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

Year Number of Results
1977 2
1978 1
1980 1
1981 3
1982 1
1985 1
1992 1
1999 1
2001 2
2002 1
2007 2
2009 2
2011 1
2012 1
2013 1
2014 2
2015 2
2024 0

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23 results

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Page 1
A novel mutation and novel features in Nijmegen breakage syndrome.
Maraschio P, Danesino C, Antoccia A, Ricordy R, Tanzarella C, Varon R, Reis A, Besana D, Guala A, Tiepolo L. Maraschio P, et al. Among authors: besana d. J Med Genet. 2001 Feb;38(2):113-7. doi: 10.1136/jmg.38.2.113. J Med Genet. 2001. PMID: 11288710 Free PMC article. No abstract available.
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.
Annesi F, Gambardella A, Michelucci R, Bianchi A, Marini C, Canevini MP, Capovilla G, Elia M, Buti D, Chifari R, Striano P, Rocca FE, Castellotti B, Cali F, Labate A, LePiane E, Besana D, Sofia V, Tabiadon G, Tortorella G, Vigliano P, Vignoli A, Beccaria F, Annesi G, Striano S, Aguglia U, Guerrini R, Quattrone A. Annesi F, et al. Among authors: besana d. Epilepsia. 2007 Sep;48(9):1686-1690. doi: 10.1111/j.1528-1167.2007.01173.x. Epub 2007 Jul 18. Epilepsia. 2007. PMID: 17634063 Free article.
[Prevention of neuromuscular diseases].
Lanzi G, Besana D. Lanzi G, et al. Among authors: besana d. Minerva Pediatr. 1981 Jul 15;33(13):621-6. Minerva Pediatr. 1981. PMID: 7022159 Review. Italian. No abstract available.
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy.
Striano P, Coppola A, Pezzella M, Ciampa C, Specchio N, Ragona F, Mancardi MM, Gennaro E, Beccaria F, Capovilla G, Rasmini P, Besana D, Coppola GG, Elia M, Granata T, Vecchi M, Vigevano F, Viri M, Gaggero R, Striano S, Zara F. Striano P, et al. Among authors: besana d. Neurology. 2007 Jul 17;69(3):250-4. doi: 10.1212/01.wnl.0000265222.24102.db. Neurology. 2007. PMID: 17636062 Clinical Trial.
23 results