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Page 1
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Genet Med. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. Online ahead of print. Genet Med. 2024. PMID: 39033378 Free article.
Cultural evolution and prehistoric demography.
Strassberg SS, Creanza N. Strassberg SS, et al. Philos Trans R Soc Lond B Biol Sci. 2021 Jan 18;376(1816):20190713. doi: 10.1098/rstb.2019.0713. Epub 2020 Nov 30. Philos Trans R Soc Lond B Biol Sci. 2021. PMID: 33250027 Free PMC article. Review.
The genetic basis for bronchopulmonary dysplasia.
Parton LA, Strassberg SS, Qian D, Galvin-Parton PA, Cristea IA. Parton LA, et al. Among authors: strassberg ss. Front Biosci. 2006 May 1;11:1854-60. doi: 10.2741/1928. Front Biosci. 2006. PMID: 16368561
Early survival and safety of ALPPS: first report of the International ALPPS Registry.
Schadde E, Ardiles V, Robles-Campos R, Malago M, Machado M, Hernandez-Alejandro R, Soubrane O, Schnitzbauer AA, Raptis D, Tschuor C, Petrowsky H, De Santibanes E, Clavien PA; ALPPS Registry Group. Schadde E, et al. Ann Surg. 2014 Nov;260(5):829-36; discussion 836-8. doi: 10.1097/SLA.0000000000000947. Ann Surg. 2014. PMID: 25379854 Free article.