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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.]

Proteomic analysis in morquio a cells treated with immobilized enzymatic replacement therapy on nanostructured lipid systems

2019- Álvarez González, José Victor; Bravo López, Susana Belén; García-Vence, M.; De Castro López, María José; Luzardo, A.; [et al.]

The impact of postnatal systemic steroids on the growth of preterm infants: A multicenter cohort study

2019- Zozaya, C.; Avila-Alvarez, A.; Rodrigo, F. G. M.; Couce Pico, María Luz; Arruza, L.; [et al.]

Effects of Nutritional Education Interventions on Metabolic Risk in Children and Adolescents: A Systematic Review of Controlled Trials

2019- Leis Trabazo, María Rosaura; de Lamas, C.; De Castro López, María José; Picáns, R.; Gil-Campos, M.; [et al.]

Acylcarnitine profile in neonatal hypoxic-ischemic encephalopathy: The value of butyrylcarnitine as a prognostic marker

2019- López Suárez, Olalla Elena; CONCHEIRO GUISAN, ANA; Sánchez Pintos, Paula; Cocho, J. A.; FERNANDEZ LORENZO, JOSE RAMON; [et al.]

Betaine anhydrous in homocystinuria: results from the RoCH registry

2019- Valayannopoulos, V.; Schiff, M.; Guffon, N.; Nadjar, Y.; García-Cazorla, A.; [et al.]

The natural history of classic galactosemia: lessons from the GalNet registry

2019- Rubio-Gozalbo, M. E.; Haskovic, M.; Bosch, A. M.; Burnyte, B.; Coelho, A. I.; [et al.]

Identification and Characterization of New Variants in FOXRED1 Gene Expands the Clinical Spectrum Associated with Mitochondrial Complex I Deficiency

2019- Barbosa Gouveia, Sofía; González Vioque, Emiliano; Borges ., Filipa; Gutiérrez-Solana, L.; Wintjes, L.; [et al.]

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