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The LINCE Project: A Pathway for Diagnosing NCL2 Disease.
Rodrigues D, de Castro MJ, Crujeiras P, Duat-Rodriguez A, Marco AV, Del Toro M, Couce ML, Colón C. Rodrigues D, et al. Among authors: crujeiras p. Front Pediatr. 2022 Mar 29;10:876688. doi: 10.3389/fped.2022.876688. eCollection 2022. Front Pediatr. 2022. PMID: 35425725 Free PMC article.
Family study of a novel mutation of mucopolysaccharidosis type VI with a severe phenotype and good response to enzymatic replacement therapy: Case report.
Ley-Martos M, Guerrero JM, Lucas-Javato M, Remón-García C, García-Lozano JR, Colón C, Crujeiras P, Rodrigues D, Paúl-Sánchez P, Macher HC. Ley-Martos M, et al. Among authors: crujeiras p. Medicine (Baltimore). 2018 Oct;97(42):e12872. doi: 10.1097/MD.0000000000012872. Medicine (Baltimore). 2018. PMID: 30335002 Free PMC article.