Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
2001 1
2002 1
2003 2
2004 2
2005 5
2006 5
2007 4
2008 5
2009 6
2010 6
2011 6
2012 6
2013 6
2014 5
2015 6
2016 4
2017 5
2018 9
2019 8
2020 9
2021 14
Text availability
Article attribute
Article type
Publication date

Search Results

98 results
Results by year
Filters applied: . Clear all
Page 1
Ethical questions concerning newborn genetic screening.
Esquerda M, Palau F, Lorenzo D, Cambra FJ, Bofarull M, Cusi V, Interdisciplinar En Bioetica G. Esquerda M, et al. Among authors: palau f. Clin Genet. 2021 Jan;99(1):93-98. doi: 10.1111/cge.13828. Epub 2020 Sep 2. Clin Genet. 2021. PMID: 32779199 Review.
[Participant-funded clinical trials on rare diseases].
Dal-Ré R, Palau F, Guillén-Navarro E, Ayuso C. Dal-Ré R, et al. Among authors: palau f. An Pediatr (Engl Ed). 2020 Oct;93(4):267.e1-267.e9. doi: 10.1016/j.anpedi.2020.03.019. Epub 2020 Jun 1. An Pediatr (Engl Ed). 2020. PMID: 32499195 Free article. Spanish.
[The human genome and medicine].
Palau F, García-Alix A. Palau F, et al. An Pediatr (Engl Ed). 2018 Jul;89(1):1-2. doi: 10.1016/j.anpedi.2018.04.009. Epub 2018 May 10. An Pediatr (Engl Ed). 2018. PMID: 29753559 Free article. Spanish. No abstract available.
Cofilin dysregulation alters actin turnover in frataxin-deficient neurons.
Muñoz-Lasso DC, Mollá B, Calap-Quintana P, García-Giménez JL, Pallardo FV, Palau F, Gonzalez-Cabo P. Muñoz-Lasso DC, et al. Among authors: palau f. Sci Rep. 2020 Mar 23;10(1):5207. doi: 10.1038/s41598-020-62050-7. Sci Rep. 2020. PMID: 32251310 Free PMC article.
Epilepsy in LAMA2-related muscular dystrophy: An electro-clinico-radiological characterization.
Natera-de Benito D, Muchart J, Itzep D, Ortez C, González-Quereda L, Gallano P, Ramirez A, Aparicio J, Domínguez-Carral J, Carrera-García L, Expósito-Escudero J, Pardo Cardozo N, Cuadras D, Codina A, Jou C, Jimenez-Mallebrera C, Palau F, Colomer J, Arzimanoglou A, Nascimento A, San Antonio-Arce V. Natera-de Benito D, et al. Among authors: palau f. Epilepsia. 2020 May;61(5):971-983. doi: 10.1111/epi.16493. Epub 2020 Apr 8. Epilepsia. 2020. PMID: 32266982
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: palau f. 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.
Autosomal recessive cerebellar ataxias.
Palau F, Espinós C. Palau F, et al. 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.
Mitochondrial pathophysiology in Friedreich's ataxia.
González-Cabo P, Palau F. González-Cabo P, et al. Among authors: palau f. J Neurochem. 2013 Aug;126 Suppl 1:53-64. doi: 10.1111/jnc.12303. J Neurochem. 2013. PMID: 23859341 Free article. Review.
Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations.
Casas-Alba D, Martínez-Monseny A, Pino-Ramírez RM, Alsina L, Castejón E, Navarro-Vilarrubí S, Pérez-Dueñas B, Serrano M, Palau F, García-Alix A. Casas-Alba D, et al. Among authors: palau f. Hum Mutat. 2018 Dec;39(12):1752-1763. doi: 10.1002/humu.23638. Epub 2018 Sep 17. Hum Mutat. 2018. PMID: 30176098 Review.
98 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page