Comedy for animators

por Lyons, Jonathan
Publicado 2016

Primary atopic disorders

por Lyons, Jonathan J., Milner, Joshua D.
Publicado 2018

Glycans Instructing Immunity: The Emerging Role of Altered Glycosylation in Clinical Immunology

por Lyons, Jonathan J., Milner, Joshua D., Rosenzweig, Sergio D.
Publicado 2015

Low hydroxychloroquine blood levels in patients who have had gastric bypass surgery

por Thomas, Donald E, Lyons, Jonathan S, Greene, Barry S, Petri, Michelle A
Publicado 2019

ISCEV guidelines for clinical multifocal electroretinography (2007 edition)

por Hood, Donald C., Bach, Michael, Brigell, Mitchell, Keating, David, Kondo, Mineo, Lyons, Jonathan S., Palmowski-Wolfe, Anja M.
Publicado 2007

Impact of naturally forming human α/β-tryptase heterotetramers in the pathogenesis of hereditary α-tryptasemia

por Le, Quang T., Lyons, Jonathan J., Naranjo, Andrea N., Olivera, Ana, Lazarus, Robert A., Metcalfe, Dean D., Milner, Joshua D., Schwartz, Lawrence B.
Publicado 2019

Challenges in applying diagnostic criteria for systemic mastocytosis

por Boggs, Nathan A., Sun, Xiaoping, Lyons, Jonathan J., McMurray, Jeremy C., Rose, David M., Pryor, Eric M., Metcalfe, Dean D., Maric, Irina
Publicado 2023

Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders

por Vazquez, Maribel, Chovanec, Jack, Kim, Jiwon, DiMaggio, Thomas, Milner, Joshua D., Francomano, Clair A., Gurnett, Christina A., Ritelli, Marco, Colombi, Marina, Lyons, Jonathan J.
Publicado 2022

Clinical Impact of Inherited and Acquired Genetic Variants in Mastocytosis

por Nedoszytko, Boguslaw, Arock, Michel, Lyons, Jonathan J., Bachelot, Guillaume, Schwartz, Lawrence B., Reiter, Andreas, Jawhar, Mohamad, Schwaab, Juliana, Lange, Magdalena, Greiner, Georg, Hoermann, Gregor, Niedoszytko, Marek, Metcalfe, Dean D., Valent, Peter
Publicado 2021

PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients

por Zhang, Yuan, Ma, Chi A., Lawrence, Monica G., Break, Timothy J., O’Connell, Michael P., Lyons, Jonathan J., López, Diego B., Barber, John S., Zhao, Yongge, Barber, Daniel L., Freeman, Alexandra F., Holland, Steven M., Lionakis, Michail S., Milner, Joshua D.
Publicado 2017

Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity

por Beers, Breanna J., Similuk, Morgan N., Ghosh, Rajarshi, Seifert, Bryce A., Jamal, Leila, Kamen, Michael, Setzer, Michael R., Jodarski, Colleen, Duncan, Rylee, Hunt, Devin, Mixer, Madison, Cao, Wenjia, Bi, Weimin, Veltri, Daniel, Karlins, Eric, Zhang, Lingwen, Li, Zhiwen, Oler, Andrew J., Jevtich, Kathleen, Yu, Yunting, Hullfish, Haley, Bielekova, Bibiana, Frischmeyer-Guerrerio, Pamela, Dang Do, An, Huryn, Laryssa A., Olivier, Kenneth N., Su, Helen C., Lyons, Jonathan J., Zerbe, Christa S., Rao, V. Koneti, Keller, Michael D., Freeman, Alexandra F., Holland, Steven M., Franco, Luis M., Walkiewicz, Magdalena A., Yan, Jia
Publicado 2023

Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early onset autoinflammatory syndrome

por Zhou, Qing, Wang, Hongying, Schwartz, Daniella M., Stoffels, Monique, Park, Yong Hwan, Zhang, Yuan, Yang, Dan, Demirkaya, Erkan, Takeuchi, Masaki, Tsai, Wanxia Li, Lyons, Jonathan J., Yu, Xiaomin, Ouyang, Claudia, Chen, Celeste, Chin, David T., Zaal, Kristien, Chandrasekharappa, Settara C., Hanson, Eric P., Yu, Zhen, Mullikin, James C., Hasni, Sarfaraz A., Wertz, Ingrid, Ombrello, Amanda K., Stone, Deborah L., Hoffmann, Patrycja, Jones, Anne, Barham, Beverly K., Leavis, Helen L., van Royen-Kerkof, Annet, Sibley, Cailin, Batu, Ezgi D., Gül, Ahmet, Siegel, Richard M., Boehm, Manfred, Milner, Joshua D., Ozen, Seza, Gadina, Massimo, Chae, JaeJin, Laxer, Ronald M., Kastner, Daniel L., Aksentijevich, Ivona
Publicado 2015

Germline hypomorphic CARD11 mutations in severe atopic disease

por Ma, Chi A, Stinson, Jeffrey R, Zhang, Yuan, Abbott, Jordan K, Weinreich, Michael A, Hauk, Pia J, Reynolds, Paul R, Lyons, Jonathan J, Nelson, Celeste G, Ruffo, Elisa, Dorjbal, Batsukh, Glauzy, Salomé, Yamakawa, Natsuko, Arjunaraja, Swadhinya, Voss, Kelsey, Stoddard, Jennifer, Niemela, Julie, Zhang, Yu, Rosenzweig, Sergio D, McElwee, Joshua J, DiMaggio, Thomas, Matthews, Helen F, Jones, Nina, Stone, Kelly D, Palma, Alejandro, Oleastro, Matías, Prieto, Emma, Bernasconi, Andrea R, Dubra, Geronimo, Danielian, Silvia, Zaiat, Jonathan, Marti, Marcelo A, Kim, Brian, Cooper, Megan A, Romberg, Neil D, Meffre, Eric, Gelfand, Erwin W, Snow, Andrew L, Milner, Joshua D
Publicado 2017

