani-Alikhan, S, Manson, A L, Verma, N, Leandro, M, Gurugama, N P, Longhurst, H J, Grigoriadou, S, Buckland, M, Kanfer, E, Hanson, S, Ibrahim, M A A, Grimbacher, B, Chee, R, Seneviratne, S L

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A UK national audit of hereditary and acquired angioedema by Jolles, S., Williams, P., Carne, E., Mian, H., Huissoon, A., Wong, G., Hackett, S., Lortan, J., Platts, V., Longhurst, H., Grigoriadou, S., Dempster, J., Deacock, S., Khan, S., Darroch, J., Simon, C., Thomas, M., Pavaladurai, V., Alachkar, H., Herwadkar, A., Abinun, M., Arkwright, P., Tarzi, M., Helbert, M., Bangs, C., Pastacaldi, C., Phillips, C., Bennett, H., El‐Shanawany, T.

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British Society for Immunology/United Kingdom Primary Immunodeficiency Network consensus statement on managing non‐infectious complications of common variable immunodeficiency diso... by Bethune, C., Egner, W., Garcez, T., Huissoon, A., Jolles, S., Karim, Y., Jain, R., Savic, S., Kelley, K., Grosse‐Kreul, D., Grigoriadou, S.

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Immune deficiency: changing spectrum of pathogens by Duraisingham, S. S., Manson, A., Grigoriadou, S., Buckland, M., Tong, C. Y. W., Longhurst, H. J.

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The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years' activity 2008–2012 by Edgar, J. D. M., Buckland, M., Guzman, D., Conlon, N. P., Knerr, V., Bangs, C., Reiser, V., Panahloo, Z., Workman, S., Slatter, M., Gennery, A. R., Davies, E. G., Allwood, Z., Arkwright, P. D., Helbert, M., Longhurst, H. J., Grigoriadou, S., Devlin, L. A., Huissoon, A., Krishna, M. T., Hackett, S., Kumararatne, D. S., Condliffe, A. M., Baxendale, H., Henderson, K., Bethune, C., Symons, C., Wood, P., Ford, K., Patel, S., Jain, R., Jolles, S., El‐Shanawany, T., Alachkar, H., Herwadkar, A., Sargur, R., Shrimpton, A., Hayman, G., Abuzakouk, M., Spickett, G., Darroch, C. J., Paulus, S., Marshall, S. E., McDermott, E. M., Heath, P. T., Herriot, R., Noorani, S., Turner, M., Khan, S., Grimbacher, B.

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Clinical Immunology Review Series: An approach to the patient with angio-oedema by Grigoriadou, S, Longhurst, H.J

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Clinical Immunology Review Series: An approach to the management of pulmonary disease in primary antibody deficiency by Tarzi, M.D, Grigoriadou, S, Carr, S.B, Kuitert, L.M, Longhurst, H.J

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In pursuit of excellence: an integrated care pathway for C1 inhibitor deficiency by Manson, A. L., Price, A., Dempster, J., Clinton‐Tarestad, P., Greening, C., Enti, R., Hill, S., Grigoriadou, S., Buckland, M. S., Longhurst, H. J.

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Changes in B cell immunophenotype in common variable immunodeficiency: cause or effect – is bronchiectasis indicative of undiagnosed immunodeficiency? by Bright, P., Grigoriadou, S., Kamperidis, P., Buckland, M., Hickey, A., Longhurst, H. J.

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Mullins' syndrome: a new gammopathy-related autoinflammatory syndrome resistant to anakinra by Longhurst, H J, Yong, P F K, Manson, A L, Cavenagh, J D, Grigoriadou, S, Buckland, M S

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Is Screening with C4 Complement Level Enough to Exclude Hereditary Angioedema? by Grigoriadou, S., Duddridge, M.

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COVID-19 in patients with primary and secondary immunodeficiency: The United Kingdom experience by Shields, Adrian M., Burns, Siobhan O., Savic, Sinisa, Richter, Alex G., Anantharachagan, Ariharan, Arumugakani, Gururaj, Baker, Kenneth, Bahal, Sameer, Bermingham, William, Bhole, Malini, Boules, Evon, Bright, Philip, Burns, Siobhan, Cleave, Betsy, Dempster, John, Devlin, Lisa, Dhalla, Fatima, Drewe, Elizabeth, Duncan, Christopher, Dziadzio, Magdalena, Elkhalifa, Shuayb, Gennery, Andrew, Goddard, Sarah, Grigoriadou, Sofia, Hayman, Grant, Herwadkar, Archana, Huissoon, Aarnoud, Jain, Rashmi, Jolles, Stephen, Johnston, Sarah, Leeman, Lucy, Mahabir, Shanti, MacLochlainn, Dylan, McDermott, Elizabeth, Misbah, Siraj, Morsi, Hadeil, Murng, Sai, Noorani, Sadia, O’Brien, Rachael, Patel, Smita, Price, Arthur, Richter, Alex, Savic, Sinisa, Seneviratne, Suranjith, Shields, Adrian, Shrimpton, Anna, Stroud, Catherine, Vaitla, Prashantha, Verma, Nisha

