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Proteomics in Inherited Metabolic Disorders.
Chantada-Vázquez MDP, Bravo SB, Barbosa-Gouveia S, Alvarez JV, Couce ML. Chantada-Vázquez MDP, et al. Among authors: couce ml. Int J Mol Sci. 2022 Nov 25;23(23):14744. doi: 10.3390/ijms232314744. Int J Mol Sci. 2022. PMID: 36499071 Free PMC article. Review.
Identification of Clinical Variants beyond the Exome in Inborn Errors of Metabolism.
Soriano-Sexto A, Gallego D, Leal F, Castejón-Fernández N, Navarrete R, Alcaide P, Couce ML, Martín-Hernández E, Quijada-Fraile P, Peña-Quintana L, Yahyaoui R, Correcher P, Ugarte M, Rodríguez-Pombo P, Pérez B. Soriano-Sexto A, et al. Among authors: couce ml. Int J Mol Sci. 2022 Oct 25;23(21):12850. doi: 10.3390/ijms232112850. Int J Mol Sci. 2022. PMID: 36361642 Free PMC article.
Paediatric clinical study of 3D printed personalised medicines for rare metabolic disorders.
Rodríguez-Pombo L, de Castro-López MJ, Sánchez-Pintos P, Giraldez-Montero JM, Januskaite P, Duran-Piñeiro G, Dolores Bóveda M, Alvarez-Lorenzo C, Basit AW, Goyanes A, Couce ML. Rodríguez-Pombo L, et al. Among authors: couce ml. Int J Pharm. 2024 Apr 19;657:124140. doi: 10.1016/j.ijpharm.2024.124140. Online ahead of print. Int J Pharm. 2024. PMID: 38643809 Free article.
Editorial: NGS technologies of rare diseases diagnosis.
Couce ML, González-Vioque E. Couce ML, et al. Front Pediatr. 2022 Nov 12;10:1032359. doi: 10.3389/fped.2022.1032359. eCollection 2022. Front Pediatr. 2022. PMID: 36444169 Free PMC article. No abstract available.
246 results