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The LINCE Project: A Pathway for Diagnosing NCL2 Disease.
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.
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Etiology of avascular necrosis of the hip and shoulder. Screening for Gaucher disease.
Cuenca-Gómez JÁ, Ocaña-Losada C, Crujeiras P, Rodrigues D, Martínez-Espinosa M.
Cuenca-Gómez JÁ, et al. Among authors: crujeiras p.
Rev Clin Esp (Barc). 2023 Jan;223(1):17-24. doi: 10.1016/j.rceng.2022.10.003. Epub 2022 Nov 26.
Rev Clin Esp (Barc). 2023.
PMID: 36457211
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Deactivation of the coordinating ability of the iminophosphorane group by the effect of ortho-carborane.
Crujeiras P, Rodríguez-Rey JL, Sousa-Pedrares A.
Crujeiras P, et al.
Dalton Trans. 2017 Feb 21;46(8):2572-2593. doi: 10.1039/c6dt04592h.
Dalton Trans. 2017.
PMID: 28154845
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