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Protection or susceptibility to devastating childhood epilepsy: Nodding Syndrome associates with immunogenetic fingerprints in the HLA binding groove.
Benedek G, Abed El Latif M, Miller K, Rivkin M, Ramadhan Lasu AA, Riek LP, Lako R, Edvardson S, Alon SA, Galun E, Levite M. Benedek G, et al. Among authors: miller k. PLoS Negl Trop Dis. 2020 Jul 8;14(7):e0008436. doi: 10.1371/journal.pntd.0008436. eCollection 2020 Jul. PLoS Negl Trop Dis. 2020. PMID: 32639997 Free PMC article.
Macrophage migration inhibitory factor in Nodding syndrome.
Benedek G, Abed El Latif M, Miller K, Rivkin M, Ahmed Ramadhan Lasu A, P Riek L, Lako R, Edvardson S, Arbel-Alon S, Galun E, Levite M. Benedek G, et al. Among authors: miller k. PLoS Negl Trop Dis. 2021 Oct 18;15(10):e0009821. doi: 10.1371/journal.pntd.0009821. eCollection 2021 Oct. PLoS Negl Trop Dis. 2021. PMID: 34662363 Free PMC article.
MIF -173G/C polymorphism is associated with NMO disease severity.
Brill L, Vaknin-Dembinsky A, Zveik O, Haham N, Miller K, Benedek G. Brill L, et al. Among authors: miller k. J Neuroimmunol. 2020 Feb 15;339:577120. doi: 10.1016/j.jneuroim.2019.577120. Epub 2019 Nov 25. J Neuroimmunol. 2020. PMID: 31790982
Changing Treatment and Metastatic Disease Patterns in Patients with EGFR Mutated NSCLC: An Academic Thoracic Medical Investigator's Consortium Registry Analysis.
Stalker M, Grady CB, Watts A, Hwang WT, Chandrasekhara K, Sun F, Liu G, Patel D, Nieva J, Herrmann A, Marrone K, Lam VK, Velcheti V, Liu SV, Bravo Montenegro GL, Tompkins W, Patil T, Weiss J, Miller KL, Schwartzman W, Dowell JE, Shaverdashvili K, Villaruz L, Cass A, Iams W, Aisner D, Aggarwal C, Camidge DR, Sun L, Marmarelis ME. Stalker M, et al. Among authors: miller kl. JTO Clin Res Rep. 2024 Nov 12;6(1):100765. doi: 10.1016/j.jtocrr.2024.100765. eCollection 2025 Jan. JTO Clin Res Rep. 2024. PMID: 39758601 Free PMC article.
7,793 results