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

Year Number of Results
1965 1
1971 1
1976 1
1982 1
1983 2
1985 1
1986 1
1987 1
1989 2
1990 3
1991 2
1992 7
1993 4
1994 2
1995 1
1996 4
1997 4
1998 5
1999 3
2000 5
2001 5
2003 3
2004 3
2006 1
2007 2
2008 2
2009 1
2010 4
2011 3
2012 6
2013 4
2014 4
2015 6
2016 1
2018 4
2019 2
2020 2
2022 1
2024 0

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99 results

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Page 1
Recommendations for the predictive genetic test in Huntington's disease.
MacLeod R, Tibben A, Frontali M, Evers-Kiebooms G, Jones A, Martinez-Descales A, Roos RA; Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network. MacLeod R, et al. Among authors: frontali m. Clin Genet. 2013 Mar;83(3):221-31. doi: 10.1111/j.1399-0004.2012.01900.x. Epub 2012 Jul 30. Clin Genet. 2013. PMID: 22642570 No abstract available.
Episodic Ataxias: Faux or Real?
Giunti P, Mantuano E, Frontali M. Giunti P, et al. Among authors: frontali m. Int J Mol Sci. 2020 Sep 5;21(18):6472. doi: 10.3390/ijms21186472. Int J Mol Sci. 2020. PMID: 32899446 Free PMC article. Review.
Diagnostic genetic testing for Huntington's disease.
Craufurd D, MacLeod R, Frontali M, Quarrell O, Bijlsma EK, Davis M, Hjermind LE, Lahiri N, Mandich P, Martinez A, Tibben A, Roos RA; Working Group on Genetic Counselling and Testing of the European Huntington's Disease Network (EHDN). Craufurd D, et al. Among authors: frontali m. Pract Neurol. 2015 Feb;15(1):80-4. doi: 10.1136/practneurol-2013-000790. Epub 2014 Aug 28. Pract Neurol. 2015. PMID: 25169240 Review. No abstract available.
EMQN Best Practice Guidelines for molecular genetic testing of SCAs.
Sequeiros J, Martindale J, Seneca S, Giunti P, Kämäräinen O, Volpini V, Weirich H, Christodoulou K, Bazak N, Sinke R, Sulek-Piatkowska A, Garcia-Planells J, Davis M, Frontali M, Hämäläinen P, Wieczorek S, Zühlke C, Saraiva-Pereira ML, Warner J, Leguern E, Thonney F, Quintáns Castro B, Jonasson J, Storm K, Andersson A, Ravani A, Correia L, Silveira I, Alonso I, Martins C, Pinto Basto J, Coutinho P, Perdigão A, Barton D, Davis M; European Molecular Quality Genetics Network. Sequeiros J, et al. Among authors: frontali m. Eur J Hum Genet. 2010 Nov;18(11):1173-6. doi: 10.1038/ejhg.2010.8. Epub 2010 Feb 24. Eur J Hum Genet. 2010. PMID: 20179742 Free PMC article.
"Microcytogenetics" and Langer-Giedion syndrome.
Frontali M, Ramenghi M, Trabace S, Dallapiccola B. Frontali M, et al. J Med Genet. 1982 Oct;19(5):390-1. doi: 10.1136/jmg.19.5.390-a. J Med Genet. 1982. PMID: 7143397 Free PMC article. No abstract available.
Leukocyte telomere shortening in Huntington's disease.
Scarabino D, Veneziano L, Peconi M, Frontali M, Mantuano E, Corbo RM. Scarabino D, et al. Among authors: frontali m. J Neurol Sci. 2019 Jan 15;396:25-29. doi: 10.1016/j.jns.2018.10.024. Epub 2018 Oct 28. J Neurol Sci. 2019. PMID: 30396032
Another patient with 12q13 microduplication.
Bertoli M, Alesi V, Gullotta F, Zampatti S, Abate MR, Palmieri C, Novelli A, Frontali M, Nardone AM. Bertoli M, et al. Among authors: frontali m. Am J Med Genet A. 2013 Aug;161A(8):2004-8. doi: 10.1002/ajmg.a.35991. Epub 2013 Jul 3. Am J Med Genet A. 2013. PMID: 23824684
99 results