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Results by year

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 0
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Article attribute
Article type
Publication date

Search Results

204 results
Results by year
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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.
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.
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
Oxidative Stress, a Crossroad Between Rare Diseases and Neurodegeneration.
Espinós C, Galindo MI, García-Gimeno MA, Ibáñez-Cabellos JS, Martínez-Rubio D, Millán JM, Rodrigo R, Sanz P, Seco-Cervera M, Sevilla T, Tapia A, Pallardó FV. Espinós C, et al. Among authors: millan jm. Antioxidants (Basel). 2020 Apr 15;9(4):313. doi: 10.3390/antiox9040313. Antioxidants (Basel). 2020. PMID: 32326494 Free PMC article. Review.
Guidelines for genetic study of aniridia.
Blanco-Kelly F, Villaverde-Montero C, Lorda-Sánchez I, Millán JM, Trujillo-Tiebas MJ, Ayuso C. Blanco-Kelly F, et al. Among authors: millan jm. Arch Soc Esp Oftalmol. 2013 Apr;88(4):145-52. doi: 10.1016/j.oftal.2012.07.006. Epub 2012 Sep 25. Arch Soc Esp Oftalmol. 2013. PMID: 23597644 Review. English, Spanish.
[Molecular genetics of pigmentary retinopathy].
Millán JM, Nájera C, Beneyto M. Millán JM, et al. Med Clin (Barc). 1994 Jan 15;102(1):30-2. Med Clin (Barc). 1994. PMID: 8133683 Review. Spanish. No abstract available.
204 results