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Surface-Enhanced Raman Spectroscopy Chips Based on Silver Coated Gold Nanostars.
Parmigiani M, Albini B, Pellegrini G, Genovesi M, De Vita L, Pallavicini P, Dacarro G, Galinetto P, Taglietti A. Parmigiani M, et al. Among authors: genovesi m. Nanomaterials (Basel). 2022 Oct 14;12(20):3609. doi: 10.3390/nano12203609. Nanomaterials (Basel). 2022. PMID: 36296798 Free PMC article.
In the Global Epicenter: Social Work Leadership in a New York City Hospital.
Xenakis N, Brosnan MM, Burgos L, Childs J, Deschamps J, Dobrof J, Farquhar DW, Genovesi ML, Goldgraben KR, Gordon E, Hamilton C, Koppel SR, Lipp MN, Potter R, Rauch A, Rodriguez V, Schubert E, Sollars ED, Zilberfein F. Xenakis N, et al. Among authors: genovesi ml. Soc Work Health Care. 2021;60(1):62-77. doi: 10.1080/00981389.2021.1885563. Epub 2021 Feb 15. Soc Work Health Care. 2021. PMID: 33588694
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance.
Traversa A, Marchionni E, Giovannetti A, Genovesi ML, Panzironi N, Margiotti K, Napoli G, Piceci Sparascio F, De Luca A, Petrizzelli F, Carella M, Cardona F, Bernardo S, Manganaro L, Mazza T, Pizzuti A, Caputo V. Traversa A, et al. Among authors: genovesi ml. Mol Genet Genomic Med. 2020 Aug;8(8):e1336. doi: 10.1002/mgg3.1336. Epub 2020 Jun 10. Mol Genet Genomic Med. 2020. PMID: 32519823 Free PMC article.
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation.
Traversa A, Bernardo S, Paiardini A, Giovannetti A, Marchionni E, Genovesi ML, Guadagnolo D, Torres B, Paolacci S, Bernardini L, Mazza T, Carella M, Caputo V, Pizzuti A. Traversa A, et al. Among authors: genovesi ml. Mol Genet Genomic Med. 2020 Jan;8(1):e1054. doi: 10.1002/mgg3.1054. Epub 2019 Nov 22. Mol Genet Genomic Med. 2020. PMID: 31756055 Free PMC article.
50 results