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Page 1
Protein Binding Partners of Dysregulated miRNAs in Parkinson's Disease Serum.
Ruf WP, Freischmidt A, Grozdanov V, Roth V, Brockmann SJ, Mollenhauer B, Martin D, Haslinger B, Fundel-Clemens K, Otto M, Arnim CV, Holzmann K, Ludolph AC, Weishaupt JH, Danzer KM. Ruf WP, et al. Among authors: roth v. Cells. 2021 Apr 2;10(4):791. doi: 10.3390/cells10040791. Cells. 2021. PMID: 33918274 Free PMC article.
Inflammatory dysregulation of blood monocytes in Parkinson's disease patients.
Grozdanov V, Bliederhaeuser C, Ruf WP, Roth V, Fundel-Clemens K, Zondler L, Brenner D, Martin-Villalba A, Hengerer B, Kassubek J, Ludolph AC, Weishaupt JH, Danzer KM. Grozdanov V, et al. Among authors: roth v. Acta Neuropathol. 2014 Nov;128(5):651-63. doi: 10.1007/s00401-014-1345-4. Epub 2014 Oct 5. Acta Neuropathol. 2014. PMID: 25284487 Free PMC article.
Oculomotor Findings in Spinocerebellar Ataxia 27B: A Case Series.
Clément G, Puisieux S, Ashton C, Pellerin D, Danzi MC, Bonnet C, Roth V, Wandzel M, Hocquel A, Pourié C, Dreumont N, Lambert L, Houlden H, Zuchner S, Brais B, Rejeb IB, Frismand S, Renaud M. Clément G, et al. Among authors: roth v. Can J Neurol Sci. 2024 Dec 9:1-3. doi: 10.1017/cjn.2024.355. Online ahead of print. Can J Neurol Sci. 2024. PMID: 39648743 No abstract available.
Detection of a Water-Soluble Hypericin Formulation in Glioblastoma Tissue with Fluorescence Lifetime and Intensity Using a Dual-Tap CMOS Camera System.
Mischkulnig M, Reichert D, Wightman L, Roth V, Hölz M, Körner LI, Kiesel B, Vejzovic D, Giardina GA, Erkkilae MT, Unterhuber A, Andreana M, Rinner B, Kubin A, Leitgeb R, Widhalm G. Mischkulnig M, et al. Among authors: roth v. Diagnostics (Basel). 2024 Oct 30;14(21):2423. doi: 10.3390/diagnostics14212423. Diagnostics (Basel). 2024. PMID: 39518390 Free PMC article.
A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus.
Pellerin D, Del Gobbo GF, Couse M, Dolzhenko E, Nageshwaran SK, Cheung WA, Xu IRL, Dicaire MJ, Spurdens G, Matos-Rodrigues G, Stevanovski I, Scriba CK, Rebelo A, Roth V, Wandzel M, Bonnet C, Ashton C, Agarwal A, Peter C, Hasson D, Tsankova NM, Dewar K, Lamont PJ, Laing NG, Renaud M, Houlden H, Synofzik M, Usdin K, Nussenzweig A, Napierala M, Chen Z, Jiang H, Deveson IW, Ravenscroft G, Akbarian S, Eberle MA, Boycott KM, Pastinen T; All of Us Research Program Long Read Working Group; Brais B, Zuchner S, Danzi MC. Pellerin D, et al. Among authors: roth v. Nat Genet. 2024 Jul;56(7):1366-1370. doi: 10.1038/s41588-024-01808-5. Epub 2024 Jun 27. Nat Genet. 2024. PMID: 38937606 Free PMC article.
Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients.
Thomas H, Alix T, Renard É, Renaud M, Wourms J, Zuily S, Leheup B, Geneviève D, Dreumont N, Schmitt E, Bronner M, Muller M, Divoux M, Wandzel M, Ravel JM, Dexheimer M, Becker A, Roth V, Willems M, Coubes C, Vieville G, Devillard F, Schaefer É, Baer S, Piton A, Gérard B, Vincent M, Nizon M, Cogné B, Ruaud L, Couque N, Putoux A, Edery P, Lesca G, Chatron N, Till M, Faivre L, Tran-Mau-Them F, Alessandri JL, Lebrun M, Quélin C, Odent S, Dubourg C, David V, Faoucher M, Mignot C, Keren B, Pisan É, Afenjar A, Julia S, Bieth É, Banneau G, Goldenberg A, Husson T, Campion D, Lecoquierre F, Nicolas G, Charbonnier C, De Saint Martin A, Naudion S, Degoutin M, Rondeau S, Michot C, Cormier-Daire V, Oussalah A, Pourié C, Lambert L, Bonnet C. Thomas H, et al. Among authors: roth v. J Med Genet. 2024 Aug 29;61(9):878-885. doi: 10.1136/jmg-2024-110031. J Med Genet. 2024. PMID: 38937076 Free article.
226 results