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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1992 1
1995 2
1996 1
1997 1
2012 1
2013 1
2014 1
2015 3
2016 2
2018 4
2019 3
2020 4
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22 results
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Page 1
Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art Review.
Arbustini E, Di Toro A, Giuliani L, Favalli V, Narula N, Grasso M. Arbustini E, et al. Among authors: di toro a. J Am Coll Cardiol. 2018 Nov 13;72(20):2485-2506. doi: 10.1016/j.jacc.2018.08.2182. J Am Coll Cardiol. 2018. PMID: 30442292 Free article. Review.
Anderson-Fabry disease.
Di Toro A, Favalli V, Arbustini E. Di Toro A, et al. J Cardiovasc Med (Hagerstown). 2018 Feb;19 Suppl 1:e1-e5. doi: 10.2459/JCM.0000000000000637. J Cardiovasc Med (Hagerstown). 2018. PMID: 29538136 Review. No abstract available.
When Genes, More Than Phenotype, Identify Different Diseases: The Case of Nonsyndromic HTAA/D.
Arbustini E, Giuliani L, Di Toro A. Arbustini E, et al. Among authors: di toro a. J Am Coll Cardiol. 2018 Aug 7;72(6):616-619. doi: 10.1016/j.jacc.2018.03.547. J Am Coll Cardiol. 2018. PMID: 30071990 Free article. No abstract available.
Common presentation of rare diseases: Aortic aneurysms & valves.
Arbustini E, Favalli V, Di Toro A, Giuliani L, Limongelli G. Arbustini E, et al. Among authors: di toro a. Int J Cardiol. 2018 Apr 15;257:358-365. doi: 10.1016/j.ijcard.2018.01.003. Int J Cardiol. 2018. PMID: 29506732 Review.
Diagnostic role of head-up tilt test in patients with cough syncope.
Mereu R, Taraborrelli P, Sau A, Di Toro A, Halim S, Hayat S, Bernardi L, Francis DP, Sutton R, Lim PB. Mereu R, et al. Among authors: di toro a. Europace. 2016 Aug;18(8):1273-9. doi: 10.1093/europace/euv283. Epub 2016 Jan 18. Europace. 2016. PMID: 26787669 Free PMC article.
Diagnostic Criteria of Left Ventricular Dysfunction in Patients With Myotonic Dystrophy Type 1.
Di Toro A, Giuliani L, Serio A, Arbustini E. Di Toro A, et al. J Card Fail. 2020 Oct;26(10):857-859. doi: 10.1016/j.cardfail.2019.09.016. Epub 2019 Oct 8. J Card Fail. 2020. PMID: 31604117 No abstract available.
Genetics and clinics: current applications, limitations, and future developments.
Di Toro A, Giuliani L, Favalli V, Di Giovannantonio M, Smirnova A, Grasso M, Arbustini E. Di Toro A, et al. Eur Heart J Suppl. 2019 Mar;21(Suppl B):B7-B14. doi: 10.1093/eurheartj/suz048. Epub 2019 Mar 29. Eur Heart J Suppl. 2019. PMID: 30948934 Free PMC article. No abstract available.
Prenatal diagnosis of Fraser syndrome: a matter of life or death?
De Bernardo G, Giordano M, Di Toro A, Sordino D, De Brasi D. De Bernardo G, et al. Among authors: di toro a. Ital J Pediatr. 2015 Nov 9;41:86. doi: 10.1186/s13052-015-0195-6. Ital J Pediatr. 2015. PMID: 26552811 Free PMC article.
Ceftazidine-avibactam salvage therapy in newborn with KPC-producing Klebsiella pneumoniae invasive infections.
Esposito P, Sbrana F, Di Toro A, Gombos S, Tascini C. Esposito P, et al. Among authors: di toro a. Minerva Anestesiol. 2019 Jul;85(7):804-805. doi: 10.23736/S0375-9393.19.13521-3. Minerva Anestesiol. 2019. PMID: 31271023 Free article. No abstract available.
Renal and brain complications in GLA p.Phe113Leu Fabry disease. Comments on "Fabry disease caused by the GLA p.Phe113Leu (p.F113L) variant: Natural history in males" by Oliveira et al. (Eur. J. Med. Genet. 2019).
Smirnova A, Di Toro A, Giuliani L, Tagliani M, Urtis M, Favalli V, Arbustini E. Smirnova A, et al. Among authors: di toro a. Eur J Med Genet. 2020 Apr;63(4):103847. doi: 10.1016/j.ejmg.2020.103847. Epub 2020 Jan 13. Eur J Med Genet. 2020. PMID: 31945513 No abstract available.
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