Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen Cases von Nanthapisal, Sira, Murphy, Claire, Omoyinmi, Ebun, Hong, Ying, Standing, Ariane, Berg, Stefan, Ekelund, Maria, Jolles, Stephen, Harper, Lorraine, Youngstein, Taryn, Gilmour, Kimberly, Klein, Nigel J., Eleftheriou, Despina, Brogan, Paul A.

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Recommendations for the management of autoinflammatory diseases von ter Haar, Nienke M, Oswald, Marlen, Jeyaratnam, Jerold, Anton, Jordi, Barron, Karyl S, Brogan, Paul A, Cantarini, Luca, Galeotti, Caroline, Grateau, Gilles, Hentgen, Veronique, Hofer, Michael, Kallinich, Tilmann, Kone-Paut, Isabelle, Lachmann, Helen J, Ozdogan, Huri, Ozen, Seza, Russo, Ricardo, Simon, Anna, Uziel, Yosef, Wouters, Carine, Feldman, Brian M, Vastert, Sebastiaan J, Wulffraat, Nico M, Benseler, Susanne M, Frenkel, Joost, Gattorno, Marco, Kuemmerle-Deschner, Jasmin B

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The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry von ter Haar, Nienke M., Jeyaratnam, Jerold, Lachmann, Helen J., Simon, Anna, Brogan, Paul A., Doglio, Matteo, Cattalini, Marco, Anton, Jordi, Modesto, Consuelo, Quartier, Pierre, Hoppenreijs, Esther, Martino, Silvana, Insalaco, Antonella, Cantarini, Luca, Lepore, Loredana, Alessio, Maria, Calvo Penades, Inmaculada, Boros, Christina, Consolini, Rita, Rigante, Donato, Russo, Ricardo, Pachlopnik Schmid, Jana, Lane, Thirusha, Martini, Alberto, Ruperto, Nicolino, Frenkel, Joost, Gattorno, Marco

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Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS disease von Dale, Russell C, Brilot, Fabienne, Duffy, Lisa V, Twilt, Marinka, Waldman, Amy T, Narula, Sona, Muscal, Eyal, Deiva, Kumaran, Andersen, Erik, Eyre, Michael R, Eleftheriou, Despina, Brogan, Paul A, Kneen, Rachel, Alper, Gulay, Anlar, Banu, Wassmer, Evangeline, Heineman, Kirsten, Hemingway, Cheryl, Riney, Catherine J, Kornberg, Andrew, Tardieu, Marc, Stocco, Amber, Banwell, Brenda, Gorman, Mark P, Benseler, Susanne M, Lim, Ming

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Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis von Omoyinmi, Ebun, Standing, Ariane, Keylock, Annette, Price-Kuehne, Fiona, Melo Gomes, Sonia, Rowczenio, Dorota, Nanthapisal, Sira, Cullup, Thomas, Nyanhete, Rodney, Ashton, Emma, Murphy, Claire, Clarke, Megan, Ahlfors, Helena, Jenkins, Lucy, Gilmour, Kimberly, Eleftheriou, Despina, Lachmann, Helen J, Hawkins, Philip N, Klein, Nigel, Brogan, Paul A

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Stimulator of Interferon Genes–Associated Vasculitis of Infancy von Omoyinmi, Ebun, Melo Gomes, Sonia, Nanthapisal, Sira, Woo, Patricia, Standing, Ariane, Eleftheriou, Despina, Klein, Nigel, Brogan, Paul A.

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Biologic therapy in refractory chronic non-bacterial osteomyelitis of childhood von Eleftheriou, Despina, Gerschman, Tommy, Sebire, Neil, Woo, Patricia, Pilkington, Clarissa A., Brogan, Paul A.

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Anti-Neutrophil Cytoplasmic Antibodies Stimulate Release of Neutrophil Microparticles von YING HONG, ELEFTHERIOU, Despina, HUSSAIN, Abdullah A. K, PRICE-KUEHNE, Fiona E, SAVAGE, Caroline O, JAYNE, David, LITTLE, Mark A, SALAMA, Alan D, KLEIN, Nigel J, BROGAN, Paul A

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Lentiviral Mediated ADA2 Gene Transfer Corrects the Defects Associated With Deficiency of Adenosine Deaminase Type 2 von Hong, Ying, Casimir, Marina, Houghton, Benjamin C, Zhang, Fang, Jensen, Barbara, Omoyinmi, Ebun, Torrance, Robert, Papadopoulou, Charalampia, Cummins, Michelle, Roderick, Marion, Thrasher, Adrian J, Brogan, Paul A, Eleftheriou, Despina

