The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry von Lachmann, H J, Papa, R, Gerhold, K, Obici, L, Touitou, I, Cantarini, L, Frenkel, J, Anton, J, Kone-Paut, I, Cattalini, M, Bader-Meunier, B, Insalaco, A, Hentgen, V, Merino, R, Modesto, C, Toplak, N, Berendes, R, Ozen, S, Cimaz, R, Jansson, A, Brogan, P A, Hawkins, P N, Ruperto, N, Martini, A, Woo, P, Gattorno, M

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Amyloid diseases of the heart: assessment, diagnosis, and referral von Dubrey, S W, Hawkins, P N, Falk, R H

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Two-year results from an open-label, multicentre, phase III study evaluating the safety and efficacy of canakinumab in patients with cryopyrin-associated periodic syndrome across d... von Kuemmerle-Deschner, Jasmin B, Hachulla, E, Cartwright, R, Hawkins, P N, Tran, T A, Bader-Meunier, B, Hoyer, J, Gattorno, M, Gul, A, Smith, J, Leslie, K S, Jiménez, S, Morell-Dubois, S, Davis, N, Patel, N, Widmer, A, Preiss, R, Lachmann, H J

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A matched comparison of cyclophosphamide, bortezomib and dexamethasone (CVD) versus risk-adapted cyclophosphamide, thalidomide and dexamethasone (CTD) in AL amyloidosis von Venner, C P, Gillmore, J D, Sachchithanantham, S, Mahmood, S, Lane, T, Foard, D, Rannigan, L, Gibbs, S D J, Pinney, J H, Whelan, C J, Lachmann, H J, Hawkins, P N, Wechalekar, A D

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Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosis von Pepys, M. B, Herbert, J, Hutchinson, W. L, Tennent, G. A, Lachmann, H. J, Gallimore, J. R, Lovat, L. B, Bartfai, T, Alanine, A, Hertel, C, Hoffmann, T, Jakob-Roetne, R, Norcross, R. D, Kemp, J. A, Yamamura, K, Suzuki, M, Taylor, G. W, Murray, S, Thompson, D, Purvis, A, Kolstoe, S, Wood, S. P, Hawkins, P. N

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Solid Organ Transplantation in AL Amyloidosis von Sattianayagam, P. T., Gibbs, S. D. J., Pinney, J. H., Wechalekar, A. D., Lachmann, H. J., Whelan, C. J., Gilbertson, J. A., Hawkins, P. N., Gillmore, J. D.

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Renal Transplantation in Systemic Amyloidosis—Importance of Amyloid Fibril Type and Precursor Protein Abundance von Pinney, J. H., Lachmann, H. J., Sattianayagam, P. T., Gibbs, S. D. J., Wechalekar, A. D., Venner, C. P., Whelan, C. J., Gilbertson, J. A., Rowczenio, D., Hawkins, P. N., Gillmore, J. D.

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Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations von Lachmann, H. J., Şengül, B., Yavuzşen, T. U., Booth, D. R., Booth, S. E., Bybee, A., Gallimore, J. R., Soytürk, M., Akar, S., Tunca, M., Hawkins, P. N.

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Hereditary lysozyme amyloidosis - phenotypic heterogeneity and the role of solid organ transplantation von Sattianayagam, P. T., Gibbs, S. D. J., Rowczenio, D., Pinney, J. H., Wechalekar, A. D., Gilbertson, J. A., Hawkins, P. N., Lachmann, H. J., Gillmore, J. D.

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Cardiac amyloidosis: where are we today? von Patel, K. S., Hawkins, P. N.

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T1 mapping and survival in systemic light-chain amyloidosis von Banypersad, Sanjay M, Fontana, Marianna, Maestrini, Viviana, Sado, Daniel M, Captur, Gabriella, Petrie, Aviva, Piechnik, Stefan K, Whelan, Carol J, Herrey, Anna S, Gillmore, Julian D, Lachmann, Helen J, Wechalekar, Ashutosh D, Hawkins, Philip N, Moon, James C

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Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis von Booth, David R, Sunde, Margaret, Bellotti, Vittorio, Robinson, Carol V, Hutchinson, Winston L, Fraser, Paul E, Hawkins, Philip N, Dobson, Christopher M, Radford, Sheena E, Blake, Colin C. F, Pepys, Mark B

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Muckle-Wells syndrome in an Indian family associated with NLRP3 mutation von Abdulla, M, Alungal, J, Hawkins, P, Mohammed, S

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Amyloidosis and the respiratory tract von Gillmore, Julian D, Hawkins, Philip N

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The genetic basis of autosomal dominant familial Mediterranean fever von Booth, D.R., Gillmore, J.D., Lachmann, H.J., Booth, S.E., Bybee, A., Soytürk, M., Akar, S., Pepys, M.B., Tunca, M., Hawkins, P.N.

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Progressive cardiac amyloidosis following liver transplantation for familial amyloid polyneuropathy : Implications for amyloid fibrillogenesis von STANGOU, A. J, HAWKINS, P. N, HEATON, N. D, RELA, M, MONAGHAN, M, NIHOYANNOPOULOS, P, O'GRADY, J, PEPYS, M. B, WILLIAMS, R

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Metabolic and scintigraphic studies of radioiodinated human C-reactive protein in health and disease von VIGUSHIN, D. M, PEPYS, M. B, HAWKINS, P. N

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Myocardial ischaemia in cardiac amyloidosis: a change of perspective von Ioannou, A, Chacko, L, Kotecha, T, Patel, R K, Razvi, Y, Porcari, A, Venneri, L, Martinez-Naharro, A, Knight, D, Brown, J, Hawkins, P N, Gillmore, J D, Fontana, M

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Bleeding symptoms and coagulation abnormalities in 337 patients with AL‐amyloidosis von Mumford, Andrew D., O'donnell, James, Gillmore, Julian D., Manning, Richard A., Hawkins, Philip N., Laffan, Michael

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A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK von Carr, A S, Pelayo-Negro, A L, Evans, M RB, Laurà, M, Blake, J, Stancanelli, C, Iodice, V, Wechalekar, A D, Whelan, C J, Gillmore, J D, Hawkins, P N, Reilly, M M

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