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Page 1
Galectin-3: One Molecule for an Alphabet of Diseases, from A to Z.
Int J Mol Sci. 2018 Jan 26;19(2):379. doi: 10.3390/ijms19020379.
Int J Mol Sci. 2018.
PMID: 29373564
Free PMC article.
Review.
Thyroid hormones regulate cardiac repolarization and QT-interval related gene expression in hiPSC cardiomyocytes.
Ulivieri A, Lavra L, Magi F, Morgante A, Calò L, Polisca P, Salehi LB, Sciacchitano S.
Ulivieri A, et al. Among authors: morgante a.
Sci Rep. 2022 Jan 12;12(1):568. doi: 10.1038/s41598-021-04659-w.
Sci Rep. 2022.
PMID: 35022468
Free PMC article.
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Retrospective analysis of seroprevalence in a cohort of university students of Rome (Italy) between September 2020 and July 2021.
Ulivieri A, Morgante A, Magi F, Salehi LB, Lavra L.
Ulivieri A, et al. Among authors: morgante a.
Epidemiol Prev. 2022 Sep-Dec;46(5-6):367-375. doi: 10.19191/EP22.5-6.A461.088.
Epidemiol Prev. 2022.
PMID: 36628641
English.
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Generation and characterization of the human induced pluripotent stem cell (hiPSC) line NCUFi001-A from a patient carrying KCNQ1 G314S mutation.
Lavra L, Magi F, Ulivieri A, Morgante A, Paulis M, Sala L, Pedrazzini M, Polisca P, Rocchetti M, Calò L, Sciacchitano S, Salehi LB.
Lavra L, et al. Among authors: morgante a.
Stem Cell Res. 2021 Jul;54:102418. doi: 10.1016/j.scr.2021.102418. Epub 2021 Jun 5.
Stem Cell Res. 2021.
PMID: 34130155
Free article.
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Nonthyroidal illness syndrome (NTIS) in severe COVID-19 patients: role of T3 on the Na/K pump gene expression and on hydroelectrolytic equilibrium.
Sciacchitano S, Capalbo C, Napoli C, Negro A, De Biase L, Marcolongo A, Anibaldi P, Salvati V, Petrella L, Merlo L, Alampi D, Alessandri E, Loffredo C, Ulivieri A, Lavra L, Magi F, Morgante A, Salehi LB, De Vitis C, Mancini R, Coluzzi F, Rocco M.
Sciacchitano S, et al. Among authors: morgante a.
J Transl Med. 2021 Dec 3;19(1):491. doi: 10.1186/s12967-021-03163-z.
J Transl Med. 2021.
PMID: 34861865
Free PMC article.
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Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2).
Catalli C, Morgante A, Iraci R, Rinaldi F, Botta A, Novelli G.
Catalli C, et al. Among authors: morgante a.
J Mol Diagn. 2010 Sep;12(5):601-6. doi: 10.2353/jmoldx.2010.090239. Epub 2010 Jul 8.
J Mol Diagn. 2010.
PMID: 20616365
Free PMC article.
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Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2.
Cardani R, Giagnacovo M, Botta A, Rinaldi F, Morgante A, Udd B, Raheem O, Penttilä S, Suominen T, Renna LV, Sansone V, Bugiardini E, Novelli G, Meola G.
Cardani R, et al. Among authors: morgante a.
J Neurol. 2012 Oct;259(10):2090-9. doi: 10.1007/s00415-012-6462-1. Epub 2012 Mar 10.
J Neurol. 2012.
PMID: 22407275
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