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MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh.
De Benedittis S, Spadafora P, Gaspari M, Qualtieri G, Gallo O, Di Palma G, Cavalcanti F, Citrigno L, Qualtieri A. De Benedittis S, et al. Among authors: spadafora p. Clin Chem Lab Med. 2023 Jun 12;61(12):e251-e254. doi: 10.1515/cclm-2023-0442. Print 2023 Nov 27. Clin Chem Lab Med. 2023. PMID: 37307396 No abstract available.
Association of tau gene polymorphism with Parkinson's disease.
Zappia M, Annesi G, Nicoletti G, Serra P, Arabia G, Pugliese P, Messina D, Caracciolo M, Romeo N, Annesi F, Pasqua AA, Spadafora P, Civitelli D, Romeo N, Epifanio A, Morgante L, Quattrone A. Zappia M, et al. Among authors: spadafora p. Neurol Sci. 2003 Oct;24(3):223-4. doi: 10.1007/s10072-003-0141-z. Neurol Sci. 2003. PMID: 14600827
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit.
Annesi G, Sofia V, Gambardella A, Candiano IC, Spadafora P, Annesi F, Cutuli N, De Marco EV, Civitelli D, Carrideo S, Tarantino P, Barone R, Zappia M, Quattrone A. Annesi G, et al. Among authors: spadafora p. Epilepsia. 2004 Mar;45(3):294-5. doi: 10.1111/j.0013-9580.2004.33203.x. Epilepsia. 2004. PMID: 15009235 Free article. 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.
57 results