A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70

por Chan, Alice Y., Punwani, Divya, Kadlecek, Theresa A., Cowan, Morton J., Olson, Jean L., Mathes, Erin F., Sunderam, Uma, Man Fu, Shu, Srinivasan, Rajgopal, Kuriyan, John, Brenner, Steven E., Weiss, Arthur, Puck, Jennifer M.
Publicado 2016

Development of SkinTracker, an integrated dermatology mobile app and web portal enabling remote clinical research studies

por Jin, Joy Q., Hong, Julie, Elhage, Kareem G., Braun, Mitchell, Spencer, Riley K., Chung, Mimi, Yeroushalmi, Samuel, Hadeler, Edward, Mosca, Megan, Bartholomew, Erin, Hakimi, Marwa, Davis, Mitchell S., Thibodeaux, Quinn, Wu, David, Kahlon, Abhilash, Dhaliwal, Paul, Mathes, Erin F., Dhaliwal, Navdeep, Bhutani, Tina, Liao, Wilson
Publicado 2023

S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis‐like syndrome

por Chen, Fuying, Ni, Cheng, Wang, Xiaoxiao, Cheng, Ruhong, Pan, Chaolan, Wang, Yumeng, Liang, Jianying, Zhang, Jia, Cheng, Jinke, Chin, Y Eugene, Zhou, Yi, Wang, Zhen, Guo, Yiran, Chen, She, Htun, Stephanie, Mathes, Erin F, de Alba Campomanes, Alejandra G, Slavotinek, Anne M, Zhang, Si, Li, Ming, Yao, Zhirong
Publicado 2022

Consensus recommendations for the use of retinoids in ichthyosis and other disorders of cornification in children and adolescents

por Zaenglein, Andrea L., Levy, Moise L., Stefanko, Nicole S., Benjamin, Latanya T., Bruckner, Anna L., Choate, Keith, Craiglow, Brittany G., DiGiovanna, John J., Eichenfield, Lawrence F., Elias, Peter, Fleckman, Philip, Lawley, Leslie P., Lewis, Richard A., Lucky, Anne W., Mathes, Erin F., Milstone, Leonard M., Paller, Amy S., Patel, Sonali S., Siegel, Dawn H., Teng, Joyce, Tanumihardjo, Sherry A., Thaxton, Lauren, Williams, Mary L.
Publicado 2020