Cyclosporine A for severe atopic dermatitis in children. efficacy and safety in a retrospective study of 63 patients von Hernández‐Martín, A., Noguera‐Morel, L., Bernardino‐Cuesta, B., Torrelo, A., Pérez‐Martin, M.A., Aparicio‐López, C., Lucas‐Collantes, C.

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Burosumab for X-linked hypophosphatemia in children and adolescents: Opinion based on early experience in seven European countries von Mughal, M Zulf, Baroncelli, Giampiero I, de Lucas-Collantes, Carmen, Linglart, Agnès, Magnolato, Andrea, Raimann, Adalbert, Santos, Fernando, Schnabel, Dirk, Shaw, Nick, Nilsson, Ola

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Post-authorisation safety study of burosumab use in paediatric, adolescent and adult patients with X-linked hypophosphataemia: rationale and description von Brandi, Maria Luisa, Ariceta, Gema, Beck-Nielsen, Signe Sparre, Boot, Annemieke M., Briot, Karine, de Lucas Collantes, Carmen, Emma, Francesco, Giannini, Sandro, Haffner, Dieter, Keen, Richard, Levtchenko, Elena, Mӓkitie, Outi, Nilsson, Ola, Schnabel, Dirk, Tripto-Shkolnik, Liana, Zillikens, M. Carola, Liu, Jonathan, Tudor, Alina, Mughal, M. Zulf

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Tuberous sclerosis complex: analysis of areas of involvement, treatment progress and translation to routine clinical practice in a cohort of paediatric patients von Cantarín-Extremera, V, Bernardino-Cuesta, B, Martín-Villaescusa, C, Melero-Llorente, J, Hernández-Martín, A, Aparicio-López, C, de Lucas-Collantes, C, Tamariz Martel-Moreno, A, Duat-Rodríguez, A, Ruiz-Falcó-Rojas, M L

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DECTIN-1: A modifier protein in CTLA-4 haploinsufficiency von Turnbull, Cynthia, Bones, Josiah, Stanley, Maurice, Medhavy, Arti, Wang, Hao, Lorenzo, Ayla May D, Cappello, Jean, Shanmuganandam, Somasundhari, Pandey, Abhimanu, Seneviratne, Sandali, Brown, Grant J, Meng, Xiangpeng, Fulcher, David, Burgio, Gaetan, Man, Si Ming, de Lucas Collantes, Carmen, Gasior, Mercedes, López Granados, Eduardo, Martin, Pilar, Jiang, Simon H, Cook, Matthew C, Ellyard, Julia I, Athanasopoulos, Vicki, Corry, Ben, Canete, Pablo F, Vinuesa, Carola G

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Minimal Change Disease Is Associated With Endothelial Glycocalyx Degradation and Endothelial Activation von Bauer, Colin, Piani, Federica, Banks, Mindy, Ordoñez, Flor A., de Lucas-Collantes, Carmen, Oshima, Kaori, Schmidt, Eric P., Zakharevich, Igor, Segarra, Alfons, Martinez, Cristina, Roncal-Jimenez, Carlos, Satchell, Simon C., Bjornstad, Petter, Lucia, Marshall Scott, Blaine, Judith, Thurman, Joshua M., Johnson, Richard J., Cara-Fuentes, Gabriel

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TLR7 gain-of-function genetic variation causes human lupus von Brown, Grant J., Cañete, Pablo F., Wang, Hao, Medhavy, Arti, Bones, Josiah, Roco, Jonathan A., He, Yuke, Qin, Yuting, Cappello, Jean, Ellyard, Julia I., Bassett, Katharine, Shen, Qian, Burgio, Gaetan, Zhang, Yaoyuan, Turnbull, Cynthia, Meng, Xiangpeng, Wu, Phil, Cho, Eun, Miosge, Lisa A., Andrews, T. Daniel, Field, Matt A., Tvorogov, Denis, Lopez, Angel F., Babon, Jeffrey J., López, Cristina Aparicio, Gónzalez-Murillo, África, Garulo, Daniel Clemente, Pascual, Virginia, Levy, Tess, Mallack, Eric J., Calame, Daniel G., Lotze, Timothy, Lupski, James R., Ding, Huihua, Ullah, Tomalika R., Walters, Giles D., Koina, Mark E., Cook, Matthew C., Shen, Nan, de Lucas Collantes, Carmen, Corry, Ben, Gantier, Michael P., Athanasopoulos, Vicki, Vinuesa, Carola G.

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Functional rare and low frequency variants in BLK and BANK1 contribute to human lupus von Jiang, Simon H., Athanasopoulos, Vicki, Ellyard, Julia I., Chuah, Aaron, Cappello, Jean, Cook, Amelia, Prabhu, Savit B., Cardenas, Jacob, Gu, Jinghua, Stanley, Maurice, Roco, Jonathan A., Papa, Ilenia, Yabas, Mehmet, Walters, Giles D., Burgio, Gaetan, McKeon, Kathryn, Byers, James M., Burrin, Charlotte, Enders, Anselm, Miosge, Lisa A., Canete, Pablo F., Jelusic, Marija, Tasic, Velibor, Lungu, Adrian C., Alexander, Stephen I., Kitching, Arthur R., Fulcher, David A., Shen, Nan, Arsov, Todor, Gatenby, Paul A., Babon, Jeff J., Mallon, Dominic F., de Lucas Collantes, Carmen, Stone, Eric A., Wu, Philip, Field, Matthew A., Andrews, Thomas D., Cho, Eun, Pascual, Virginia, Cook, Matthew C., Vinuesa, Carola G.

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