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JIMD Reports|February 2, 2015
Newborn Screening for Homocystinuria Revealed a High Frequency of MAT I/III Deficiency in Iberian PeninsulaAna Marcão, María L Couce, Célia Nogueira, et al.Nutrients|September 28, 2023
Effects of Maternal Stress on Breast Milk Production and the Microbiota of Very Premature InfantsMaría Del Carmen Fernández-Tuñas, Alejandro Pérez-Muñuzuri, Rocío Trastoy-Pena, et al.Metabolism: Clinical and Experimental|August 28, 2012
New evidence for assessing tetrahydrobiopterin (BH(4)) responsivenessMaría A Bueno, Sergio Lage, Carmen Delgado, et al.Journal of Human Genetics|March 22, 2013
Molecular epidemiology and genotype-phenotype correlation in phenylketonuria patients from South SpainMaría A Bueno, Domingo González-Lamuño, Carmen Delgado-Pecellín, et al.Journal of Human Lactation : Official Journal of International Lactation Consultant Association|January 9, 2020
The Influence of Donor Milk Supplementation on Duration of Parenteral Nutrition in Preterm InfantsBibiana Chinea Jiménez, Marta Cabrera Lafuente, María L Couce, et al.Molecular Genetics and Metabolism|July 1, 2015
Vitamin and mineral status in patients with hyperphenylalaninemiaVanesa Crujeiras, Luis Aldámiz-Echevarría, Jaime Dalmau, et al.Data in Brief|September 1, 2015
Micronutrient in hyperphenylalaninemiaVanesa Crujeiras, Luís Aldámiz-Echevarría, Jaume Dalmau, et al.Molecular Genetics and Metabolism Reports|July 20, 2018
Elosulfase alfa for mucopolysaccharidosis type IVA: Real-world experience in 7 patients from the Spanish Morquio-A early access programGuillem Pintos-Morell, Javier Blasco-Alonso, María L Couce, et al.European Journal of Medical Genetics|July 5, 2014
The early detection of Salla disease through second-tier tests in newborn screening: how to face incidental findingsMaría L Couce, Judit Macías-Vidal, Daisy E Castiñeiras, et al.Frontiers in Pediatrics|April 15, 2022
The LINCE Project: A Pathway for Diagnosing NCL2 DiseaseDaniel Rodrigues, Maria José de Castro, Pablo Crujeiras, et al.Pageof 9