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Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy.
Donkervoort S, Mohassel P, O'Leary M, Bonner DE, Hartley T, Acquaye N, Brull A, Mozaffar T, Saporta MA, Dyment DA, Sampson JB, Pajusalu S, Austin-Tse C, Hurth K, Cohen JS, McWalter K, Warman-Chardon J, Crunk A, Foley AR; Undiagnosed Diseases Network; Mammen AL, Wheeler MT, O'Donnell-Luria A, Bönnemann CG. Donkervoort S, et al. Among authors: hartley t. Ann Clin Transl Neurol. 2024 Mar;11(3):629-640. doi: 10.1002/acn3.51983. Epub 2024 Feb 4. Ann Clin Transl Neurol. 2024. PMID: 38311799 Free PMC article.
A Modular Biosensor Design for Quantitative Measurement of Free Nedd8.
Davis ZW, Coyle K, Park MK, Oren T, Hartley T, Umphlett A, Monahan J, Light K, Hunter K, Choi YS. Davis ZW, et al. Among authors: hartley t. ACS Sens. 2024 Sep 27;9(9):4740-4747. doi: 10.1021/acssensors.4c01130. Epub 2024 Sep 10. ACS Sens. 2024. PMID: 39253816 Free PMC article.
Clinical decision aids and computed tomography coronary angiography in patients with suspected acute coronary syndrome.
Wang KL, Taggart C, McDermott M, O'Brien R, Oatey K, Keating L, Storey RF, Felmeden D, Curzen N, Kardos A, Roobottom C, Smith J, Goodacre S, Newby DE, Gray AJ; RAPID-CTCA Investigators. Wang KL, et al. Emerg Med J. 2024 Jul 22;41(8):488-494. doi: 10.1136/emermed-2024-213904. Emerg Med J. 2024. PMID: 38857986 Free article. Clinical Trial.
337 results