Ergoli M - Search Results

1

X-Linked Emery-Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female Carriers.

Viggiano E, Madej-Pilarczyk A, Carboni N, Picillo E, Ergoli M, Gaudio SD, Marchel M, Nigro G, Palladino A, Politano L. Viggiano E, et al. Among authors: ergoli m. Genes (Basel). 2019 Nov 11;10(11):919. doi: 10.3390/genes10110919. Genes (Basel). 2019. PMID: 31718017 Free PMC article.

2

Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy.

Viggiano E, Ergoli M, Picillo E, Politano L. Viggiano E, et al. Among authors: ergoli m. Hum Genet. 2016 Jul;135(7):685-98. doi: 10.1007/s00439-016-1666-6. Epub 2016 Apr 21. Hum Genet. 2016. PMID: 27098336 Review.

3

Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy.

Viggiano E, Picillo E, Ergoli M, Cirillo A, Del Gaudio S, Politano L. Viggiano E, et al. Among authors: ergoli m. J Gene Med. 2017 Apr;19(4). doi: 10.1002/jgm.2952. J Gene Med. 2017. PMID: 28316128

4

Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene.

Taglia A, Petillo R, D'Ambrosio P, Picillo E, Torella A, Orsini C, Ergoli M, Scutifero M, Passamano L, Palladino A, Nigro G, Politano L. Taglia A, et al. Among authors: ergoli m. Acta Myol. 2015 May;34(1):9-13. Acta Myol. 2015. PMID: 26155064 Free PMC article.

5

Novel mutations in LMNA A/C gene and associated phenotypes.

Petillo R, D'Ambrosio P, Torella A, Taglia A, Picillo E, Testori A, Ergoli M, Nigro G, Piluso G, Nigro V, Politano L. Petillo R, et al. Among authors: ergoli m. Acta Myol. 2015 Dec;34(2-3):116-9. Acta Myol. 2015. PMID: 27199538 Free PMC article.

6

Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results.

Palladino A, Papa AA, Morra S, Russo V, Ergoli M, Rago A, Orsini C, Nigro G, Politano L. Palladino A, et al. Among authors: ergoli m. Acta Myol. 2019 Mar 1;38(1):1-7. eCollection 2019 Mar. Acta Myol. 2019. PMID: 31309174 Free PMC article. Review.

7

Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies.

D'Ambrosio P, Petillo R, Torella A, Papa AA, Palladino A, Orsini C, Ergoli M, Passamano L, Novelli A, Nigro V, Politano L. D'Ambrosio P, et al. Among authors: ergoli m. Acta Myol. 2019 Jun 1;38(2):33-36. eCollection 2019 Jun. Acta Myol. 2019. PMID: 31309180 Free PMC article.

8

Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function.

Ergoli M, Venditti M, Picillo E, Minucci S, Politano L. Ergoli M, et al. Mol Reprod Dev. 2020 Jan;87(1):45-52. doi: 10.1002/mrd.23307. Epub 2019 Dec 16. Mol Reprod Dev. 2020. PMID: 31840338

9

Study of anti-Müllerian hormone levels in patients with Myotonic Dystrophy Type 1. Preliminary results.

Ergoli M, Venditti M, Dotolo R, Picillo E, Minucci S, Politano L. Ergoli M, et al. Acta Myol. 2017 Dec 1;36(4):199-202. eCollection 2017 Dec. Acta Myol. 2017. PMID: 29770362 Free PMC article.

10

Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy.

Spitali P, Hettne K, Tsonaka R, Sabir E, Seyer A, Hemerik JBA, Goeman JJ, Picillo E, Ergoli M, Politano L, Aartsma-Rus A. Spitali P, et al. Among authors: ergoli m. J Cell Mol Med. 2018 Apr;22(4):2442-2448. doi: 10.1111/jcmm.13543. Epub 2018 Feb 14. J Cell Mol Med. 2018. PMID: 29441734 Free PMC article.

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