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Page 1
Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.
Marongiu R, Ghezzi D, Ialongo T, Soleti F, Elia A, Cavone S, Albanese A, Altavista MC, Barone P, Brusa L, Cortelli P, Petrozzi L, Scaglione C, Stanzione P, Tinazzi M, Zeviani M, Dallapiccola B, Bentivoglio AR, Valente EM, Garavaglia B; Italian PD Study Group. Marongiu R, et al. Mov Disord. 2006 Aug;21(8):1232-5. doi: 10.1002/mds.20890. Mov Disord. 2006. PMID: 16622859
Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.
Rossi G, Bastone A, Piccoli E, Morbin M, Mazzoleni G, Fugnanesi V, Beeg M, Del Favero E, Cantù L, Motta S, Salsano E, Pareyson D, Erbetta A, Elia AE, Del Sorbo F, Silani V, Morelli C, Salmona M, Tagliavini F. Rossi G, et al. Among authors: elia ae. Neurobiol Aging. 2014 Feb;35(2):408-17. doi: 10.1016/j.neurobiolaging.2013.08.004. Epub 2013 Sep 7. Neurobiol Aging. 2014. PMID: 24018212
Isolated limb dystonia as presenting feature of Parkin disease.
Elia AE, Del Sorbo F, Romito LM, Barzaghi C, Garavaglia B, Albanese A. Elia AE, et al. J Neurol Neurosurg Psychiatry. 2014 Jul;85(7):827-8. doi: 10.1136/jnnp-2013-307294. Epub 2014 Mar 21. J Neurol Neurosurg Psychiatry. 2014. PMID: 24659796 No abstract available.
Levodopa-carbidopa intrajejunal infusion in Parkinson's disease: untangling the role of age.
Morgante F, Oppo V, Fabbri M, Olivola E, Sorbera C, De Micco R, Ielo GC, Colucci F, Bonvegna S, Novelli A, Modugno N, Sensi M, Zibetti M, Lopiano L, Tessitore A, Pilleri M, Cilia R, Elia AE, Eleopra R, Ricciardi L, Cossu G. Morgante F, et al. Among authors: elia ae. J Neurol. 2021 May;268(5):1728-1737. doi: 10.1007/s00415-020-10356-x. Epub 2020 Dec 22. J Neurol. 2021. PMID: 33354739 Free PMC article.
106 results