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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1950 1
1952 1
1953 1
1955 1
1957 1
1959 1
1962 1
1971 1
1972 1
1976 1
1977 2
1979 1
1980 1
1981 2
1985 1
1991 1
1992 2
1995 1
1996 2
1997 2
1998 4
1999 2
2000 3
2001 6
2002 1
2003 3
2004 4
2005 6
2006 3
2007 11
2008 6
2009 10
2010 14
2011 7
2012 19
2013 13
2014 15
2015 9
2016 16
2017 10
2018 8
2019 8
2020 14
2021 10
2022 5
2023 12
2024 14
2025 6

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232 results

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Page 1
Concomitant Tricuspid Repair in Patients with Degenerative Mitral Regurgitation.
Gammie JS, Chu MWA, Falk V, Overbey JR, Moskowitz AJ, Gillinov M, Mack MJ, Voisine P, Krane M, Yerokun B, Bowdish ME, Conradi L, Bolling SF, Miller MA, Taddei-Peters WC, Jeffries NO, Parides MK, Weisel R, Jessup M, Rose EA, Mullen JC, Raymond S, Moquete EG, O'Sullivan K, Marks ME, Iribarne A, Beyersdorf F, Borger MA, Geirsson A, Bagiella E, Hung J, Gelijns AC, O'Gara PT, Ailawadi G; CTSN Investigators. Gammie JS, et al. N Engl J Med. 2022 Jan 27;386(4):327-339. doi: 10.1056/NEJMoa2115961. Epub 2021 Nov 13. N Engl J Med. 2022. PMID: 34767705 Free PMC article. Clinical Trial.
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.
Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophy.
Chelban V, Pellerin D, Vijiaratnam N, Lee H, Goh YY, Brown L, Sambin S, Seilhean D, Lehericy S, Iruzubieta P, Mohammad R, Self E, Scardamaglia A, Lee C, Ostrozovicova M, Dicaire MJ, Girges C, Gustavsson EK, Murphy D, Curless T, Laß J, Trinh J, Rittman T, Rowe JB, Hadjivassiliou M, Archibald N, Danzi MC, Ashton C, Roth V, Wandzel M, Cheung WA, Gveric DO, De Vil B, Follett J, Leigh PN, Beichert L, Pastinen T, Bonnet C, Renaud M, Meissner WG, Sieben A, Crosiers D, Cras P, Zuchner S, Corvol JC, Farrer MJ, Synofzik M, Brais B, Warner T, Morris HR, Jaunmuktane Z, Foltynie T, Houlden H. Chelban V, et al. Among authors: roth v. Brain. 2025 Sep 3;148(9):3252-3265. doi: 10.1093/brain/awaf134. Brain. 2025. PMID: 40239008 Free PMC article.
The generalized LASSO.
Roth V. Roth V. IEEE Trans Neural Netw. 2004 Jan;15(1):16-28. doi: 10.1109/TNN.2003.809398. IEEE Trans Neural Netw. 2004. PMID: 15387244
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.
Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions.
Méreaux JL, Davoine CS, Pellerin D, Coarelli G, Coutelier M, Ewenczyk C, Monin ML, Anheim M, Le Ber I, Thobois S, Gobert F, Guillot-Noël L, Forlani S, Jornea L, Heinzmann A, Sangare A, Gaymard B, Guyant-Maréchal L, Charles P, Marelli C, Honnorat J, Degos B, Tison F, Sangla S, Simonetta-Moreau M, Salachas F, Tchikviladzé M, Castelnovo G, Mochel F, Klebe S, Castrioto A, Fenu S, Méneret A, Bourdain F, Wandzel M, Roth V, Bonnet C, Riant F, Stevanin G, Noël S, Fauret-Amsellem AL, Bahlo M, Lockhart PJ, Brais B, Renaud M, Brice A, Durr A. Méreaux JL, et al. Among authors: roth v. EBioMedicine. 2024 Jan;99:104931. doi: 10.1016/j.ebiom.2023.104931. Epub 2023 Dec 27. EBioMedicine. 2024. PMID: 38150853 Free PMC article.
Occupational lead poisoning.
Staudinger KC, Roth VS. Staudinger KC, et al. Among authors: roth vs. Am Fam Physician. 1998 Feb 15;57(4):719-26, 731-2. Am Fam Physician. 1998. PMID: 9490995 Free article. Review.
[New approaches in speech therapy].
Pulvermüller F, Roth VM, Schönle PW. Pulvermüller F, et al. Among authors: roth vm. Nervenarzt. 1992 Mar;63(3):137-42. Nervenarzt. 1992. PMID: 1374536 Review. German.
Ocular tuberculosis: diagnostic and treatment challenges.
Alvarez GG, Roth VR, Hodge W. Alvarez GG, et al. Among authors: roth vr. Int J Infect Dis. 2009 Jul;13(4):432-5. doi: 10.1016/j.ijid.2008.09.018. Epub 2009 Apr 22. Int J Infect Dis. 2009. PMID: 19386531 Free article. Review. No abstract available.
232 results