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

Year Number of Results
2002 1
2003 1
2005 1
2006 2
2008 4
2009 3
2010 3
2011 1
2012 3
2013 5
2014 5
2015 6
2016 3
2017 8
2018 7
2019 4
2020 8
2021 10
2022 1
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Search Results

68 results
Results by year
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Page 1
Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation.
Frasquet M, Rojas-García R, Argente-Escrig H, Vázquez-Costa JF, Muelas N, Vílchez JJ, Sivera R, Millet E, Barreiro M, Díaz-Manera J, Turon-Sans J, Cortés-Vicente E, Querol L, Ramírez-Jiménez L, Martínez-Rubio D, Sánchez-Monteagudo A, Espinós C, Sevilla T, Lupo V. Frasquet M, et al. Among authors: espinos c. Eur J Neurol. 2021 Apr;28(4):1334-1343. doi: 10.1111/ene.14700. Epub 2021 Jan 10. Eur J Neurol. 2021. PMID: 33369814
Autosomal recessive Charcot-Marie-Tooth neuropathy.
Espinós C, Calpena E, Martínez-Rubio D, Lupo V. Espinós C, et al. Adv Exp Med Biol. 2012;724:61-75. doi: 10.1007/978-1-4614-0653-2_5. Adv Exp Med Biol. 2012. PMID: 22411234 Review.
Molecular diagnosis of coenzyme Q10 deficiency.
Yubero D, Montero R, Armstrong J, Espinós C, Palau F, Santos-Ocaña C, Salviati L, Navas P, Artuch R. Yubero D, et al. Among authors: espinos c. Expert Rev Mol Diagn. 2015;15(8):1049-59. doi: 10.1586/14737159.2015.1062727. Epub 2015 Jul 4. Expert Rev Mol Diagn. 2015. PMID: 26144946 Review.
Wilson's Disease: Facing the Challenge of Diagnosing a Rare Disease.
Sánchez-Monteagudo A, Ripollés E, Berenguer M, Espinós C. Sánchez-Monteagudo A, et al. Among authors: espinos c. Biomedicines. 2021 Aug 28;9(9):1100. doi: 10.3390/biomedicines9091100. Biomedicines. 2021. PMID: 34572285 Free PMC article. Review.
Charcot-Marie-Tooth disease due to MORC2 mutations in Spain.
Sivera R, Lupo V, Frasquet M, Argente-Escrig H, Alonso-Pérez J, Díaz-Manera J, Querol L, Del Mar García-Romero M, Ignacio Pascual S, García-Sobrino T, Paradas C, Francisco Vázquez-Costa J, Muelas N, Millet E, Jesús Vílchez J, Espinós C, Sevilla T. Sivera R, et al. Among authors: espinos c. Eur J Neurol. 2021 Sep;28(9):3001-3011. doi: 10.1111/ene.15001. Epub 2021 Jul 18. Eur J Neurol. 2021. PMID: 34189813
Chaperonopathies: Spotlight on Hereditary Motor Neuropathies.
Lupo V, Aguado C, Knecht E, Espinós C. Lupo V, et al. Among authors: espinos c. Front Mol Biosci. 2016 Dec 14;3:81. doi: 10.3389/fmolb.2016.00081. eCollection 2016. Front Mol Biosci. 2016. PMID: 28018906 Free PMC article. Review.
Autosomal recessive cerebellar ataxias.
Palau F, Espinós C. Palau F, et al. Among authors: espinos c. Orphanet J Rare Dis. 2006 Nov 17;1:47. doi: 10.1186/1750-1172-1-47. Orphanet J Rare Dis. 2006. PMID: 17112370 Free PMC article. Review.
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. Antioxidants (Basel). 2020 Apr 15;9(4):313. doi: 10.3390/antiox9040313. Antioxidants (Basel). 2020. PMID: 32326494 Free PMC article. Review.
68 results