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The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder.
Holland A, Whittington J, Cohen O, Curfs L, Delahaye F, Dudley O, Horsthemke B, Lindgren AC, Nourissier C, Sharma N, Vogels A. Holland A, et al. Among authors: cohen o. J Intellect Disabil Res. 2009 Jun;53(6):538-47. doi: 10.1111/j.1365-2788.2009.01172.x. Epub 2009 Apr 23. J Intellect Disabil Res. 2009. PMID: 19457156
Low recurrence rates for challenging squamous cell carcinomas using Mohs micrographic surgery with AE1/AE3 cytokeratin immunostaining.
Aizman L, Miller CJ, Perz AM, Lukowiak TM, Cohen OG, Bean E, Hitchner MK, Etzkorn JR, Shin TM, Higgins HW 2nd, Giordano CN, Cohen JV, Miura JT, Sobanko JF. Aizman L, et al. J Am Acad Dermatol. 2021 May;84(5):1453-1455. doi: 10.1016/j.jaad.2020.06.1012. Epub 2020 Jul 3. J Am Acad Dermatol. 2021. PMID: 32622892 No abstract available.
Preliminary report from the World Health Organisation Chest Radiography in Epidemiological Studies project.
Mahomed N, Fancourt N, de Campo J, de Campo M, Akano A, Cherian T, Cohen OG, Greenberg D, Lacey S, Kohli N, Lederman HM, Madhi SA, Manduku V, McCollum ED, Park K, Ribo-Aristizabal JL, Bar-Zeev N, O'Brien KL, Mulholland K. Mahomed N, et al. Among authors: cohen og, o brien kl. Pediatr Radiol. 2017 Oct;47(11):1399-1404. doi: 10.1007/s00247-017-3834-9. Epub 2017 Sep 21. Pediatr Radiol. 2017. PMID: 29043423 Free PMC article. Review.
1,164 results