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Page 1
Screening for SCA27B, CANVAS and other repeat expansion disorders in Greek patients with late-onset cerebellar ataxia suggests a need to update current diagnostic algorithms.
Koutsis G, Kartanou C, Kontogeorgiou Z, Koniari C, Mitrousias A, Pellerin D, Dicaire MJ, Iruzubieta P, Danzi MC, Athanassopoulos K, Ragazos N, Stamelou M, Rentzos M, Anagnostou E, Zuchner S, Brais B, Houlden H, Panas M, Stefanis L, Karadima G. Koutsis G, et al. Among authors: stamelou m. J Neurol Sci. 2024 Nov 15;467:123309. doi: 10.1016/j.jns.2024.123309. Online ahead of print. J Neurol Sci. 2024. PMID: 39571249
External Factors Modulating Pain and Pain-Related Functional Impairment in Cervical Dystonia.
Martino D, Achen BMC, Morgante F, Erro R, Fox SH, Edwards MJ, Schrag A, Stamelou M, Appel-Cresswell S, Defazio G, Ray-Chaudhuri K, Poplawska-Domaszewicz K, Richardson SP, Jinnah HA, Bruno VA. Martino D, et al. Among authors: stamelou m. Mov Disord Clin Pract. 2024 Oct 23. doi: 10.1002/mdc3.14235. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 39440662
Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.
Wang H, Chang TS, Dombroski BA, Cheng PL, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Rajput A, De Deyn PP, Le Bastard N, Gearing M, Kaat LD, Van Swieten JC, Dopper E, Ghetti BF, Newell KL, Troakes C, de Yébenes JG, Rábano-Gutierrez A, Meller T, Oertel WH, Respondek G, Stamelou M, Arzberger T, Roeber S, Müller U, Hopfner F, Pastor P, Brice A, Durr A, Le Ber I, Beach TG, Serrano GE, Hazrati LN, Litvan I, Rademakers R, Ross OA, Galasko D, Boxer AL, Miller BL, Seeley WW, Van Deerlin VM, Lee EB, White CL 3rd, Morris H, de Silva R, Crary JF, Goate AM, Friedman JS, Leung YY, Coppola G, Naj AC, Wang LS; P. S. P. genetics study group; Dalgard C, Dickson DW, Höglinger GU, Schellenberg GD, Geschwind DH, Lee WP. Wang H, et al. Among authors: stamelou m. Mol Neurodegener. 2024 Oct 14;19(1):73. doi: 10.1186/s13024-024-00763-3. Mol Neurodegener. 2024. PMID: 39402686 Free PMC article. No abstract available.
Precision Dopaminergic Treatment in a Cohort of Parkinson's Disease Patients Carrying Autosomal Recessive Gene Variants: Clinical Cohort Data and a Mini Review.
Koros C, Simitsi AM, Papagiannakis N, Bougea A, Antonelou R, Pachi I, Sfikas E, Stanitsa E, Angelopoulou E, Constantinides VC, Papageorgiou SG, Potagas C, Stamelou M, Stefanis L. Koros C, et al. Among authors: stamelou m. Neurol Int. 2024 Jul 30;16(4):833-844. doi: 10.3390/neurolint16040062. Neurol Int. 2024. PMID: 39195564 Free PMC article.
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.
Wang H, Chang TS, Dombroski BA, Cheng PL, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Rajput A, De Deyn PP, Le Bastard N, Gearing M, Kaat LD, Van Swieten JC, Dopper E, Ghetti BF, Newell KL, Troakes C, de Yébenes JG, Rábano-Gutierrez A, Meller T, Oertel WH, Respondek G, Stamelou M, Arzberger T, Roeber S, Müller U, Hopfner F, Pastor P, Brice A, Durr A, Le Ber I, Beach TG, Serrano GE, Hazrati LN, Litvan I, Rademakers R, Ross OA, Galasko D, Boxer AL, Miller BL, Seeley WW, Van Deerlin VM, Lee EB, White CL 3rd, Morris H, de Silva R, Crary JF, Goate AM, Friedman JS, Leung YY, Coppola G, Naj AC, Wang LS; P. S. P. genetics study group; Dalgard C, Dickson DW, Höglinger GU, Schellenberg GD, Geschwind DH, Lee WP. Wang H, et al. Among authors: stamelou m. Mol Neurodegener. 2024 Aug 16;19(1):61. doi: 10.1186/s13024-024-00747-3. Mol Neurodegener. 2024. PMID: 39152475 Free PMC article.
