Frisso G - Search Results

1

Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options.

Lioncino M, Monda E, Caiazza M, Fusco A, Cirillo A, Dongiglio F, Simonelli V, Sampaolo S, Ruggiero L, Scarano G, Pota V, Frisso G, Mazzaccara C, D'Amati G, Nigro G, Russo MG, Wahbi K, Limongelli G. Lioncino M, et al. Among authors: frisso g. Heart Fail Clin. 2022 Jan;18(1):51-60. doi: 10.1016/j.hfc.2021.07.003. Epub 2021 Oct 26. Heart Fail Clin. 2022. PMID: 34776083 Review.

2

Novel deletion at the M and P promoters of the human dystrophin gene associated with a Duchenne muscular dystrophy.

Frisso G, Sampaolo S, Pastore L, Carlomagno A, Calise RM, Di Iorio G, Salvatore F. Frisso G, et al. Neuromuscul Disord. 2002 Jun;12(5):494-7. doi: 10.1016/s0960-8966(01)00323-6. Neuromuscul Disord. 2002. PMID: 12031623

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

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.

9

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.

10

Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications.

Girolami F, Frisso G, Benelli M, Crotti L, Iascone M, Mango R, Mazzaccara C, Pilichou K, Arbustini E, Tomberli B, Limongelli G, Basso C, Olivotto I. Girolami F, et al. Among authors: frisso g. J Cardiovasc Med (Hagerstown). 2018 Jan;19(1):1-11. doi: 10.2459/JCM.0000000000000589. J Cardiovasc Med (Hagerstown). 2018. PMID: 29176389 Free PMC article.

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