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Case Report: ISG15 deficiency caused by novel variants in two families and effective treatment with Janus kinase inhibition von Burleigh, Alice, Moraitis, Elena, Al Masroori, Eman, Al-Abadi, Eslam, Hong, Ying, Omoyinmi, Ebun, Titheradge, Hannah, Stals, Karen, Jones, Wendy D, Gait, Anthony, Jayarajan, Vignesh, Di, Wei-Li, Sebire, Neil, Solman, Lea, Ogboli, Malobi, Welch, Steven B, Sudarsanam, Annapurna, Wacogne, Ian, Price-Kuehne, Fiona, Jensen, Barbara, Brogan, Paul A, Eleftheriou, Despina

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Vasculitis in a patient with mevalonate kinase deficiency (MKD): a case report von Omoyinmi, Ebun, Rowczenio, Dorota, Sebire, Neil, Brogan, Paul A, Eleftheriou, Despina

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Neuroinflammation, autoinflammation, splenomegaly and anemia caused by bi-allelic mutations in IRAK4 von Cooray, Samantha, Price-Kuehne, Fiona, Hong, Ying, Omoyinmi, Ebun, Burleigh, Alice, Gilmour, Kimberly C., Ahmad, Bilal, Choi, Sangdun, Bahar, Mohammad W., Torpiano, Paul, Gagunashvili, Andrey, Jensen, Barbara, Bellos, Evangelos, Sancho-Shimizu, Vanessa, Herberg, Jethro A., Mankad, Kshitij, Kumar, Atul, Kaliakatsos, Marios, Worth, Austen J. J., Eleftheriou, Despina, Whittaker, Elizabeth, Brogan, Paul A.

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Cutaneous Vasculitis and Digital Ischaemia Caused by Heterozygous Gain-of-Function Mutation in C3 von Omoyinmi, Ebun, Mohamoud, Iman, Gilmour, Kimberly, Brogan, Paul A, Eleftheriou, Despina

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Janus kinase 1/2 inhibition with baricitinib in the treatment of juvenile dermatomyositis von Papadopoulou, Charalampia, Hong, Ying, Omoyinmi, Ebun, Brogan, Paul A, Eleftheriou, Despina

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Cutaneous Vasculitis and Recurrent Infection Caused by Deficiency in Complement Factor I von Nanthapisal, Sira, Eleftheriou, Despina, Gilmour, Kimberly, Leone, Valentina, Ramnath, Radhika, Omoyinmi, Ebun, Hong, Ying, Klein, Nigel, Brogan, Paul A

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Elicitation of expert prior opinion: application to the MYPAN trial in childhood polyarteritis nodosa von Hampson, Lisa V, Whitehead, John, Eleftheriou, Despina, Tudur-Smith, Catrin, Jones, Rachel, Jayne, David, Hickey, Helen, Beresford, Michael W, Bracaglia, Claudia, Caldas, Afonso, Cimaz, Rolando, Dehoorne, Joke, Dolezalova, Pavla, Friswell, Mark, Jelusic, Marija, Marks, Stephen D, Martin, Neil, McMahon, Anne-Marie, Peitz, Joachim, van Royen-Kerkhof, Annet, Soylemezoglu, Oguz, Brogan, Paul A

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Testicular ischemia in deficiency of adenosine deaminase 2 (DADA2) von Clarke, Katherine, Campbell, Cathy, Omoyinmi, Ebun, Hong, Ying, Al Obaidi, Muthana, Sebire, Neil, Brogan, Paul A

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Hereditary Systemic Autoinflammatory Diseases: Therapeutic Stratification von Kul Cinar, Ovgu, Putland, Amber, Wynne, Karen, Eleftheriou, Despina, Brogan, Paul A

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Biologic therapy in primary systemic vasculitis of the young von Eleftheriou, Despina, Melo, Marianna, Marks, Stephen D., Tullus, Kjell, Sills, John, Cleary, Gavin, Dolezalova, Pavla, Ozen, Seza, Pilkington, Clarissa, Woo, Pat, Klein, Nigel, Dillon, Michael J., Brogan, Paul A.

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A case of Myhre syndrome mimicking juvenile scleroderma von Jensen, Barbara, James, Rebecca, Hong, Ying, Omoyinmi, Ebun, Pilkington, Clarissa, Sebire, Neil J, Howell, Kevin J, Brogan, Paul A, Eleftheriou, Despina

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