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Clinical Utility of LCT Genotyping in Children with Suspected Functional Gastrointestinal Disorder

2020- Couce Pico, María Luz; Sánchez Pintos, Paula; González Vioque, Emiliano; Leis Trabazo, María Rosaura

Rapid Phenotype-Driven Gene Sequencing with the NeoSeq Panel: A Diagnostic Tool for Critically Ill Newborns with Suspected Genetic Disease

2020- De Castro López, María José; González Vioque, Emiliano; Barbosa Gouveia, Sofía; Salguero, E.; Rite, S.; [et al.]

Incidence, Treatment, and Outcome Trends of Necrotizing Enterocolitis in Preterm Infants: A Multicenter Cohort Study

2020- Zozaya, Carlos; García González, Inés; Ávila Álvarez, Alejandro; Oikonomopoulou, Niki; Sánchez Tamayo, Tomás; [et al.]

Validation of an IGF1 Screening Method for Retinopathy of Pre-maturity

2020- Pérez Muñuzuri, Alejandro; López Suárez, Olalla Elena; Mandía Rodríguez, Natalia; López Sanguos, Carolina; Blanco Teijeiro, María Jose; [et al.]

Characterization of New Proteomic Biomarker Candidates in Mucopolysaccharidosis Type IVA

2020- Álvarez, V. J.; Bravo López, Susana Belén; Chantada Vázquez, María Pilar; Colón Mejeras, Cristobal; De Castro López, María José; [et al.]

Bone Status in Patients with Phenylketonuria: A Systematic Review

2020- De Castro López, María José; de Lamas, C.; Sánchez Pintos, Paula; González-Lamuño, D.; Couce Pico, María Luz

Mucopolysaccharidosis IVA: Diagnosis, Treatment, and Management

2020- Sawamoto, K.; Gonzalez, J. V. A.; Piechnik, M.; Otero, F. J.; Couce Pico, María Luz; [et al.]

Trends in Outcomes for Neonates Born Very Preterm and Very Low Birth Weight in 11 High-Income Countries

2019- Lui, K.; Lee, S. K.; Kusuda, S.; Adams, M.; Vento, M.; [et al.]

Effect of allopurinol in addition to hypothermia treatment in neonates for hypoxic-ischemic brain injury on neurocognitive outcome (ALBINO): study protocol of a blinded randomized placebo-controlled parallel group multicenter trial for superiority (phase III)

2019- Maiwald, C. A.; Annink, K. V.; Rudiger, M.; Benders, Mjnl; van Bel, F.; [et al.]

Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program

2019- Navarrete, R.; Leal, F.; Vega, A. I.; Morais-López, A.; Garcia-Silva, M. T.; [et al.]

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