Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosisIván K. Chinn,Olive S. Eckstein,Erin C. Peckham‐Gregory,Baruch Goldberg,Lisa R. Forbes,Sarah K. Nicholas,Emily M. Mace,Tiphanie P. Vogel,Harshal Abhyankar,María Alejandra Díaz,Helen E. Heslop,Robert A. Krance,Caridad Martinez,Trung C. Nguyen,Dalia Bashir, Joanne Goldman,Asbjørg Stray-Pedersen,Luis Alberto Pedroza,Cecilia Poli,Juan Carlos Aldave Becerra,Sean McGhee,Waleed Al‐Herz,Aghiad Chamdin,Zeynep Coban‐Akdemir,Shalini N. Jhangiani,Donna M. Muzny,Tram N. Cao,Diana N. Hong,Richard A. Gibbs,James R. Lupski,Jordan S. Orange,Kenneth L. McClain,Carl E. AllenBlood(2018)引用 107|浏览0暂无评分摘要Key Points Whole-exome sequencing may identify specific therapeutic opportunities for patients with HLH. HLH should be conceptualized as a critical illness phenotype driven by toxic activation of immune cells from different underlying mechanisms.更多查看译文关键词pediatric hemophagocytic lymphohistiocytosisAI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要