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A Systematic Review and Meta-Analysis of Mapping Biopsy for Primary Extramammary Paget's Disease in Reducing Recurrence Following Surgical Excision.
Murugan T, Wong LCK, Ong XS, Tan SH, Tan JW, Liu Y, Shannon NB, Chiang J, Poon E, Chan JY, Yang VS, Somasundaram N, Farid M, Wong RX, Nei WL, Kwek JW, Thng CH, Hennedige T, Tang PY, Selvarajan S, Tay KJ, Abdul MR, Wong JSM, Seo CJ, Soo KC, Chia CS, Ong CJ. Murugan T, et al. Among authors: shannon nb. Ann Surg Open. 2023 Nov 2;4(4):e339. doi: 10.1097/AS9.0000000000000339. eCollection 2023 Dec. Ann Surg Open. 2023. PMID: 38144489 Free PMC article.
Prehabilitation programs - a systematic review of the economic evidence.
Ke Y, Ng RRG, Elangovan S, Leong YH, Goh ZH, Graves N, Shannon NB, Abdullah HR. Ke Y, et al. Among authors: shannon nb. Front Med (Lausanne). 2023 Dec 1;10:1281843. doi: 10.3389/fmed.2023.1281843. eCollection 2023. Front Med (Lausanne). 2023. PMID: 38105890 Free PMC article.
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Jeffries L, Mis EK, McWalter K, Donkervoort S, Brodsky NN, Carpier JM, Ji W, Ionita C, Roy B, Morrow JS, Darbinyan A, Iyer K, Aul RB, Banka S, Chao KR, Cobbold L, Cohen S, Custodio HM, Drummond-Borg M, Elmslie F, Finanger E, Hainline BE, Helbig I, Hewson S, Hu Y, Jackson A, Josifova D, Konstantino M, Leach ME, Mak B, McCormick D, McGee E, Nelson S, Nguyen J, Nugent K, Ortega L, Goodkin HP, Roeder E, Roy S, Sapp K, Saade D, Sisodiya SM, Stals K, Towner S, Wilson W; Deciphering Developmental Disorders; Genomics England Research Consortium; Undiagnosed Disease Network; Khokha MK, Bönnemann CG, Lucas CL, Lakhani SA. Jeffries L, et al. Genet Med. 2024 Feb;26(2):101023. doi: 10.1016/j.gim.2023.101023. Epub 2023 Nov 7. Genet Med. 2024. PMID: 37947183
Nephrectomy for xanthogranulomatous pyelonephritis-a not-so-simple solution.
Kelly C, Anderson S, Looney A, Shannon N, Senaratne R, O'Connor E, Breen K, Lennon G, McGuire B, Murphy M, Moran D, Galvin D. Kelly C, et al. Among authors: shannon n. Ir J Med Sci. 2024 Apr;193(2):1055-1060. doi: 10.1007/s11845-023-03496-2. Epub 2023 Aug 23. Ir J Med Sci. 2024. PMID: 37610600 Free PMC article.
Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.
Wright CF, Campbell P, Eberhardt RY, Aitken S, Perrett D, Brent S, Danecek P, Gardner EJ, Chundru VK, Lindsay SJ, Andrews K, Hampstead J, Kaplanis J, Samocha KE, Middleton A, Foreman J, Hobson RJ, Parker MJ, Martin HC, FitzPatrick DR, Hurles ME, Firth HV; DDD Study. Wright CF, et al. N Engl J Med. 2023 Apr 27;388(17):1559-1571. doi: 10.1056/NEJMoa2209046. Epub 2023 Apr 12. N Engl J Med. 2023. PMID: 37043637 Free PMC article.
148 results