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A case of neonatal sweet syndrome associated with mevalonate kinase deficiency.
Irwin M, Tanawattanacharoen VK, Turner A, Son MBF, Hale RC, Platt CD, Putra J, Schmidt BAR, Wasserman MG. Irwin M, et al. Among authors: turner a. Pediatr Rheumatol Online J. 2023 Sep 12;21(1):101. doi: 10.1186/s12969-023-00887-8. Pediatr Rheumatol Online J. 2023. PMID: 37700301 Free PMC article.
Unique and shared systemic biomarkers for emphysema in Alpha-1 Antitrypsin deficiency and chronic obstructive pulmonary disease.
Serban KA, Pratte KA, Strange C, Sandhaus RA, Turner AM, Beiko T, Spittle DA, Maier L, Hamzeh N, Silverman EK, Hobbs BD, Hersh CP, DeMeo DL, Cho MH, Bowler RP. Serban KA, et al. Among authors: turner am. EBioMedicine. 2022 Oct;84:104262. doi: 10.1016/j.ebiom.2022.104262. Epub 2022 Sep 22. EBioMedicine. 2022. PMID: 36155958 Free PMC article.
The IFITM5 mutation in osteogenesis imperfecta type V is associated with an ERK/SOX9-dependent osteoprogenitor differentiation defect.
Marom R, Song IW, Busse EC, Washington ME, Berrier AS, Rossi VC, Ortinau L, Jeong Y, Jiang MM, Dawson BC, Adeyeye M, Leynes C, Lietman CD, Stroup BM, Batkovskyte D, Jain M, Chen Y, Cela R, Castellon A, Tran AA, Lorenzo I, Meyers DN, Huang S, Turner A, Shenava V, Wallace M, Orwoll E, Park D, Ambrose CG, Nagamani SC, Heaney JD, Lee BH. Marom R, et al. Among authors: turner a. J Clin Invest. 2024 Jun 11:e170369. doi: 10.1172/JCI170369. Online ahead of print. J Clin Invest. 2024. PMID: 38885336
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 Jun 10:emermed-2024-213904. doi: 10.1136/emermed-2024-213904. Online ahead of print. Emerg Med J. 2024. PMID: 38857986
4,199 results