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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
1952 1
1982 1
1983 1
1984 3
1985 1
1986 2
1989 3
1990 1
1992 1
1993 2
1994 2
1995 3
1996 1
1997 6
1998 10
1999 6
2000 2
2001 7
2002 5
2003 1
2004 5
2005 7
2006 7
2007 8
2008 4
2009 4
2010 21
2011 10
2012 12
2013 16
2014 11
2015 6
2016 11
2017 5
2018 8
2019 3
2020 10
2021 7
2022 11
2023 6
2024 3

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213 results

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Page 1
Brainstem stroke: anatomy, clinical and radiological findings.
Ortiz de Mendivil A, Alcalá-Galiano A, Ochoa M, Salvador E, Millán JM. Ortiz de Mendivil A, et al. Among authors: millan jm. Semin Ultrasound CT MR. 2013 Apr;34(2):131-41. doi: 10.1053/j.sult.2013.01.004. Semin Ultrasound CT MR. 2013. PMID: 23522778 Review.
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.
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.
Genetic Testing for Rare Diseases.
Millán JM, García-García G. Millán JM, et al. Diagnostics (Basel). 2022 Mar 25;12(4):809. doi: 10.3390/diagnostics12040809. Diagnostics (Basel). 2022. PMID: 35453856 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
TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa.
Bocquet B, Borday C, Erkilic N, Mamaeva D, Donval A, Masson C, Parain K, Kaminska K, Quinodoz M, Perea-Romero I, Garcia-Garcia G, Jimenez-Medina C, Boukhaddaoui H, Coget A, Leboucq N, Calzetti G, Gandolfi S, Percesepe A, Barili V, Uliana V, Delsante M, Bozzetti F, Scholl HP, Corton M, Ayuso C, Millan JM, Rivolta C, Meunier I, Perron M, Kalatzis V. Bocquet B, et al. Among authors: millan jm. JCI Insight. 2023 Nov 8;8(21):e169426. doi: 10.1172/jci.insight.169426. JCI Insight. 2023. PMID: 37768732 Free PMC article.
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.
Editorial: Inherited retinal dystrophies: a light at the end of the tunnel?
Perkins BD, Lobo GP, Kondkar AA, Millan JM. Perkins BD, et al. Among authors: millan jm. Front Cell Dev Biol. 2023 Oct 4;11:1301279. doi: 10.3389/fcell.2023.1301279. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37860821 Free PMC article. No abstract available.
213 results