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

Year Number of Results
1995 1
1998 1
2003 1
2008 1
2010 1
2011 1
2012 1
2014 1
2016 2
2017 4
2018 1
2020 3
2023 1
2024 0

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16 results

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Page 1
Cardiac involvement in Lysosomal Storage Diseases.
Sestito S, Parisi F, Tallarico V, Tarsitano F, Roppa K, Pensabene L, Chimenz R, Ceravolo G, Calabrò MP, De Sarro R, Moricca MT, Bonapace G, Concolino D. Sestito S, et al. Among authors: moricca mt. J Biol Regul Homeost Agents. 2020 Jul-Aug;34(4 Suppl. 2):107-119. SPECIAL ISSUE: FOCUS ON PEDIATRIC CARDIOLOGY. J Biol Regul Homeost Agents. 2020. PMID: 33000609 Review.
Genetics and Gene Therapy in Hunter Disease.
Sestito S, Falvo F, Scozzafava C, Apa R, Pensabene L, Bonapace G, Moricca MT, Concolino D. Sestito S, et al. Among authors: moricca mt. Curr Gene Ther. 2018;18(2):90-95. doi: 10.2174/1566523218666180404155759. Curr Gene Ther. 2018. PMID: 29618310 Review.
The heart in Anderson-Fabry disease.
Sestito S, Roppa K, Parisi F, Moricca MT, Pensabene L, Chimenz R, Ceravolo MD, Cucinotta U, Ceravolo G, Calabrò MP, Cuppari C, Mondello P, Musolino D, Tallarico V, Concolino D. Sestito S, et al. Among authors: moricca mt. J Biol Regul Homeost Agents. 2020 Jul-Aug;34(4 Suppl. 2):63-69. SPECIAL ISSUE: FOCUS ON PEDIATRIC CARDIOLOGY. J Biol Regul Homeost Agents. 2020. PMID: 33000603 No abstract available.
Dilated cardiomyopathy in mucolipidosis type 2.
Carboni E, Sestito S, Lucente M, Morrone A, Zampini L, Chimenz R, Ceravolo MD, De Sarro R, Ceravolo G, Calabrò MP, Parisi F, Moricca MT, Pensabene L, Musolino D, Concolino D. Carboni E, et al. Among authors: moricca mt. J Biol Regul Homeost Agents. 2020 Jul-Aug;34(4 Suppl. 2):71-77. SPECIAL ISSUE: FOCUS ON PEDIATRIC CARDIOLOGY. J Biol Regul Homeost Agents. 2020. PMID: 33000604
c.376A>G, (p.Ser126Gly) Alpha-Galactosidase A mutation induces ER stress, unfolded protein response and reduced enzyme trafficking to lysosome: Possible relevance in the pathogenesis of late-onset forms of Fabry Disease.
Riillo C, Bonapace G, Moricca MT, Sestito S, Salatino A, Concolino D. Riillo C, et al. Among authors: moricca mt. Mol Genet Metab. 2023 Nov;140(3):107700. doi: 10.1016/j.ymgme.2023.107700. Epub 2023 Sep 14. Mol Genet Metab. 2023. PMID: 37774431 Free article.
Partial trisomy 1(q42-->qter): a new case with a mild phenotype.
Concolino D, Cinti R, Ferraro L, Moricca MT, Strisciuglio P. Concolino D, et al. Among authors: moricca mt. J Med Genet. 1998 Jan;35(1):75-7. doi: 10.1136/jmg.35.1.75. J Med Genet. 1998. PMID: 9475102 Free PMC article. Review.
Norrbottnian clinical variant of Gaucher disease in Southern Italy.
Sestito S, Filocamo M, Ceravolo F, Falvo F, Grisolia M, Moricca MT, Cantaffa R, Grossi S, Strisciuglio P, Concolino D. Sestito S, et al. Among authors: moricca mt. J Hum Genet. 2017 Apr;62(4):507-511. doi: 10.1038/jhg.2016.158. Epub 2016 Dec 22. J Hum Genet. 2017. PMID: 28003644
16 results