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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 3
2011 1
2012 2
2013 2
2014 5
2015 3
2016 3
2017 3
2019 2
2020 1
2021 2
2022 3
2023 1
2024 0

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27 results

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Page 1
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study.
Tromp TR, Hartgers ML, Hovingh GK, Vallejo-Vaz AJ, Ray KK, Soran H, Freiberger T, Bertolini S, Harada-Shiba M, Blom DJ, Raal FJ, Cuchel M; Homozygous Familial Hypercholesterolaemia International Clinical Collaborators. Tromp TR, et al. Lancet. 2022 Feb 19;399(10326):719-728. doi: 10.1016/S0140-6736(21)02001-8. Epub 2022 Jan 28. Lancet. 2022. PMID: 35101175 Free PMC article.
Circulating mucosal-associated invariant T cells identify patients responding to anti-PD-1 therapy.
De Biasi S, Gibellini L, Lo Tartaro D, Puccio S, Rabacchi C, Mazza EMC, Brummelman J, Williams B, Kaihara K, Forcato M, Bicciato S, Pinti M, Depenni R, Sabbatini R, Longo C, Dominici M, Pellacani G, Lugli E, Cossarizza A. De Biasi S, et al. Among authors: rabacchi c. Nat Commun. 2021 Mar 15;12(1):1669. doi: 10.1038/s41467-021-21928-4. Nat Commun. 2021. PMID: 33723257 Free PMC article.
Comparison of two polygenic risk scores to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects.
Cefalù AB, Spina R, Noto D, Rabacchi C, Giammanco A, Simone ML, Brucato F, Scrimali C, Gueli-Alletti MG, Barbagallo CM, Tarugi P, Averna MR. Cefalù AB, et al. Among authors: rabacchi c. J Clin Lipidol. 2022 Jul-Aug;16(4):530-537. doi: 10.1016/j.jacl.2022.04.009. Epub 2022 May 8. J Clin Lipidol. 2022. PMID: 35589500
Characterization of New ATM Deletion Associated with Hereditary Breast Cancer.
Parenti S, Rabacchi C, Marino M, Tenedini E, Artuso L, Castellano S, Carretta C, Mallia S, Cortesi L, Toss A, Barbieri E, Manfredini R, Luppi M, Trenti T, Tagliafico E. Parenti S, et al. Among authors: rabacchi c. Genes (Basel). 2021 Jan 21;12(2):136. doi: 10.3390/genes12020136. Genes (Basel). 2021. PMID: 33494414 Free PMC article.
Novel mutations of SAR1B gene in four children with chylomicron retention disease.
Simone ML, Rabacchi C, Kuloglu Z, Kansu A, Ensari A, Demir AM, Hizal G, Di Leo E, Bertolini S, Calandra S, Tarugi P. Simone ML, et al. Among authors: rabacchi c. J Clin Lipidol. 2019 Jul-Aug;13(4):554-562. doi: 10.1016/j.jacl.2019.05.013. Epub 2019 May 30. J Clin Lipidol. 2019. PMID: 31253576
27 results