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Page 1
Amniotic fluid stem cell exosomes: Therapeutic perspective.
Beretti F, Zavatti M, Casciaro F, Comitini G, Franchi F, Barbieri V, La Sala GB, Maraldi T. Beretti F, et al. Among authors: barbieri v. Biofactors. 2018 Mar;44(2):158-167. doi: 10.1002/biof.1407. Epub 2018 Jan 16. Biofactors. 2018. PMID: 29341292
Prenatal Detection of Vesico-Allantoic Cyst: Ultrasound and Autopsy Findings.
Bonasoni MP, Comitini G, Cavicchioni O, Barbieri V, Dalla Dea G, Palicelli A, Aguzzoli L. Bonasoni MP, et al. Among authors: barbieri v. Fetal Pediatr Pathol. 2023 Jun;42(3):498-505. doi: 10.1080/15513815.2022.2143250. Epub 2022 Nov 11. Fetal Pediatr Pathol. 2023. PMID: 36369825
Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous Couples.
Peluso F, Caraffi SG, Zuntini R, Trimarchi G, Ivanovski I, Valeri L, Barbieri V, Marinelli M, Pancaldi A, Melli N, Cesario C, Agolini E, Cellini E, Radio FC, Crisafi A, Napoli M, Guerrini R, Tartaglia M, Novelli A, Gargano G, Zuffardi O, Garavelli L. Peluso F, et al. Among authors: barbieri v. Genes (Basel). 2021 Jun 24;12(7):962. doi: 10.3390/genes12070962. Genes (Basel). 2021. PMID: 34202629 Free PMC article.
Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the SOX2 Gene: Ultrasound, Pathological, and Cytogenetic Findings.
Bonasoni MP, Comitini G, Pati M, Bizzarri V, Barbieri V, Marinelli M, Caraffi SG, Zuntini R, Pollazzon M, Palicelli A, Garavelli L. Bonasoni MP, et al. Among authors: barbieri v. Fetal Pediatr Pathol. 2023 Dec;42(6):979-989. doi: 10.1080/15513815.2023.2261043. Epub 2023 Nov 22. Fetal Pediatr Pathol. 2023. PMID: 37747279
Development of a novel method for amniotic fluid stem cell storage.
Zavatti M, Beretti F, Casciaro F, Comitini G, Franchi F, Barbieri V, Bertoni L, De Pol A, La Sala GB, Maraldi T. Zavatti M, et al. Among authors: barbieri v. Cytotherapy. 2017 Aug;19(8):1002-1012. doi: 10.1016/j.jcyt.2017.04.006. Epub 2017 May 29. Cytotherapy. 2017. PMID: 28571656 Free article.
Endocrinological Abnormalities Are a Main Feature of 17p13.1 Microduplication Syndrome: A New Case and Literature Review.
Maini I, Ivanovski I, Iodice A, Rosato S, Pollazzon M, Mussini M, Belligni EF, Coutton C, Marinelli M, Barbieri V, Napoli M, Pascarella R, Sartori C, Madia F, Fusco C, Franchi F, Street ME, Garavelli L. Maini I, et al. Among authors: barbieri v. Mol Syndromol. 2016 Nov;7(6):337-343. doi: 10.1159/000450718. Epub 2016 Oct 14. Mol Syndromol. 2016. PMID: 27920637 Free PMC article.