Publicacións nas que colabora con María Luz Couce Pico (46)

2017

  1. Hepatic damage and glutamate oxaloacetate transaminase elevations during fetal asphyxia

    Developmental Medicine and Child Neurology

2016

  1. Evaluation of carnitine deficit in very low birth weight preterm newborns small for their gestational age

    Journal of Maternal-Fetal and Neonatal Medicine, Vol. 29, Núm. 6, pp. 933-937

  2. Potential protective role of endogenous glutamate-oxaloacetate transaminase against glutamate excitotoxicity in fetal hypoxic-ischaemic asphyxia

    Developmental Medicine and Child Neurology, Vol. 58, Núm. 1, pp. 57-62

2015

  1. A rare cause of neonatal obstructive jaundice

    Gastroenterology

  2. Corrigendum to "A glimpse into past, present, and future DNA sequencing" [Mol. Genet. Metab. 110 (2013) 3-24]

    Molecular Genetics and Metabolism

  3. Corrigendum to "Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening" [Mol. Genet. Metab. 110 (2013) 218-221]

    Molecular Genetics and Metabolism

  4. Corrigendum to "Risk factors for developing mineral bone disease in phenylketonuric patients" [Mol. Genet. Metab. 108 (2013) 149-154]

    Molecular Genetics and Metabolism

  5. Effects of different arachidonic acid supplementation on psychomotor development in very preterm infants; A randomized controlled trial

    Nutrition Journal, Vol. 14, Núm. 1

  6. New insights in growth of phenylketonuric patients

    European Journal of Pediatrics, Vol. 174, Núm. 5, pp. 651-659

  7. Newborn screening for homocystinuria revealed a high frequency of MAT I/III deficiency in iberian Peninsula

    JIMD Reports (Springer), pp. 113-120

  8. Percentiles de carnitina y acilcarnitinas en muestras de cribado neonatal de prematuros de muy bajo peso

    Anales de Pediatría: Publicación Oficial de la Asociación Española de Pediatría ( AEP ), Vol. 82, Núm. 4, pp. 285-287

  9. Utilidad de los marcadores de remodelado óseo en la detección de enfermedad mineral ósea en pacientes con fenilcetonuria

    Medicina Clinica, Vol. 144, Núm. 5, pp. 193-197

2014

  1. Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders

    Orphanet Journal of Rare Diseases, Vol. 9, Núm. 1

  2. Cribado neonatal

    Tratado de pediatría (Editorial Médica Panamericana), pp. 138-142

  3. Parálisis de cuerda vocal izquierda como complicación de la cirugía del ductus arterioso persistente

    Anales de Pediatria, Vol. 82, Núm. 1, pp. e7-e11

  4. Preclinical screening for retinopathy of prematurity risk using IGF1 levels at 3 weeks post-partum

    PLoS ONE, Vol. 9, Núm. 2

  5. Prenatal alcohol exposure and its repercussion on newborns

    Journal of Neonatal-Perinatal Medicine, Vol. 7, Núm. 1, pp. 47-54

  6. The early detection of Salla disease through second-tier tests in newborn screening: How to face incidental findings

    European Journal of Medical Genetics, Vol. 57, Núm. 9, pp. 527-531

  7. Utilidad de la distracción mandibular en la secuencia de Pierre Robin en el período neonatal

    Anales de Pediatria

2013

  1. A glimpse into past, present, and future DNA sequencing

    Molecular Genetics and Metabolism, Vol. 110, Núm. 1-2, pp. 3-24