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Blocking T cell co-stimulation in primary Sjögren's syndrome: rationale, clinical efficacy and modulation of peripheral and salivary gland biomarkers by Pontarini, Elena, Verstappen, Gwenny M, Grigoriadou, Sofia, Kroese, Frans G M, Bootsma, Hendrika, Bombardieri, Michele

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B cell depletion with rituximab in the treatment of primary Sjögren's syndrome: what have we learnt? by Grigoriadou, Sofia, Chowdhury, Farzana, Pontarini, Elena, Tappuni, Anwar, Bowman, Simon J, Bombardieri, Michele

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Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity by Wolkewitz, Martin, Schwab, Charlotte, Lorenzini, Tiziana, Leiding, Jennifer W., Aladjdi, Nathalie, Abou-Chahla, Wadih, Baris, Safa, Barlogis, Vincent, Barzaghi, Federica, Baumann, Ulrich, Bloomfield, Marketa, Bohynikova, Nadezda, Bodet, Damien, Burns, Siobhan O., Cathébras, Pascal, Ekwall, Olov, Frange, Pierre, Geier, Christoph, Goda, Vera, Hammarström, Lennart, Hauck, Fabian, Heropolitanska-Pliszka, Edyta, Jolles, Stephen, Karakoc-Aydiner, Elif, Kindle, Gerhard R., Klemann, Christian, Koltan, Sylwia, Krüger, Renate, Jeziorski, Eric, Lougaris, Vassilios, Marzollo, Antonio, Mahlaoui, Nizar, Malphettes, Marion, Meinhardt, Andrea, Merlin, Etienne, Meyts, Isabelle, Milota, Tomas, Moshous, Despina, Mukhina, Anna, Neven, Benedicte, Nieters, Alexandra, Nove-Josserand, Raphaele, Oksenhendler, Eric, Ozen, Ahmet, Olbrich, Peter, Pac, Malgorzata, Parra-Martinez, Alba, Paschenko, Olga, Prader, Seraina, Raffray, Loic, Ritterbusch, Henrike, Riviere, Jacques G., Rusch, Stephan, Sakovich, Inga, Savic, Sinisa, Schuetz, Catharina, Schulz, Ansgar, Sediva, Anna, Semeraro, Michaela, Slatter, Mary A., Stephan, Jean-Louis, Suarez, Felipe, Trück, Johannes, van Aerde, Koen J., von Bernuth, Horst, Warnatz, Klaus, Ip, Winnie, Picard, Capucine, Grimbacher, Bodo, Kracker, Sven, Condliffe, Alison M., Ehl, Stephan, Gennery, Andrew, Tantou, Sofia, Grigoriadou, Sofia, Cericola, Gabriella, Scheibenbogen, Carmen, Krivan, Gergely, McGuire, Frances K., Leahy, Timothy Ronan, Edgar, John David M., Bakhtiar, Shahrzad, Bader, Peter, Rohner, Geraldine Blanchard, Haerynck, Filomeen, Claes, Karlien, Fasshauer, Maria, Graf, Dagmar, Jeseňák, Miloš, Fabio, Giovanna, Giardino, Giuliana, Karadağ, Ilknur Kökçü, Yıldıran, Alişan, Steinmann, Sandra, Pietrucha, Barbara Maria, Gernert, Michael, Witte, Torsten, Wolska-Kusnierz, Beata, Zabara, Dariia V., Shvets, Oksana A.

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Hypogammaglobulinaemia after rituximab treatment--incidence and outcomes by Makatsori, M., Kiani-Alikhan, S., Manson, A. L., Verma, N., Leandro, M., Gurugama, N. P., Longhurst, H. J., Grigoriadou, S., Buckland, M., Kanfer, E., Hanson, S., Ibrahim, M. A. A., Grimbacher, B., Chee, R., Seneviratne, S. L.

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The Icatibant Outcome Survey: experience of hereditary angioedema management from six European countries by 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.

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Solvable cases of Szebehely's equation by Grigoriadou, S, Bozis, G, Elmabsout, B

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