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Silent celiac disease in patients with childhood localization-related epilepsies.
Labate A, Gambardella A, Messina D, Tammaro S, Le Piane E, Pirritano D, Cosco C, Doldo P, Mazzei R, Oliveri RL, Bosco D, Zappia M, Valentino P, Aguglia U, Quattrone A. Labate A, et al. Among authors: oliveri rl. Epilepsia. 2001 Sep;42(9):1153-5. doi: 10.1046/j.1528-1157.2001.45700.x. Epilepsia. 2001. PMID: 11580763 Free article.
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings.
Oliveri RL, Muglia M, De Stefano N, Mazzei R, Labate A, Conforti FL, Patitucci A, Gabriele AL, Tagarelli G, Magariello A, Zappia M, Gambardella A, Federico A, Quattrone A. Oliveri RL, et al. Arch Neurol. 2001 Sep;58(9):1418-22. doi: 10.1001/archneur.58.9.1418. Arch Neurol. 2001. PMID: 11559313
The parkin gene is not involved in late-onset Parkinson's disease.
Oliveri RL, Zappia M, Annesi G, Bosco D, Annesi F, Spadafora P, Pasqua AA, Tomaino C, Nicoletti G, Pirritano D, Labate A, Gambardella A, Logroscino G, Manobianca G, Epifanio A, Morgante L, Savettieri G, Quattrone A. Oliveri RL, et al. Neurology. 2001 Jul 24;57(2):359-62. doi: 10.1212/wnl.57.2.359. Neurology. 2001. PMID: 11468333
53 results