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2018 4
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2020 2
2021 3
2024 1

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Page 1
MICB Genomic Variant Is Associated with NKG2D-mediated Acute Lung Injury and Death.
Aguilar OA, Qualls AE, Gonzalez-Hinojosa MDR, Obeidalla S, Kerchberger VE, Tsao T, Singer JP, Looney MR, Raymond W, Hays SR, Golden JA, Kukreja J, Shaver CM, Ware LB, Christie J, Diamond JM, Lanier LL, Greenland JR, Calabrese DR. Aguilar OA, et al. Among authors: qualls ae. Am J Respir Crit Care Med. 2024 Jan 1;209(1):70-82. doi: 10.1164/rccm.202303-0472OC. Am J Respir Crit Care Med. 2024. PMID: 37878820
Novel SPEG mutations in congenital myopathies: Genotype-phenotype correlations.
Qualls AE, Donkervoort S, Herkert JC, D'gama AM, Bharucha-Goebel D, Collins J, Chao KR, Foley AR, Schoots MH, Jongbloed JDH, Bönnemann CG, Agrawal PB. Qualls AE, et al. Muscle Nerve. 2019 Mar;59(3):357-362. doi: 10.1002/mus.26378. Epub 2018 Nov 28. Muscle Nerve. 2019. PMID: 30412272 Free PMC article.
Novel founder intronic variant in SLC39A14 in two families causing Manganism and potential treatment strategies.
Rodan LH, Hauptman M, D'Gama AM, Qualls AE, Cao S, Tuschl K, Al-Jasmi F, Hertecant J, Hayflick SJ, Wessling-Resnick M, Yang ET, Berry GT, Gropman A, Woolf AD, Agrawal PB. Rodan LH, et al. Among authors: qualls ae. Mol Genet Metab. 2018 Jun;124(2):161-167. doi: 10.1016/j.ymgme.2018.04.002. Epub 2018 Apr 6. Mol Genet Metab. 2018. PMID: 29685658 Free PMC article.
11 results