Updated Diagnostic Criteria and Classification of Mast Cell Disorders: A Consensus Proposal

por Valent, Peter, Akin, Cem, Hartmann, Karin, Alvarez-Twose, Ivan, Brockow, Knut, Hermine, Olivier, Niedoszytko, Marek, Schwaab, Juliana, Lyons, Jonathan J., Carter, Melody C., Elberink, Hanneke Oude, Butterfield, Joseph H., George, Tracy I., Greiner, Georg, Ustun, Celalettin, Bonadonna, Patrizia, Sotlar, Karl, Nilsson, Gunnar, Jawhar, Mohamad, Siebenhaar, Frank, Broesby-Olsen, Sigurd, Yavuz, Selim, Zanotti, Roberta, Lange, Magdalena, Nedoszytko, Boguslaw, Hoermann, Gregor, Castells, Mariana, Radia, Deepti H., Muñoz-Gonzalez, Javier I., Sperr, Wolfgang R., Triggiani, Massimo, Kluin-Nelemans, Hanneke C., Galli, Stephen J., Schwartz, Lawrence B., Reiter, Andreas, Orfao, Alberto, Gotlib, Jason, Arock, Michel, Horny, Hans-Peter, Metcalfe, Dean D.
Publicado 2021

Genetically defined individual reference ranges for tryptase limit unnecessary procedures and unmask myeloid neoplasms

por Chovanec, Jack, Tunc, Ilker, Hughes, Jason, Halstead, Joseph, Mateja, Allyson, Liu, Yihui, O’Connell, Michael P., Kim, Jiwon, Park, Young Hwan, Wang, Qinlu, Le, Quang, Pirooznia, Mehdi, Trivedi, Neil N., Bai, Yun, Yin, Yuzhi, Hsu, Amy P., McElwee, Joshua, Lassiter, Sheryce, Nelson, Celeste, Bandoh, Judy, DiMaggio, Thomas, Šelb, Julij, Rijavec, Matija, Carter, Melody C., Komarow, Hirsh D., Sabato, Vito, Steinberg, Joshua, Hafer, Kurt M., Feuille, Elizabeth, Hourigan, Christopher S., Lack, Justin, Khoury, Paneez, Maric, Irina, Zanotti, Roberta, Bonadonna, Patrizia, Schwartz, Lawrence B., Milner, Joshua D., Glover, Sarah C., Ebo, Didier G., Korošec, Peter, Caughey, George H., Brittain, Erica H., Busby, Ben, Metcalfe, Dean D., Lyons, Jonathan J.
Publicado 2022

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

por Sharma, Mehul, Leung, Daniel, Momenilandi, Mana, Jones, Lauren C.W., Pacillo, Lucia, James, Alyssa E., Murrell, Jill R., Delafontaine, Selket, Maimaris, Jesmeen, Vaseghi-Shanjani, Maryam, Del Bel, Kate L., Lu, Henry Y., Chua, Gilbert T., Di Cesare, Silvia, Fornes, Oriol, Liu, Zhongyi, Di Matteo, Gigliola, Fu, Maggie P., Amodio, Donato, Tam, Issan Yee San, Chan, Gavin Shueng Wai, Sharma, Ashish A., Dalmann, Joshua, van der Lee, Robin, Blanchard-Rohner, Géraldine, Lin, Susan, Philippot, Quentin, Richmond, Phillip A., Lee, Jessica J., Matthews, Allison, Seear, Michael, Turvey, Alexandra K., Philips, Rachael L., Brown-Whitehorn, Terri F., Gray, Christopher J., Izumi, Kosuke, Treat, James R., Wood, Kathleen H., Lack, Justin, Khleborodova, Asya, Niemela, Julie E., Yang, Xingtian, Liang, Rui, Kui, Lin, Wong, Christina Sze Man, Poon, Grace Wing Kit, Hoischen, Alexander, van der Made, Caspar I., Yang, Jing, Chan, Koon Wing, Rosa Duque, Jaime Sou Da, Lee, Pamela Pui Wah, Ho, Marco Hok Kung, Chung, Brian Hon Yin, Le, Huong Thi Minh, Yang, Wanling, Rohani, Pejman, Fouladvand, Ali, Rokni-Zadeh, Hassan, Changi-Ashtiani, Majid, Miryounesi, Mohammad, Puel, Anne, Shahrooei, Mohammad, Finocchi, Andrea, Rossi, Paolo, Rivalta, Beatrice, Cifaldi, Cristina, Novelli, Antonio, Passarelli, Chiara, Arasi, Stefania, Bullens, Dominique, Sauer, Kate, Claeys, Tania, Biggs, Catherine M., Morris, Emma C., Rosenzweig, Sergio D., O’Shea, John J., Wasserman, Wyeth W., Bedford, H. Melanie, van Karnebeek, Clara D.M., Palma, Paolo, Burns, Siobhan O., Meyts, Isabelle, Casanova, Jean-Laurent, Lyons, Jonathan J., Parvaneh, Nima, Nguyen, Anh Thi Van, Cancrini, Caterina, Heimall, Jennifer, Ahmed, Hanan, McKinnon, Margaret L., Lau, Yu Lung, Béziat, Vivien, Turvey, Stuart E.
Publicado 2023