Girolami F - Search Results

1

Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations.

Girolami F, Ho CY, Semsarian C, Baldi M, Will ML, Baldini K, Torricelli F, Yeates L, Cecchi F, Ackerman MJ, Olivotto I. Girolami F, et al. J Am Coll Cardiol. 2010 Apr 6;55(14):1444-53. doi: 10.1016/j.jacc.2009.11.062. J Am Coll Cardiol. 2010. PMID: 20359594 Free article.

2

Hereditary Thoracic Aortic Diseases.

Spaziani G, Surace FC, Girolami F, Bianco F, Bucciarelli V, Bonanni F, Bennati E, Arcieri L, Favilli S. Spaziani G, et al. Among authors: girolami f. Diagnostics (Basel). 2024 Jan 4;14(1):112. doi: 10.3390/diagnostics14010112. Diagnostics (Basel). 2024. PMID: 38201421 Free PMC article. Review.

3

Identification of seven novel mutations of F8C by DHPLC.

Frusconi S, Passerini I, Girolami F, Masieri M, Linari S, Longo G, Morfini M, Torricelli F. Frusconi S, et al. Among authors: girolami f. Hum Mutat. 2002 Sep;20(3):231-2. doi: 10.1002/humu.9052. Hum Mutat. 2002. PMID: 12203998

4

Microsatellite analysis of chromosome 3p region in sporadic renal cell carcinomas.

Girolami F, Passerini I, Gargano D, Frusconi S, Villari D, Nicita G, Torricelli F. Girolami F, et al. Pathol Oncol Res. 2002;8(4):241-4. doi: 10.1007/BF03036738. Epub 2003 Feb 11. Pathol Oncol Res. 2002. PMID: 12579209 Free article.

5

Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany.

Torricelli F, Girolami F, Olivotto I, Passerini I, Frusconi S, Vargiu D, Richard P, Cecchi F. Torricelli F, et al. Among authors: girolami f. Am J Cardiol. 2003 Dec 1;92(11):1358-62. doi: 10.1016/j.amjcard.2003.08.031. Am J Cardiol. 2003. PMID: 14636924

6

Relevance of coronary microvascular flow impairment to long-term remodeling and systolic dysfunction in hypertrophic cardiomyopathy.

Olivotto I, Cecchi F, Gistri R, Lorenzoni R, Chiriatti G, Girolami F, Torricelli F, Camici PG. Olivotto I, et al. Among authors: girolami f. J Am Coll Cardiol. 2006 Mar 7;47(5):1043-8. doi: 10.1016/j.jacc.2005.10.050. J Am Coll Cardiol. 2006. PMID: 16516091 Free article.

7

A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.

Girolami F, Olivotto I, Passerini I, Zachara E, Nistri S, Re F, Fantini S, Baldini K, Torricelli F, Cecchi F. Girolami F, et al. J Cardiovasc Med (Hagerstown). 2006 Aug;7(8):601-7. doi: 10.2459/01.JCM.0000237908.26377.d6. J Cardiovasc Med (Hagerstown). 2006. PMID: 16858239

8

Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy.

Olivotto I, Girolami F, Ackerman MJ, Nistri S, Bos JM, Zachara E, Ommen SR, Theis JL, Vaubel RA, Re F, Armentano C, Poggesi C, Torricelli F, Cecchi F. Olivotto I, et al. Among authors: girolami f. Mayo Clin Proc. 2008 Jun;83(6):630-8. doi: 10.4065/83.6.630. Mayo Clin Proc. 2008. PMID: 18533079 Clinical Trial.

9

The familial hypertrophic cardiomyopathy-associated myosin mutation R403Q accelerates tension generation and relaxation of human cardiac myofibrils.

Belus A, Piroddi N, Scellini B, Tesi C, D'Amati G, Girolami F, Yacoub M, Cecchi F, Olivotto I, Poggesi C. Belus A, et al. Among authors: girolami f. J Physiol. 2008 Aug 1;586(15):3639-44. doi: 10.1113/jphysiol.2008.155952. Epub 2008 Jun 19. J Physiol. 2008. PMID: 18565996 Free PMC article.

10

[A new type of "tracing" for cardiologists?].

Baldi M, Girolami F. Baldi M, et al. Among authors: girolami f. G Ital Cardiol (Rome). 2009 Apr;10(4):266. G Ital Cardiol (Rome). 2009. PMID: 19475884 Italian. No abstract available.

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