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

Year Number of Results
2007 2
2008 1
2009 3
2010 3
2011 2
2012 1
2014 3
2015 2
2016 2
2017 1
2018 2
2019 2
2020 2
2021 4
2022 8
2023 4
2024 2

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38 results

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Page 1
Tertiary and Postrenal Transplantation Hyperparathyroidism.
Alfieri C, Mattinzoli D, Messa P. Alfieri C, et al. Among authors: mattinzoli d. Endocrinol Metab Clin North Am. 2021 Dec;50(4):649-662. doi: 10.1016/j.ecl.2021.08.004. Endocrinol Metab Clin North Am. 2021. PMID: 34774239 Review.
Is there a role in acute kidney injury for FGF23 and Klotho?
Mattinzoli D, Molinari P, Romero-González G, Bover J, Cicero E, Pesce F, Abinti M, Conti C, Castellano G, Alfieri C. Mattinzoli D, et al. Clin Kidney J. 2023 Apr 25;16(10):1555-1562. doi: 10.1093/ckj/sfad093. eCollection 2023 Oct. Clin Kidney J. 2023. PMID: 37779849 Free PMC article. Review.
Podocytes: recent biomolecular developments.
Armelloni S, Corbelli A, Giardino L, Li M, Ikehata M, Mattinzoli D, Messa P, Pignatari C, Watanabe S, Rastaldi MP. Armelloni S, et al. Among authors: mattinzoli d. Biomol Concepts. 2014 Aug;5(4):319-30. doi: 10.1515/bmc-2014-0020. Biomol Concepts. 2014. PMID: 25372762 Free article. Review.
Carbon dots conjugated to SN38 for improved colorectal anticancer therapy.
Mattinzoli D, Cacioppo M, Ikehata M, Armelloni S, Alfieri CM, Castellano G, Barilani M, Arcudi F, Messa P, Prato M. Mattinzoli D, et al. Mater Today Bio. 2022 Sep 1;16:100286. doi: 10.1016/j.mtbio.2022.100286. eCollection 2022 Dec. Mater Today Bio. 2022. PMID: 36186846 Free PMC article.
Expression of interferon-stimulated gene 20 (ISG20), an antiviral effector protein, in glomerular endothelial cells: possible involvement of ISG20 in lupus nephritis.
Karasawa T, Sato R, Imaizumi T, Fujita M, Aizawa T, Tsugawa K, Mattinzoli D, Kawaguchi S, Seya K, Terui K, Joh K, Tanaka H. Karasawa T, et al. Among authors: mattinzoli d. Ren Fail. 2023 Dec;45(1):2224890. doi: 10.1080/0886022X.2023.2224890. Ren Fail. 2023. PMID: 37340981 Free PMC article.
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly.
Elli FM, Mattinzoli D, Lucca C, Piu M, Maffini MA, Costanza J, Fontana L, Santaniello C, Forino C, Milani D, Bonati MT, Secco A, Gastaldi R, Alfieri C, Messa P, Miozzo M, Arosio M, Mantovani G. Elli FM, et al. Among authors: mattinzoli d. J Bone Miner Res. 2022 Mar;37(3):465-474. doi: 10.1002/jbmr.4490. Epub 2022 Jan 17. J Bone Miner Res. 2022. PMID: 34897794 Free PMC article.
38 results