Frisso G - Search Results

1

Molecular Epidemiology of Mitochondrial Cardiomyopathy: A Search Among Mitochondrial and Nuclear Genes.

Mazzaccara C, Mirra B, Barretta F, Caiazza M, Lombardo B, Scudiero O, Tinto N, Limongelli G, Frisso G. Mazzaccara C, et al. Among authors: frisso g. Int J Mol Sci. 2021 May 27;22(11):5742. doi: 10.3390/ijms22115742. Int J Mol Sci. 2021. PMID: 34072184 Free PMC article. Review.

2

Direct detection of exon deletions/duplications in female carriers of and male patients with Duchenne/Becker muscular dystrophy.

Frisso G, Carsana A, Tinto N, Calcagno G, Salvatore F, Sacchetti L. Frisso G, et al. Clin Chem. 2004 Aug;50(8):1435-8. doi: 10.1373/clinchem.2004.033795. Clin Chem. 2004. PMID: 15277355 Free article. No abstract available.

3

A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy.

Frisso G, Limongelli G, Pacileo G, Del Giudice A, Forgione L, Calabrò P, Iacomino M, Detta N, Di Fonzo LM, Maddaloni V, Calabrò R, Salvatore F. Frisso G, et al. Clin Genet. 2009 Jul;76(1):91-101. doi: 10.1111/j.1399-0004.2009.01190.x. Clin Genet. 2009. PMID: 19659763

4

DNA sequence capture and next-generation sequencing for the molecular diagnosis of genetic cardiomyopathies.

D'Argenio V, Frisso G, Precone V, Boccia A, Fienga A, Pacileo G, Limongelli G, Paolella G, Calabrò R, Salvatore F. D'Argenio V, et al. Among authors: frisso g. J Mol Diagn. 2014 Jan;16(1):32-44. doi: 10.1016/j.jmoldx.2013.07.008. Epub 2013 Oct 31. J Mol Diagn. 2014. PMID: 24183960 Free article.

5

Genetic analysis in a family affected by sick sinus syndrome may reduce the sudden death risk in a young aspiring competitive athlete.

Detta N, Frisso G, Limongelli G, Marzullo M, Calabrò R, Salvatore F. Detta N, et al. Among authors: frisso g. Int J Cardiol. 2014 Jan 1;170(3):e63-5. doi: 10.1016/j.ijcard.2013.11.013. Epub 2013 Nov 12. Int J Cardiol. 2014. PMID: 24295898 Free article. No abstract available.

6

Significance of sarcomere gene mutations analysis in the end-stage phase of hypertrophic cardiomyopathy.

Biagini E, Olivotto I, Iascone M, Parodi MI, Girolami F, Frisso G, Autore C, Limongelli G, Cecconi M, Maron BJ, Maron MS, Rosmini S, Formisano F, Musumeci B, Cecchi F, Iacovoni A, Haas TS, Bacchi Reggiani ML, Ferrazzi P, Salvatore F, Spirito P, Rapezzi C. Biagini E, et al. Among authors: frisso g. Am J Cardiol. 2014 Sep 1;114(5):769-76. doi: 10.1016/j.amjcard.2014.05.065. Epub 2014 Jun 19. Am J Cardiol. 2014. PMID: 25037680

7

Clinical and genetic characterization of patients with hypertrophic cardiomyopathy and right atrial enlargement.

Limongelli G, Masarone D, Frisso G, Iacomino M, Ferrara I, Rea A, Gravino R, Bossone E, Salvatore F, Calabro R, Elliott P, Pacileo G. Limongelli G, et al. Among authors: frisso g. J Cardiovasc Med (Hagerstown). 2017 Apr;18(4):249-254. doi: 10.2459/JCM.0000000000000361. J Cardiovasc Med (Hagerstown). 2017. PMID: 26808413

8

Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing.

Mozzillo E, Cozzolino C, Genesio R, Melis D, Frisso G, Orrico A, Lombardo B, Fattorusso V, Discepolo V, Della Casa R, Simonelli F, Nitsch L, Salvatore F, Franzese A. Mozzillo E, et al. Among authors: frisso g. Am J Med Genet A. 2016 Aug;170(8):2196-9. doi: 10.1002/ajmg.a.37770. Epub 2016 Jun 3. Am J Med Genet A. 2016. PMID: 27256967

9

Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies.

Frisso G, Detta N, Coppola P, Mazzaccara C, Pricolo MR, D'Onofrio A, Limongelli G, Calabrò R, Salvatore F. Frisso G, et al. Int J Mol Sci. 2016 Nov 10;17(11):1883. doi: 10.3390/ijms17111883. Int J Mol Sci. 2016. PMID: 27834932 Free PMC article.

10

Successful Pregnancy in a Young Woman with Multiple Acyl-CoA Dehydrogenase Deficiency.

Creanza A, Cotugno M, Mazzaccara C, Frisso G, Parenti G, Capaldo B. Creanza A, et al. Among authors: frisso g. JIMD Rep. 2018;39:1-6. doi: 10.1007/8904_2017_38. Epub 2017 Jul 7. JIMD Rep. 2018. PMID: 28685490 Free PMC article.

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