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Results by year

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

Year Number of Results
1994 1
1997 3
1998 1
1999 4
2000 2
2001 5
2004 1
2005 9
2006 7
2007 9
2008 5
2009 7
2010 2
2011 3
2012 5
2014 4
2015 7
2016 2
2017 2
2018 6
2019 8
2020 1
2021 1
2022 3
2023 1
2024 0

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Search Results

91 results

Results by year

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Page 1
Molecular genetics for familial hypercholesterolemia.
Marziliano N, Medoro A, Folzani S, Intrieri M, Reverberi C. Marziliano N, et al. Rev Cardiovasc Med. 2022 Jan 8;23(1):4. doi: 10.31083/j.rcm2301004. Rev Cardiovasc Med. 2022. PMID: 35092196 Free article. No abstract available.
Role of cardiac imaging in Anderson-Fabry cardiomyopathy.
Serra W, Marziliano N. Serra W, et al. Among authors: marziliano n. Cardiovasc Ultrasound. 2019 Jan 23;17(1):1. doi: 10.1186/s12947-019-0151-5. Cardiovasc Ultrasound. 2019. PMID: 30674321 Free PMC article. Review.
Proteases Upregulation in Sporadic Alzheimer's Disease Brain.
Medoro A, Bartollino S, Mignogna D, Marziliano N, Porcile C, Nizzari M, Florio T, Pagano A, Raimo G, Intrieri M, Russo C. Medoro A, et al. Among authors: marziliano n. J Alzheimers Dis. 2019;68(3):931-938. doi: 10.3233/JAD-181284. J Alzheimers Dis. 2019. PMID: 30814362
EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder.
Lévy J, Haye D, Marziliano N, Casu G, Guimiot F, Dupont C, Teissier N, Benzacken B, Gressens P, Pipiras E, Verloes A, Tabet AC. Lévy J, et al. Among authors: marziliano n. Clin Genet. 2018 Jun;93(6):1141-1147. doi: 10.1111/cge.13234. Epub 2018 Mar 15. Clin Genet. 2018. PMID: 29508392
An Impressive Case of "Honeycomb" In-Stent Restenosis.
Lorenzoni G, Merella P, Viola G, Marziliano N, Casu G. Lorenzoni G, et al. Among authors: marziliano n. J Invasive Cardiol. 2018 Sep;30(9):E99. J Invasive Cardiol. 2018. PMID: 30158330 Free article.
Gene symbol: LDB3.
Arbustini E, Rossi ML, Marziliano N, Presbitero P, Pilotto A, Pasotti M, Grasso M. Arbustini E, et al. Among authors: marziliano n. Hum Genet. 2007 Feb;120(6):910. Hum Genet. 2007. PMID: 17438604 No abstract available.
Aneurysm syndromes and TGF-beta receptor mutations.
Arbustini E, Marziliano N, Magrassi L. Arbustini E, et al. Among authors: marziliano n. N Engl J Med. 2006 Nov 16;355(20):2155; author reply 2156. doi: 10.1056/NEJMc062573. N Engl J Med. 2006. PMID: 17108349 No abstract available.
91 results