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

Year Number of Results
1947 1
1948 1
1951 1
1952 2
1957 1
1958 1
1960 2
1961 3
1962 1
1967 1
1968 3
1969 5
1970 4
1971 2
1975 2
1976 1
1978 4
1979 9
1980 11
1981 2
1982 8
1983 6
1984 10
1985 6
1986 23
1987 10
1988 14
1989 19
1990 14
1991 15
1992 18
1993 15
1994 19
1995 13
1996 6
1997 14
1998 22
1999 16
2000 14
2001 17
2002 20
2003 12
2004 21
2005 15
2006 22
2007 26
2008 22
2009 26
2010 59
2011 51
2012 61
2013 68
2014 61
2015 55
2016 53
2017 50
2018 50
2019 41
2020 62
2021 45
2022 48
2023 42
2024 31

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1,149 results

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Page 1
Remnant cholesterol, vascular risk, and prevention of atherosclerosis.
Pintó X, Fanlo M, Esteve V, Millán J; Grupo de Trabajo Dislipemia Aterogénica, Sociedad Española de Arteriosclerosis (SEA). Pintó X, et al. Among authors: millan j. Clin Investig Arterioscler. 2023 Jul-Aug;35(4):206-217. doi: 10.1016/j.arteri.2023.02.001. Epub 2023 Mar 6. Clin Investig Arterioscler. 2023. PMID: 36889989 Review. English, Spanish.
Usher Syndrome: Genetics of a Human Ciliopathy.
Fuster-García C, García-Bohórquez B, Rodríguez-Muñoz A, Aller E, Jaijo T, Millán JM, García-García G. Fuster-García C, et al. Among authors: millan jm. Int J Mol Sci. 2021 Jun 23;22(13):6723. doi: 10.3390/ijms22136723. Int J Mol Sci. 2021. PMID: 34201633 Free PMC article. Review.
Preface.
Ramsey NF, Millán JDR. Ramsey NF, et al. Among authors: millan jdr. Handb Clin Neurol. 2020;168:ix-x. doi: 10.1016/B978-0-444-63934-9.09984-4. Handb Clin Neurol. 2020. PMID: 32164871 No abstract available.
Targeted next generation sequencing for molecular diagnosis of Usher syndrome.
Aparisi MJ, Aller E, Fuster-García C, García-García G, Rodrigo R, Vázquez-Manrique RP, Blanco-Kelly F, Ayuso C, Roux AF, Jaijo T, Millán JM. Aparisi MJ, et al. Among authors: millan jm. Orphanet J Rare Dis. 2014 Nov 18;9:168. doi: 10.1186/s13023-014-0168-7. Orphanet J Rare Dis. 2014. PMID: 25404053 Free PMC article.
Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases.
Calucho M, Bernal S, Alías L, March F, Venceslá A, Rodríguez-Álvarez FJ, Aller E, Fernández RM, Borrego S, Millán JM, Hernández-Chico C, Cuscó I, Fuentes-Prior P, Tizzano EF. Calucho M, et al. Among authors: millan jm. Neuromuscul Disord. 2018 Mar;28(3):208-215. doi: 10.1016/j.nmd.2018.01.003. Epub 2018 Jan 11. Neuromuscul Disord. 2018. PMID: 29433793
Redox Status in Retinitis Pigmentosa.
Olivares-González L, Velasco S, Campillo I, Millán JM, Rodrigo R. Olivares-González L, et al. Among authors: millan jm. Adv Exp Med Biol. 2023;1415:443-448. doi: 10.1007/978-3-031-27681-1_65. Adv Exp Med Biol. 2023. PMID: 37440070 Review.
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative.
Luque J, Mendes I, Gómez B, Morte B, López de Heredia M, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F; CIBERER Network; Lapunzina P. Luque J, et al. Among authors: millan jm. Clin Genet. 2022 May;101(5-6):481-493. doi: 10.1111/cge.14113. Epub 2022 Feb 4. Clin Genet. 2022. PMID: 35060122 Free PMC article. Review.
Molecular Insights of Cholestasis in MDR2 Knockout Murine Liver Organoids.
Blázquez-García I, Guerrero L, Cacho-Navas C, Djouder N, Millan J, Paradela A, Carmona-Rodríguez L, Corrales FJ. Blázquez-García I, et al. Among authors: millan j. J Proteome Res. 2024 Apr 5;23(4):1433-1442. doi: 10.1021/acs.jproteome.3c00900. Epub 2024 Mar 15. J Proteome Res. 2024. PMID: 38488493 Free PMC article.
1,149 results