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

Year Number of Results
1979 1
1980 2
1990 2
1991 1
1992 2
1993 2
1994 1
1995 2
1998 1
2005 1
2010 2
2011 2
2012 1
2013 2
2015 1
2016 2
2018 2
2019 1
2020 1
2022 1
2024 0

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27 results

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Page 1
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny.
Tannorella P, Calzari L, Daolio C, Mainini E, Vimercati A, Gentilini D, Soli F, Pedrolli A, Bonati MT, Larizza L, Russo S. Tannorella P, et al. Among authors: mainini e. Clin Epigenetics. 2022 Mar 22;14(1):43. doi: 10.1186/s13148-022-01262-2. Clin Epigenetics. 2022. PMID: 35317853 Free PMC article.
[Oral contraception and multiple sclerosis].
Ghezzi A, Caputo D, Manara F, Mainini E. Ghezzi A, et al. Among authors: mainini e. Arch Sci Med (Torino). 1979 Jan-Mar;136(1):67-73. Arch Sci Med (Torino). 1979. PMID: 380517 Review. Italian.
Ground states in the diffusion-dominated regime.
Carrillo JA, Hoffmann F, Mainini E, Volzone B. Carrillo JA, et al. Among authors: mainini e. Calc Var Partial Differ Equ. 2018;57(5):127. doi: 10.1007/s00526-018-1402-2. Epub 2018 Aug 11. Calc Var Partial Differ Equ. 2018. PMID: 30393443 Free PMC article.
N 3 / 4 Law in the Cubic Lattice.
Mainini E, Piovano P, Schmidt B, Stefanelli U. Mainini E, et al. J Stat Phys. 2019;176(6):1480-1499. doi: 10.1007/s10955-019-02350-z. Epub 2019 Jul 24. J Stat Phys. 2019. PMID: 31555015 Free PMC article.
Treatments and prescriptions in advanced dementia patients residing in long-term care institutions and at home.
Toscani F, Di Giulio P, Villani D, Giunco F, Brunelli C, Gentile S, Finetti S, Charrier L, Monti M, van der Steen JT; End of Life Observatory-Prospective Study on Dementia Patients Care Research Group. Toscani F, et al. J Palliat Med. 2013 Jan;16(1):31-7. doi: 10.1089/jpm.2012.0165. Epub 2012 Dec 12. J Palliat Med. 2013. PMID: 23234299 Free article. No abstract available.
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MT, Melis D, Manfredini E, Ferrero GB, Pecile V, Larizza L. Russo S, et al. Among authors: mainini e. Clin Epigenetics. 2016 Mar 1;8:23. doi: 10.1186/s13148-016-0183-8. eCollection 2016. Clin Epigenetics. 2016. PMID: 26933465 Free PMC article.
27 results