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[PROFILES: typical portrait of the future Swiss doctors].
Bart PA, Monti M, Gachoud D, Félix S, Turpin D, Marino L, Takeuchi YL, Senn N, Sohrmann M. Bart PA, et al. Among authors: marino l. Rev Med Suisse. 2020 Jan 22;16(678):133-137. Rev Med Suisse. 2020. PMID: 31967756 French.
[Hospital-based internal medicine: year 2011 in chief resident's perspective].
Garnier A, Barberini L, Castioni J, Cosma Rochat M, Gachoud D, Gagliano M, Gianinazzi F, Joly Schwartz C, Marino L, Merz L, Rochat M, Stadelmann R, Urbano LA. Garnier A, et al. Among authors: marino l. Rev Med Suisse. 2012 Feb 1;8(326):254-8. Rev Med Suisse. 2012. PMID: 22364073 French.
Subclinical hypothyroidism: new trials, old caveats.
Lamine F, De Giorgi S, Marino L, Michalaki M, Sykiotis GP. Lamine F, et al. Among authors: marino l. Hormones (Athens). 2018 Jun;17(2):231-236. doi: 10.1007/s42000-018-0004-x. Epub 2018 Apr 27. Hormones (Athens). 2018. PMID: 29858848 Review.
Papillary thyroid carcinoma with nodular fasciitis-like stroma and β-catenin mutations should be renamed papillary thyroid carcinoma with desmoid-type fibromatosis.
Rebecchini C, Nobile A, Piana S, Sarro R, Bisig B, Gerasimos SP, Saglietti C, Matter M, Marino L, Bongiovanni M. Rebecchini C, et al. Among authors: marino l. Mod Pathol. 2017 Feb;30(2):236-245. doi: 10.1038/modpathol.2016.173. Epub 2016 Oct 7. Mod Pathol. 2017. PMID: 27713418 Free article.
Very low expression of PD-L1 in medullary thyroid carcinoma.
Bongiovanni M, Rebecchini C, Saglietti C, Bulliard JL, Marino L, de Leval L, Sykiotis GP. Bongiovanni M, et al. Among authors: marino l. Endocr Relat Cancer. 2017 Jun;24(6):L35-L38. doi: 10.1530/ERC-17-0104. Epub 2017 Apr 18. Endocr Relat Cancer. 2017. PMID: 28420659 Free PMC article. No abstract available.
Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants.
Xu C, Cassatella D, van der Sloot AM, Quinton R, Hauschild M, De Geyter C, Flück C, Feller K, Bartholdi D, Nemeth A, Halperin I, Pekic Djurdjevic S, Maeder P, Papadakis G, Dwyer AA, Marino L, Favre L, Pignatelli D, Niederländer NJ, Acierno J, Pitteloud N. Xu C, et al. Among authors: marino l. Genet Med. 2018 Aug;20(8):872-881. doi: 10.1038/gim.2017.197. Epub 2017 Nov 16. Genet Med. 2018. PMID: 29144511 Free article.
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.
Bouilly J, Messina A, Papadakis G, Cassatella D, Xu C, Acierno JS, Tata B, Sykiotis G, Santini S, Sidis Y, Elowe-Gruau E, Phan-Hug F, Hauschild M, Bouloux PM, Quinton R, Lang-Muritano M, Favre L, Marino L, Giacobini P, Dwyer AA, Niederländer NJ, Pitteloud N. Bouilly J, et al. Among authors: marino l. Hum Mol Genet. 2018 Jan 15;27(2):359-372. doi: 10.1093/hmg/ddx408. Hum Mol Genet. 2018. PMID: 29202173
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