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Page 1
Secondary disorders of glycosylation in inborn errors of fructose metabolism.
Quintana E, Sturiale L, Montero R, Andrade F, Fernandez C, Couce ML, Barone R, Aldamiz-Echevarria L, Ribes A, Artuch R, Briones P. Quintana E, et al. Among authors: andrade f. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S273-8. doi: 10.1007/s10545-009-1219-4. Epub 2009 Sep 20. J Inherit Metab Dis. 2009. PMID: 19768653
Non-alcoholic fatty liver in hereditary fructose intolerance.
Aldámiz-Echevarría L, de Las Heras J, Couce ML, Alcalde C, Vitoria I, Bueno M, Blasco-Alonso J, Concepción García M, Ruiz M, Suárez R, Andrade F, Villate O. Aldámiz-Echevarría L, et al. Among authors: andrade f. Clin Nutr. 2020 Feb;39(2):455-459. doi: 10.1016/j.clnu.2019.02.019. Epub 2019 Feb 15. Clin Nutr. 2020. PMID: 30833214 Free article.
Sanfilippo syndrome: Overall review.
Andrade F, Aldámiz-Echevarría L, Llarena M, Couce ML. Andrade F, et al. Pediatr Int. 2015 Jun;57(3):331-8. doi: 10.1111/ped.12636. Pediatr Int. 2015. PMID: 25851924 Review.
A new metabolic disorder in human cationic amino acid transporter-2 that mimics arginase 1 deficiency in newborn screening.
Yahyaoui R, Blasco-Alonso J, Benito C, Rodríguez-García E, Andrade F, Aldámiz-Echevarría L, Muñoz-Hernández MC, Vega AI, Pérez-Cerdá C, García-Martín ML, Pérez B. Yahyaoui R, et al. Among authors: andrade f. J Inherit Metab Dis. 2019 May;42(3):407-413. doi: 10.1002/jimd.12063. Epub 2019 Feb 21. J Inherit Metab Dis. 2019. PMID: 30671984
New evidence for assessing tetrahydrobiopterin (BH(4)) responsiveness.
Bueno MA, Lage S, Delgado C, Andrade F, Couce ML, González-Lamuño D, Pérez M, Aldámiz-Echevarría L. Bueno MA, et al. Among authors: andrade f. Metabolism. 2012 Dec;61(12):1809-16. doi: 10.1016/j.metabol.2012.07.015. Epub 2012 Aug 24. Metabolism. 2012. PMID: 22921945
1,129 results