Scutifero M - Search Results

1

Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.

Pizza A, Picillo E, Onore ME, Scutifero M, Passamano L, Nigro V, Politano L. Pizza A, et al. Among authors: scutifero m. Acta Myol. 2023 Mar 31;42(1):24-30. doi: 10.36185/2532-1900-246. eCollection 2023. Acta Myol. 2023. PMID: 37091526 Free PMC article. Review.

2

Cardiac involvement in patients with spinal muscular atrophies.

Palladino A, Passamano L, Taglia A, D'Ambrosio P, Scutifero M, Cecio MR, Picillo E, Viggiano E, Torre V, De Luca F, Nigro G, Politano L. Palladino A, et al. Among authors: scutifero m. Acta Myol. 2011 Dec;30(3):175-8. Acta Myol. 2011. PMID: 22616198 Free PMC article.

3

Improvement of survival in Duchenne Muscular Dystrophy: retrospective analysis of 835 patients.

Passamano L, Taglia A, Palladino A, Viggiano E, D'Ambrosio P, Scutifero M, Rosaria Cecio M, Torre V, DE Luca F, Picillo E, Paciello O, Piluso G, Nigro G, Politano L. Passamano L, et al. Among authors: scutifero m. Acta Myol. 2012 Oct;31(2):121-5. Acta Myol. 2012. PMID: 23097603 Free PMC article.

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: scutifero m. Acta Myol. 2015 May;34(1):9-13. Acta Myol. 2015. PMID: 26155064 Free PMC article.

5

Management of cardiac involvement in muscular dystrophies: paediatric versus adult forms.

Palladino A, D'Ambrosio P, Papa AA, Petillo R, Orsini C, Scutifero M, Nigro G, Politano L. Palladino A, et al. Among authors: scutifero m. Acta Myol. 2016 Dec;35(3):128-134. Acta Myol. 2016. PMID: 28484313 Free PMC article. Review.

6

Can symptomatic nmDuchenne carriers benefit from treatment with ataluren? Results of 193-month follow-up.

Dori A, Guglieri M, Scutifero M, Passamano L, Trabacca A, Politano L. Dori A, et al. Among authors: scutifero m. Acta Myol. 2021 Dec 31;40(4):152-157. doi: 10.36185/2532-1900-058. eCollection 2021 Dec. Acta Myol. 2021. PMID: 35047755 Free PMC article. Retracted.

7

Gender effect on onset, prevalence and surgical treatment of cataract in patients with Myotonic Dystrophy type 1.

Scutifero M, Lanza M, Petillo R, De Bernardo M, Passamano L, Rosa N, Politano L. Scutifero M, et al. Acta Myol. 2022 Sep 30;41(3):105-110. doi: 10.36185/2532-1900-N75. eCollection 2022. Acta Myol. 2022. PMID: 36349183 Free PMC article.

8

Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy.

Viggiano E, Picillo E, Passamano L, Onore ME, Piluso G, Scutifero M, Torella A, Nigro V, Politano L. Viggiano E, et al. Among authors: scutifero m. Genes (Basel). 2023 Jan 14;14(1):214. doi: 10.3390/genes14010214. Genes (Basel). 2023. PMID: 36672955 Free PMC article.

9

Usefulness of heart rate variability as a predictor of sudden cardiac death in muscular dystrophies.

Politano L, Palladino A, Nigro G, Scutifero M, Cozza V. Politano L, et al. Among authors: scutifero m. Acta Myol. 2008 Dec;27(3):114-22. Acta Myol. 2008. PMID: 19472920 Free PMC article. Review.

10

Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study.

Magliano L, D'Angelo MG, Vita G, Pane M, D'Amico A, Balottin U, Angelini C, Battini R, Politano L, Patalano M, Sagliocchi A, Civati F, Brighina E, Vita GL, Messina S, Sframeli M, Lombardo ME, Scalise R, Colia G, Catteruccia M, Berardinelli A, Motta MC, Gaiani A, Semplicini C, Bello L, Astrea G, Zaccaro A, Scutifero M. Magliano L, et al. Among authors: scutifero m. Acta Myol. 2014 Dec;33(3):136-43. Acta Myol. 2014. PMID: 25873782 Free PMC article.

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