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

Year Number of Results
1969 1
1971 1
1973 3
1976 2
1977 2
1978 1
1981 1
1982 1
1985 1
1986 1
1988 2
1989 3
1994 1
1996 1
1997 3
1998 1
1999 2
2000 5
2001 4
2002 1
2004 1
2005 2
2006 2
2007 2
2008 2
2010 1
2013 1
2014 1
2015 1
2024 0

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49 results

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Page 1
Genetic services in Italy.
Bricarelli FD, Dallapiccola B, Provedel R, Romeo G. Bricarelli FD, et al. Eur J Hum Genet. 1997;5 Suppl 2:112-5. Eur J Hum Genet. 1997. PMID: 9450206 No abstract available.
Lack of SCN1A mutations in familial febrile seizures.
Malacarne M, Madia F, Gennaro E, Vacca D, Güney AI, Buono S, Bernardina BD, Gaggero R, Gobbi G, Lispi ML, Malamaci D, Melideo G, Roccella M, Sferro C, Tiberti A, Vanadia F, Vigevano F, Viri F, Vitali MR, Bricarelli FD, Bianchi A, Zara F. Malacarne M, et al. Among authors: bricarelli fd. Epilepsia. 2002 May;43(5):559-62. doi: 10.1046/j.1528-1157.2002.29301.x. Epilepsia. 2002. PMID: 12027919 Free article.
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy.
Gennaro E, Santorelli FM, Bertini E, Buti D, Gaggero R, Gobbi G, Lini M, Granata T, Freri E, Parmeggiani A, Striano P, Veggiotti P, Cardinali S, Bricarelli FD, Minetti C, Zara F. Gennaro E, et al. Among authors: bricarelli fd. Biochem Biophys Res Commun. 2006 Mar 10;341(2):489-93. doi: 10.1016/j.bbrc.2005.12.209. Epub 2006 Jan 13. Biochem Biophys Res Commun. 2006. PMID: 16430863
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases.
Mora M, Angelini C, Bignami F, Bodin AM, Crimi M, Di Donato JH, Felice A, Jaeger C, Karcagi V, LeCam Y, Lynn S, Meznaric M, Moggio M, Monaco L, Politano L, de la Paz MP, Saker S, Schneiderat P, Ensini M, Garavaglia B, Gurwitz D, Johnson D, Muntoni F, Puymirat J, Reza M, Voit T, Baldo C, Bricarelli FD, Goldwurm S, Merla G, Pegoraro E, Renieri A, Zatloukal K, Filocamo M, Lochmüller H. Mora M, et al. Among authors: bricarelli fd. Eur J Hum Genet. 2015 Sep;23(9):1116-23. doi: 10.1038/ejhg.2014.272. Epub 2014 Dec 24. Eur J Hum Genet. 2015. PMID: 25537360 Free PMC article.
Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases.
Filocamo M, Baldo C, Goldwurm S, Renieri A, Angelini C, Moggio M, Mora M, Merla G, Politano L, Garavaglia B, Casareto L, Bricarelli FD; Telethon Network of Genetic Biobanks Staff. Filocamo M, et al. Among authors: bricarelli fd. Orphanet J Rare Dis. 2013 Aug 30;8:129. doi: 10.1186/1750-1172-8-129. Orphanet J Rare Dis. 2013. PMID: 24004821 Free PMC article.
49 results