Functional neurological disorder in Europe: regional differences in education and health policy.
Serranová T, Di Vico I, Tinazzi M, Aybek S, Bilic E, Binzer S, Bøen E, Bruggeman A, Bratanov C, Cabreira VRA, Golder D, Dunalska A, Falup-Pecurariu C, Garcin B, Gelauff J, Laffan A, Podnar S, Pareés I, Plender T, Popkirov S, Romanenko V, Schwingenschuh P, Seliverstov Y, Sjöström C, Škorvánek M, Stamelou M, Zailskas D, Edwards MJ, Stone J. Serranová T, et al. Among authors: stamelou m. Eur J Neurol. 2024 Oct;31(10):e16350. doi: 10.1111/ene.16350. Epub 2024 Aug 15. Eur J Neurol. 2024. PMID: 39145716 Free PMC article.
Ethnic Differences in Atypical Parkinsonism-is South Asian PSP Different?
Balint B, Neo S, Magrinelli F, Mulroy E, Latorre A, Stamelou M, Morris HR, Batla A, Bhatia KP. Balint B, et al. Among authors: stamelou m. Mov Disord Clin Pract. 2024 Nov;11(11):1355-1364. doi: 10.1002/mdc3.14182. Epub 2024 Aug 7. Mov Disord Clin Pract. 2024. PMID: 39113437 Free PMC article.
Magnetic Resonance Imaging Measures to Track Atrophy Progression in Progressive Supranuclear Palsy in Clinical Trials.
Quattrone A, Franzmeier N, Huppertz HJ, Klietz M, Roemer SN, Boxer AL, Levin J, Höglinger GU; AL‐108‐231 Investigators, the Tauros MRI Investigators, the PASSPORT Study Group, the DESCRIBE‐PSP Group. Quattrone A, et al. Mov Disord. 2024 Aug;39(8):1329-1342. doi: 10.1002/mds.29866. Epub 2024 Jun 2. Mov Disord. 2024. PMID: 38825840
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes.
Wang H, Chang TS, Dombroski BA, Cheng PL, Si YQ, Tucci A, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Alex R, Paul De Deyn P, Le Bastard N, Gearing M, Donker Kaat L, Van Swieten JC, Dopper E, Ghetti BF, Newell KL, Troakes C, G de Yébenes J, Rábano-Gutierrez A, Meller T, Oertel WH, Respondek G, Stamelou M, Arzberger T, Roeber S, Müller U, Hopfner F, Pastor P, Brice A, Durr A, Ber IL, Beach TG, Serrano GE, Hazrati LN, Litvan I, Rademakers R, Ross OA, Galasko D, Boxer AL, Miller BL, Seeley WW, Van Deerlin VM, Lee EB, White CL 3rd, Morris HR, de Silva R, Crary JF, Goate AM, Friedman JS, Leung YY, Coppola G, Naj AC, Wang LS; PSP genetics study group; Dickson DW, Höglinger GU, Tzeng JY, Geschwind DH, Schellenberg GD, Lee WP. Wang H, et al. Among authors: stamelou m. medRxiv [Preprint]. 2024 Feb 28:2024.02.26.24303379. doi: 10.1101/2024.02.26.24303379. medRxiv. 2024. PMID: 38464214 Free PMC article. Preprint.
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians.
Ojo OO, Bandres-Ciga S, Makarious MB, Crea PW, Hernandez DG, Houlden H, Rizig M, Singleton AB, Noyce AJ, Nalls MA, Blauwendraat C, Okubadejo NU; Nigeria Parkinson's Disease Research Network and the Global Parkinson's Genetics Program (GP2). Ojo OO, et al. Mov Disord. 2024 Apr;39(4):728-733. doi: 10.1002/mds.29753. Epub 2024 Feb 23. Mov Disord. 2024. PMID: 38390630
208 results