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

Year Number of Results
2002 1
2003 3
2004 3
2007 1
2008 2
2010 2
2011 3
2012 1
2013 1
2014 1
2017 1
2021 1
2022 0
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19 results
Results by year
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Page 1
CAV3 T78M mutation as polymorphic variant in South Italy.
Spadafora P, Liguori M, Andreoli V, Quattrone A, Gambardella A. Spadafora P, et al. Among authors: andreoli v. Neuromuscul Disord. 2012 Jul;22(7):669-70; author reply 670-1. doi: 10.1016/j.nmd.2012.03.007. Epub 2012 May 16. Neuromuscul Disord. 2012. PMID: 22595201 No abstract available.
Presenilin-2 gene mutation presenting as Lewy body dementia?
Raciti L, Nicoletti A, Le Pira F, Andreoli V, Contrafatto D, Lanzafame S, Maci T, Gambardella A, Quattrone A, Zappia M. Raciti L, et al. Among authors: andreoli v. Neurol Sci. 2011 Jun;32(3):533-4. doi: 10.1007/s10072-011-0497-4. Epub 2011 Mar 16. Neurol Sci. 2011. PMID: 21409510 No abstract available.
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy.
Gambardella A, Manna I, Labate A, Chifari R, Serra P, La Russa A, LePiane E, Cittadella R, Andreoli V, Sasanelli F, Zappia M, Aguglia U, Quattrone A. Gambardella A, et al. Among authors: andreoli v. Epilepsia. 2003 Sep;44(9):1255-6. doi: 10.1046/j.1528-1157.2003.18003.x. Epilepsia. 2003. PMID: 12919401 Free article. No abstract available.
19 results