A combined CFD modeling and experimental study of pyrolytic carbon deposition von Yu, Kehan, Hayman, Clifford C., Manjunath, S., Fan, Wei, Martin, Ina T., Martin, Heidi B., Sankaran, R. Mohan

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DIAMOND APPARATUS AND METHOD OF MANUFACTURE von HESS, ALLISON, ZORMAN, CHRISTIAN, SABANS, DAVID, HALPERN, JEFFREY, M, HAYMAN, CLIFFORD, C, MARTIN, HEIDI, B

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DIAMOND APPARATUS AND METHOD OF MANUFACTURE von SABENS DAVID M, HALPERN JEFFREY M, HAYMAN CLIFFORD C, MARTIN HEIDI B, HESS ALLISON E, ZORMAN CHRISTAIN A

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METHOD FOR ENCAPSULATING WATER-INSOLUBLE PARTICLES von HAYMAN, CLIFFORD C

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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations von Lorenzini, Tiziana, Fliegauf, Manfred, Klammer, Nils, Proietti, Michele, Bulashevska, Alla, Schejter, Yael D., Atschekzei, Faranaz, Stepensky, Polina, Pedroza, Luis A., van der Flier, Michiel, Martínez-Gallo, Mónica, Svec, Peter, Fischer, Ute, Ip, Winnie, Geha, Raif, Chou, Janet, Alosaimi, Mohammed, Weintraub, Lauren, Dos Santos Vilela, Maria Marluce, Holzinger, Dirk, Seidl, Maximilian, Lougaris, Vassilios, Plebani, Alessandro, Abolhassani, Hassan, Thaventhiran, James E., Warnatz, Klaus, Grimbacher, Bodo, Ashford, Sofie, Bacchelli, Chiara, Batista, Joana, Bibi, Shahnaz, Boardman, Barbara, Booth, Claire, Breen, Gerome, Burns, Siobhan O., Burren, Oliver S., Carss, Keren, Chambers, John, Cooper, Nichola, Davies, E.G., Dempster, John, Dewhurst, Eleanor F., Drewe, Elizabeth, Duarte, Daniel, Edgar, J. David M., Egner, William, El-Shanawany, Tariq, Erwood, Marie, Fox, James, Frontini, Mattia, Furnell, Abigail, Gaspar, H. Bobby, Gleadall, Nicholas S., Grigoriadou, Sofia, Hackett, Scott, Hague, Rosie, Haimel, Matthias, Hayman, Grant, Hu, Fengyuan, Huissoon, Aarnoud P., Jolles, Stephen, Kasanicki, Mary A., Kelleher, Peter, Klein, Nigel, Kreuzhuber, Roman, Kuijpers, Taco W., Kumararatne, Dinakantha, Allen, Hana Lango, Linger, Rachel, Lorenzo, Lorena E., Maimaris, Jesmeen, Martin, Jennifer, McDermott, Elizabeth M., Meacham, Stuart, Morrisson, Valerie, Nasir, Iman, Nejentsev, Sergey, Papadia, Sofia, Ponsford, Mark J., Quinn, Ellen, Quinti, Isabella, Rayner-Matthews, Paula J., Samani, Nilesh, Sanchis-Juan, Alba, Savic, Sinisa, Simpson, Michael A., Smith, Kenneth G.C., Thaventhiran, James E., Tilly, Tobias, Titterton, Catherine, Tuna, Salih, Urniaz, Rafal, von Ziegenweidt, Julie, Watt, Christopher, Welch, Steven B., Whitehorn, Deborah, Wood, Yvette, Workman, Sarita, Worth, Austen, Young, Timothy

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Improved quality of life after bilateral laparoscopic adrenalectomy for cushing's disease : A 10-year experience von THOMPSON, Sarah K, HAYMAN, Amanda V, LUDLAM, William H, DEVENEY, Clifford W, LORIAUX, D. Lynn, SHEPPARD, Brett C

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Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma von Minskaia, Ekaterina, Maimaris, Jesmeen, Jenkins, Persephone, Albuquerque, Adriana S., Hong, Ying, Eleftheriou, Despina, Gilmour, Kimberly C., Grace, Richard, Moreira, Fernando, Grimbacher, Bodo, Morris, Emma C., Burns, Siobhan O.

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Practical challenges for functional validation of STAT1 gain of function genetic variants von Albuquerque, Adriana S, Maimaris, Jesmeen, McKenna, Alexander J, Lambourne, Jonathan, Moreira, Fernando, Workman, Sarita, Megy, Karyn, Simeoni, Ilenia, Lango Allen, Hana, Morris, Emma C, Burns, Siobhan O

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Loss‐of‐function mutations in CSF3R cause moderate neutropenia with fully mature neutrophils: two novel pedigrees von Sprenkeler, Evelien G. G., Tool, Anton T. J., Kreft, Iris C., Alphen, Floris P. J., Seneviratne, Suranjith L., Maimaris, Jesmeen, Luqmani, Asad, Leeuwen, Karin, Bruggen, Robin, Burns, Siobhan O., Kuijpers, Taco W.

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Improved Quality of Life After Bilateral Laparoscopic Adrenalectomy for Cushing's Disease von Thompson, Sarah K., Hayman, Amanda V., Ludlam, William H., Deveney, Clifford W., Loriaux, D Lynn, Sheppard, Brett C.

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North American Male Reference Population for Speed of Sound in Bone at Multiple Skeletal Sites von Hayman, Stephen R., Drake, William M., Kendler, David L., Olszynski, Wojciech P., Webber, Colin E., Rosen, Clifford J., Genant, Harry K., Orwoll, Eric S., Pickard, Laura E., Adachi, Jonathan D.

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

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