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

Year Number of Results
2002 1
2003 1
2004 3
2005 1
2006 1
2007 1
2008 1
2011 1
2012 1
2014 1
2015 1
2016 2
2018 1
2020 1
2021 1
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17 results
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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. 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.
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders.
La Cognata V, Morello G, Gentile G, Cavalcanti F, Cittadella R, Conforti FL, De Marco EV, Magariello A, Muglia M, Patitucci A, Spadafora P, D'Agata V, Ruggieri M, Cavallaro S. La Cognata V, et al. Among authors: spadafora p. Curr Genomics. 2018 Sep;19(6):431-443. doi: 10.2174/1389202919666180404105451. Curr Genomics. 2018. PMID: 30258275 Free PMC article.
Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
Valentino P, Annesi G, Cirò Candiano IC, Annesi F, Civitelli D, Tarantino P, Naso F, Spadafora P, Carrideo S, De Marco EV, Consoli D, Zappia M, Gambardella A, Quattrone A. Valentino P, et al. Among authors: spadafora p. Mov Disord. 2006 Feb;21(2):252-4. doi: 10.1002/mds.20681. Mov Disord. 2006. PMID: 16149094
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.
Annesi G, Gambardella A, Carrideo S, Incorpora G, Labate A, Pasqua AA, Civitelli D, Polizzi A, Annesi F, Spadafora P, Tarantino P, Cirò Candiano IC, Romeo N, De Marco EV, Ventura P, LePiane E, Zappia M, Aguglia U, Pavone L, Quattrone A. Annesi G, et al. Among authors: spadafora p. Epilepsia. 2003 Sep;44(9):1257-8. doi: 10.1046/j.1528-1157.2003.22503.x. Epilepsia. 2003. PMID: 12919402 Free article. No abstract available.
17 results