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Page 1
Plasma Glutathione and Prodromal Parkinson's Disease Probability.
Charisis S, Ntanasi E, Stamelou M, Xiromerisiou G, Maraki M, Veskoukis AS, Yannakoulia M, Kosmidis MH, Anastasiou CA, Giagkou N, Dardiotis E, Hadjigeorgiou G, Sakka P, Kouretas D, Stefanis L, Scarmeas N. Charisis S, et al. Among authors: stamelou m. Mov Disord. 2022 Jan;37(1):200-205. doi: 10.1002/mds.28826. Epub 2021 Oct 25. Mov Disord. 2022. PMID: 34695238
THAP1 mutations and dystonia phenotypes: genotype phenotype correlations.
Xiromerisiou G, Houlden H, Scarmeas N, Stamelou M, Kara E, Hardy J, Lees AJ, Korlipara P, Limousin P, Paudel R, Hadjigeorgiou GM, Bhatia KP. Xiromerisiou G, et al. Among authors: stamelou m. Mov Disord. 2012 Sep 1;27(10):1290-4. doi: 10.1002/mds.25146. Epub 2012 Aug 17. Mov Disord. 2012. PMID: 22903657 Free PMC article. Review.
Functional movement disorders are not uncommon in the elderly.
Batla A, Stamelou M, Edwards MJ, Pareés I, Saifee TA, Fox Z, Bhatia KP. Batla A, et al. Among authors: stamelou m. Mov Disord. 2013 Apr;28(4):540-3. doi: 10.1002/mds.25350. Epub 2013 Feb 15. Mov Disord. 2013. PMID: 23418043
Familial psychogenic movement disorders.
Stamelou M, Cossu G, Edwards MJ, Murgia D, Pareés I, Melis M, Bhatia KP. Stamelou M, et al. Mov Disord. 2013 Aug;28(9):1295-8. doi: 10.1002/mds.25463. Epub 2013 Apr 8. Mov Disord. 2013. PMID: 23568243
The phenotypic spectrum of DYT24 due to ANO3 mutations.
Stamelou M, Charlesworth G, Cordivari C, Schneider SA, Kägi G, Sheerin UM, Rubio-Agusti I, Batla A, Houlden H, Wood NW, Bhatia KP. Stamelou M, et al. Mov Disord. 2014 Jun;29(7):928-34. doi: 10.1002/mds.25802. Epub 2014 Jan 17. Mov Disord. 2014. PMID: 24442708 Free PMC article.
Commentary.
Stamelou M. Stamelou M. Mov Disord. 2014 Mar;29(3):310. doi: 10.1002/mds.25848. Mov Disord. 2014. PMID: 24638846 No abstract available.
200 results