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

Year Number of Results
1945 2
1946 1
1949 1
1952 1
1954 1
1956 2
1957 2
1958 1
1960 2
1963 1
1964 1
1965 1
1969 1
1970 1
1971 2
1972 2
1973 1
1974 2
1976 1
1977 7
1978 2
1979 3
1980 2
1981 2
1982 1
1983 3
1984 4
1985 7
1986 3
1987 5
1988 4
1989 7
1990 4
1991 3
1992 3
1993 7
1994 8
1995 4
1996 19
1997 11
1998 12
1999 19
2000 36
2001 24
2002 17
2003 15
2004 20
2005 35
2006 43
2007 36
2008 50
2009 59
2010 34
2011 41
2012 49
2013 60
2014 56
2015 58
2016 53
2017 59
2018 68
2019 70
2020 61
2021 46
2022 39
2023 41
2024 44

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1,202 results

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Page 1
TDP-43 forms amyloid filaments with a distinct fold in type A FTLD-TDP.
Arseni D, Chen R, Murzin AG, Peak-Chew SY, Garringer HJ, Newell KL, Kametani F, Robinson AC, Vidal R, Ghetti B, Hasegawa M, Ryskeldi-Falcon B. Arseni D, et al. Among authors: vidal r. Nature. 2023 Aug;620(7975):898-903. doi: 10.1038/s41586-023-06405-w. Epub 2023 Aug 2. Nature. 2023. PMID: 37532939 Free PMC article.
Hereditary ferritinopathy.
Vidal R, Delisle MB, Rascol O, Ghetti B. Vidal R, et al. J Neurol Sci. 2003 Mar 15;207(1-2):110-1. doi: 10.1016/s0022-510x(02)00435-5. J Neurol Sci. 2003. PMID: 12614943 Review. No abstract available.
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients.
Borràs N, Batlle J, Pérez-Rodríguez A, López-Fernández MF, Rodríguez-Trillo Á, Lourés E, Cid AR, Bonanad S, Cabrera N, Moret A, Parra R, Mingot-Castellano ME, Balda I, Altisent C, Pérez-Montes R, Fisac RM, Iruín G, Herrero S, Soto I, de Rueda B, Jiménez-Yuste V, Alonso N, Vilariño D, Arija O, Campos R, Paloma MJ, Bermejo N, Berrueco R, Mateo J, Arribalzaga K, Marco P, Palomo Á, Sarmiento L, Iñigo B, Nieto MDM, Vidal R, Martínez MP, Aguinaco R, César JM, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Cornudella R, Aguilar C, Vidal F, Corrales I. Borràs N, et al. Among authors: vidal r. Haematologica. 2017 Dec;102(12):2005-2014. doi: 10.3324/haematol.2017.168765. Epub 2017 Sep 29. Haematologica. 2017. PMID: 28971901 Free PMC article.
Mutation ∆K281 in MAPT causes Pick's disease.
Schweighauser M, Garringer HJ, Klingstedt T, Nilsson KPR, Masuda-Suzukake M, Murrell JR, Risacher SL, Vidal R, Scheres SHW, Goedert M, Ghetti B, Newell KL. Schweighauser M, et al. Among authors: vidal r. Acta Neuropathol. 2023 Aug;146(2):211-226. doi: 10.1007/s00401-023-02598-6. Epub 2023 Jun 23. Acta Neuropathol. 2023. PMID: 37351604 Free PMC article.
Norovirus vaccines under development.
Lucero Y, Vidal R, O'Ryan G M. Lucero Y, et al. Among authors: vidal r. Vaccine. 2018 Aug 28;36(36):5435-5441. doi: 10.1016/j.vaccine.2017.06.043. Epub 2017 Jun 28. Vaccine. 2018. PMID: 28668568
Modeling familial British and Danish dementia.
Garringer HJ, Murrell J, D'Adamio L, Ghetti B, Vidal R. Garringer HJ, et al. Among authors: vidal r. Brain Struct Funct. 2010 Mar;214(2-3):235-44. doi: 10.1007/s00429-009-0221-9. Epub 2009 Sep 25. Brain Struct Funct. 2010. PMID: 19779737 Free PMC article. Review.
Functional Annotation of All Salmonid Genomes (FAASG): an international initiative supporting future salmonid research, conservation and aquaculture.
Macqueen DJ, Primmer CR, Houston RD, Nowak BF, Bernatchez L, Bergseth S, Davidson WS, Gallardo-Escárate C, Goldammer T, Guiguen Y, Iturra P, Kijas JW, Koop BF, Lien S, Maass A, Martin SAM, McGinnity P, Montecino M, Naish KA, Nichols KM, Ólafsson K, Omholt SW, Palti Y, Plastow GS, Rexroad CE Rd, Rise ML, Ritchie RJ, Sandve SR, Schulte PM, Tello A, Vidal R, Vik JO, Wargelius A, Yáñez JM; FAASG Consortium. Macqueen DJ, et al. Among authors: vidal r. BMC Genomics. 2017 Jun 27;18(1):484. doi: 10.1186/s12864-017-3862-8. BMC Genomics. 2017. PMID: 28655320 Free PMC article.
1,202 results