Профессор Paul Brogan

Omoyinmi, E., Standing, A., Keylock, A., Price-Kuehne, F., Melo-Gomes, S., Rowczenio, D., Nanthapisal, S., Cullup, T., Nyanhete, R., Ashton, E., Murphy, C., Clarke, M., Ahlfors, H., Jenkins, L., Gilmour, K., Eleftheriou, D., Lachmann, HJ., Hawkins, P.N., Klein, N., Brogan, P.A., 2017. Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis. PLoS One. 

Groot, N., Graeff, N., Avcin, T., Bader-Meunier, B., Brogan, P.A., Dolezalova, P., Feldman, B., Kone-Paut, I., Lahdenne, P., Marks S.D., McCann, L., Ozen, S., Pilkington, C., Ravelli, A., Royen-Kerkhof, A.V., Uziel, Y., Vastert, B., Wulffraat, N., Kamphuis, S., Beresford, M.W., 2017. European evidence-based recommendations for diagnosis and treatment of childhood-onset systemic lupus erythematosus: the SHARE initiative. 

Groot, N., Graeff, N., Avcin, T., Bader-Meunier, B., Dolezalova, P., Feldman, B., Kenet, G., Koné-Paut, I., Lahdenne, P., Marks, SD., McCann, L., Pilkington, CA., Ravelli, A., van, Royen-Kerkhof, A., Uziel, Y., Vastert, SJ., Wulffraat, N.M., Ozen, S., Brogan, P., Kamphuis, S., Beresford, M.W., 2017.  European evidence-based recommendations for diagnosis and treatment of paediatric antiphospholipid syndrome: the SHARE initiative. Ann Rheum Dis.

Nanthapisal, S., Omoyinmi, E., Murphy, C., Standing, A., Eisenhut, M., Eleftheriou, D., Brogan, P., 2017. Early-Onset Juvenile SLE Associated with a Novel Mutation in Protein.

Standing, A.S., Malinova, D., Hong, Y., Record, J., Moulding, D., Blundell, M.P., Nowak, K., Jones, H., Omoyinmi, E., Gilmour, K.C., Medlar, A., Stanescu, H., Kleta, R., Anderson, G., Nanthapisal, S., Gomes, S.M., Klein, N., Eleftheriou, D., Thrasher, A.J., Brogan, P.A., 2017. Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT).

Nanthapisal, S., Murphy, C., Omoyinmi, E., Hong, Y., Standing, A., Berg, S., Ekelund, M., Jolles, S., Harper, L., Youngstein, T., Gilmour, K., Klein, N.J., Eleftheriou, D., Brogan, P.A., 2017. Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen Cases. Arthritis Rheumatol. 68(9). Pp. 2314-22. 

Nanthapisal, S., Klein, N. J., Ambrose, N., Eleftheriou, D., Brogan, P.A., 2016. Paediatric Behçet's disease: a UK tertiary centre experience. Clin Rheumatol. 

Brehm, A., Liu, Y., Sheikh, A., Marrero, B., Omoyinmi,  E., Zhou, Q., Montealegre, G., Biancotto, A., Reinhardt, A., Almeida, de Jesus, A., Pelletier, M., Tsai, WL., Remmers, E.F., Kardava, L., Hill, S., Kim, H., Lachmann, H.J., Megarbane, A., Chae, JJ., Brady, J., Castillo, R.D., Brown, D., Casano, A.V., Gao, L, Chapelle, D., Huang, Y., Stone, D., Chen, Y., Sotzny, F., Lee C.C, Kastner, D.L., Torrelo, A., Zlotogorski, A., Moir, S., Gadina, M., McCoy, P., Wesley, R., Rother, K.I., Hildebrand, P.W., Brogan, P., Krüger, E., Aksentijevich, I., Goldbach-Mansky., 2015. Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS. J Clin Invest. 125(11). Pp. 4196-211. 

Shah, V., Christof, G., Mukasa, T., Brogan, K.S., Wade, A., Eleftheriou, D., Levin, M., Tulloh, R.M., Almeida, B., Dillon, M.J., Marek, J., Klein, N., Brogan, P.A., 2015. Cardiovascular status after Kawasaki disease in the UK. Heart. 10(20) pp. 1646-55. 

Eleftheriou, D., Varnier, G., Dolezalova, P., McMahon, A.M., Al-Obaidi, M., Brogan, P.A., 2015. Takayasu arteritis in childhood: retrospective experience from a tertiary referral centre in the United Kingdom. Arthritis Res Ther. 17(1) pp. 36.