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Year Number of Results
1991 1
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2001 1
2002 2
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2006 3
2007 6
2008 1
2009 1
2010 4
2011 2
2013 3
2014 1
2015 4
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73 results

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Page 1
Liraglutide in Children and Adolescents with Type 2 Diabetes.
Tamborlane WV, Barrientos-Pérez M, Fainberg U, Frimer-Larsen H, Hafez M, Hale PM, Jalaludin MY, Kovarenko M, Libman I, Lynch JL, Rao P, Shehadeh N, Turan S, Weghuber D, Barrett T; Ellipse Trial Investigators. Tamborlane WV, et al. N Engl J Med. 2019 Aug 15;381(7):637-646. doi: 10.1056/NEJMoa1903822. Epub 2019 Apr 28. N Engl J Med. 2019. PMID: 31034184 Clinical Trial.
Declaration of Lisbon.
Limbert C, Wood J, Hofer S, Svensson J, Cameron F, Cardona-Hernandez R, Lion S, Maahs DM. Limbert C, et al. Lancet Diabetes Endocrinol. 2024 Nov;12(11):789. doi: 10.1016/S2213-8587(24)00305-X. Epub 2024 Oct 16. Lancet Diabetes Endocrinol. 2024. PMID: 39423841 No abstract available.
Personalizing Early-Stage Type 1 Diabetes in Children.
Limbert C, von dem Berge T, Danne T. Limbert C, et al. Diabetes Care. 2023 Oct 1;46(10):1747-1749. doi: 10.2337/dci23-0025. Diabetes Care. 2023. PMID: 37729506 No abstract available.
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism.
Wakeling MN, Owens NDL, Hopkinson JR, Johnson MB, Houghton JAL, Dastamani A, Flaxman CS, Wyatt RC, Hewat TI, Hopkins JJ, Laver TW, van Heugten R, Weedon MN, De Franco E, Patel KA, Ellard S, Morgan NG, Cheesman E, Banerjee I, Hattersley AT, Dunne MJ; International Congenital Hyperinsulinism Consortium; Richardson SJ, Flanagan SE. Wakeling MN, et al. Nat Genet. 2022 Nov;54(11):1615-1620. doi: 10.1038/s41588-022-01204-x. Epub 2022 Nov 4. Nat Genet. 2022. PMID: 36333503 Free PMC article.
Non-adenomatous sellar lesions: single-centre 10-year experience.
Sousa Santos F, Nunes Dias L, Henriques V, Canas Marques C, Chorão M, Sequeira Duarte J, Limbert C, Costa J, Graça J, Vasconcelos C, Cabral J, Ramos S. Sousa Santos F, et al. Among authors: limbert c. Hormones (Athens). 2018 Dec;17(4):557-563. doi: 10.1007/s42000-018-0064-y. Epub 2018 Oct 3. Hormones (Athens). 2018. PMID: 30284206
Genetic architecture of congenital hypogonadotropic hypogonadism: insights from analysis of a Portuguese cohort.
Carriço JN, Gonçalves CI, Al-Naama A, Syed N, Aragüés JM, Bastos M, Fonseca F, Borges T, Pereira BD, Pignatelli D, Carvalho D, Cunha F, Saavedra A, Rodrigues E, Saraiva J, Ruas L, Vicente N, Martin Martins J, De Sousa Lages A, Oliveira MJ, Castro-Correia C, Melo M, Martins RG, Couto J, Moreno C, Martins D, Oliveira P, Martins T, Martins SA, Marques O, Meireles C, Garrão A, Nogueira C, Baptista C, Gama-de-Sousa S, Amaral C, Martinho M, Limbert C, Barros L, Vieira IH, Sabino T, Saraiva LR, Lemos MC. Carriço JN, et al. Among authors: limbert c. Hum Reprod Open. 2024 Sep 11;2024(3):hoae053. doi: 10.1093/hropen/hoae053. eCollection 2024. Hum Reprod Open. 2024. PMID: 39308770 Free PMC article.
73 results