Accadia M[Author] - Search Results

Year	Number of Results
1989	1
1993	1
1995	1
1999	2
2002	2
2003	2
2004	5
2005	1
2006	4
2007	2
2008	5
2009	2
2011	1
2012	1
2017	3
2018	3
2019	4
2020	2
2021	2

1

Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome.

Pannone L, Bocchinfuso G, Flex E, Rossi C, Baldassarre G, Lissewski C, Pantaleoni F, Consoli F, Lepri F, Magliozzi M, Anselmi M, Delle Vigne S, Sorge G, Karaer K, Cuturilo G, Sartorio A, Tinschert S, Accadia M, Digilio MC, Zampino G, De Luca A, Cavé H, Zenker M, Gelb BD, Dallapiccola B, Stella L, Ferrero GB, Martinelli S, Tartaglia M. Pannone L, et al. Among authors: accadia m. Hum Mutat. 2017 Apr;38(4):451-459. doi: 10.1002/humu.23175. Epub 2017 Feb 7. Hum Mutat. 2017. PMID: 28074573

2

Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus.

Maggiolini FAM, Cantsilieris S, D'Addabbo P, Manganelli M, Coe BP, Dumont BL, Sanders AD, Pang AWC, Vollger MR, Palumbo O, Palumbo P, Accadia M, Carella M, Eichler EE, Antonacci F. Maggiolini FAM, et al. Among authors: accadia m. PLoS Genet. 2019 Mar 27;15(3):e1008075. doi: 10.1371/journal.pgen.1008075. eCollection 2019 Mar. PLoS Genet. 2019. PMID: 30917130 Free PMC article.

3

Pericardial thrombus and cardiac tamponade after pericardiocentesis with intact heart walls.

Accadia M, Di Maio M, Iengo R, Arnese M, Cocchia R, Scotto Di Uccio F, Tuccillo A, Mercogliano G, Tuccillo B. Accadia M, et al. Echocardiography. 2019 Apr;36(4):803-805. doi: 10.1111/echo.14276. Epub 2019 Feb 6. Echocardiography. 2019. PMID: 30726561

4

Customised next-generation sequencing multigene panel to screen a large cohort of individuals with chromatin-related disorder.

Squeo GM, Augello B, Massa V, Milani D, Colombo EA, Mazza T, Castellana S, Piccione M, Maitz S, Petracca A, Prontera P, Accadia M, Della Monica M, Di Giacomo MC, Melis D, Selicorni A, Giglio S, Fischetto R, Di Fede E, Malerba N, Russo M, Castori M, Gervasini C, Merla G. Squeo GM, et al. Among authors: accadia m. J Med Genet. 2020 Nov;57(11):760-768. doi: 10.1136/jmedgenet-2019-106724. Epub 2020 Mar 13. J Med Genet. 2020. PMID: 32170002

5

Correction to: Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation.

Capozza M, Chinellato I, Guarnieri V, Di Iorgi N, Accadia M, Traggiai C, Mattioli G, Di Mauro A, Laforgia N. Capozza M, et al. Among authors: accadia m. BMC Pediatr. 2019 Nov 27;19(1):463. doi: 10.1186/s12887-019-1850-7. BMC Pediatr. 2019. PMID: 31771548 Free PMC article.

6

Epicardial Adipose Tissue and IL-13 Response to Myocardial Injury Drives Left Ventricular Remodeling After ST Elevation Myocardial Infarction.

Parisi V, Cabaro S, D'Esposito V, Petraglia L, Conte M, Campana P, Gerundo G, Abitabile M, Tuccillo A, Accadia M, Comentale G, Pilato E, Sansone M, Leosco D, Formisano P. Parisi V, et al. Among authors: accadia m. Front Physiol. 2020 Oct 15;11:575181. doi: 10.3389/fphys.2020.575181. eCollection 2020. Front Physiol. 2020. PMID: 33178043 Free PMC article.

7

Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription.

Di Stolfo G, Accadia M, Mastroianno S, Leone MP, Palumbo O, Palumbo P, Potenza D, Maccarone P, Sacco M, Russo A, Carella M. Di Stolfo G, et al. Among authors: accadia m. Mol Genet Genomic Med. 2019 Sep;7(9):e855. doi: 10.1002/mgg3.855. Epub 2019 Jul 25. Mol Genet Genomic Med. 2019. PMID: 31347270 Free PMC article.

8

Genetic imprinting: the paradigm of Prader-Willi and Angelman syndromes.

Gurrieri F, Accadia M. Gurrieri F, et al. Among authors: accadia m. Endocr Dev. 2009;14:20-8. doi: 10.1159/000207473. Epub 2009 Feb 27. Endocr Dev. 2009. PMID: 19293572 Review.

9

Case report: acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation.

Capozza M, Chinellato I, Guarnieri V, Di Lorgi N, Accadia M, Traggiai C, Mattioli G, Di Mauro A, Laforgia N. Capozza M, et al. Among authors: accadia m. BMC Pediatr. 2018 Oct 30;18(1):340. doi: 10.1186/s12887-018-1319-0. BMC Pediatr. 2018. PMID: 30376845 Free PMC article.

10

Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome.

Palumbo P, Accadia M, Leone MP, Palladino T, Stallone R, Carella M, Palumbo O. Palumbo P, et al. Among authors: accadia m. Am J Med Genet A. 2018 Feb;176(2):391-398. doi: 10.1002/ajmg.a.38559. Epub 2017 Nov 28. Am J Med Genet A. 2018. PMID: 29193617

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