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517 results

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Page 1
Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease.
Quattrone A, Bagnato A, Annesi G, Novellino F, Morgante L, Savettieri G, Zappia M, Tarantino P, Candiano IC, Annesi F, Civitelli D, Rocca FE, D'Amelio M, Nicoletti G, Morelli M, Petrone A, Loizzo P, Condino F. Quattrone A, et al. Among authors: zappia m. Mov Disord. 2008 Jan;23(1):21-7. doi: 10.1002/mds.21701. Mov Disord. 2008. PMID: 17975812
Body weight influences pharmacokinetics of levodopa in Parkinson's disease.
Zappia M, Crescibene L, Arabia G, Nicoletti G, Bagalà A, Bastone L, Caracciolo M, Bonavita S, Di Costanzo A, Scornaienchi M, Gambardella A, Quattrone A. Zappia M, et al. Clin Neuropharmacol. 2002 Mar-Apr;25(2):79-82. doi: 10.1097/00002826-200203000-00004. Clin Neuropharmacol. 2002. PMID: 11981233
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: zappia m. 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.
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: zappia m. 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.
Temporal lobe epilepsy as a unique manifestation of multiple sclerosis.
Gambardella A, Valentino P, Labate A, Sibilia G, Ruscica F, Colosimo E, Nisticò R, Messina D, Zappia M, Quattrone A. Gambardella A, et al. Among authors: zappia m. Can J Neurol Sci. 2003 Aug;30(3):228-32. doi: 10.1017/s031716710000264x. Can J Neurol Sci. 2003. PMID: 12945947
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: zappia m. 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.
517 results