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2020 | 3 |
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Page 1
Molecular characterization of Spanish patients with MECP2 duplication syndrome.
Clin Genet. 2020 Apr;97(4):610-620. doi: 10.1111/cge.13718. Epub 2020 Feb 23.
Clin Genet. 2020.
PMID: 32043567
Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism.
Castells AA, Gueraldi D, Balada R, Tristán-Noguero A, Cortès-Saladelafont E, Ramos F, Meavilla S, De Los Santos M, Garcia-Volpe C, Colomé R, Couce ML, Sierra C, Ormazábal A, Batllori M, Artuch R, Armstrong J, Alcántara S, Garcia-Cazorla À.
Castells AA, et al.
Sci Rep. 2019 Jun 24;9(1):9128. doi: 10.1038/s41598-019-45674-2.
Sci Rep. 2019.
PMID: 31235756
Free PMC article.
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Unraveling Molecular Pathways Altered in MeCP2-Related Syndromes, in the Search for New Potential Avenues for Therapy.
Castells AA, Balada R, Tristán-Noguero A, O'Callaghan M, Cortès-Saladelafont E, Pascual-Alonso A, Garcia-Cazorla À, Armstrong J, Alcántara S.
Castells AA, et al.
Biomedicines. 2021 Feb 3;9(2):148. doi: 10.3390/biomedicines9020148.
Biomedicines. 2021.
PMID: 33546327
Free PMC article.
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Enquiring beneath the surface: can a gene expression assay shed light into the heterogeneity among newborns with neonatal encephalopathy?
Balada R, Tebé C, León M, Arca G, Alsina M, Castells AA, Alcántara S, Garcia-Alix A.
Balada R, et al. Among authors: castells aa.
Pediatr Res. 2020 Sep;88(3):451-458. doi: 10.1038/s41390-020-0764-2. Epub 2020 Jan 17.
Pediatr Res. 2020.
PMID: 31952072
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Comprehensive Analysis of GABAA-A1R Developmental Alterations in Rett Syndrome: Setting the Focus for Therapeutic Targets in the Time Frame of the Disease.
Oyarzabal A, Xiol C, Castells AA, Grau C, O'Callaghan M, Fernández G, Alcántara S, Pineda M, Armstrong J, Altafaj X, García-Cazorla A.
Oyarzabal A, et al. Among authors: castells aa.
Int J Mol Sci. 2020 Jan 14;21(2):518. doi: 10.3390/ijms21020518.
Int J Mol Sci. 2020.
PMID: 31947619
Free PMC article.
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