Publicacións nas que colabora con María Luz Couce Pico (46)
2017
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Hepatic damage and glutamate oxaloacetate transaminase elevations during fetal asphyxia
Developmental Medicine and Child Neurology
2016
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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
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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
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A rare cause of neonatal obstructive jaundice
Gastroenterology
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Corrigendum to "A glimpse into past, present, and future DNA sequencing" [Mol. Genet. Metab. 110 (2013) 3-24]
Molecular Genetics and Metabolism
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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
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Corrigendum to "Risk factors for developing mineral bone disease in phenylketonuric patients" [Mol. Genet. Metab. 108 (2013) 149-154]
Molecular Genetics and Metabolism
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Effects of different arachidonic acid supplementation on psychomotor development in very preterm infants; A randomized controlled trial
Nutrition Journal, Vol. 14, Núm. 1
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New insights in growth of phenylketonuric patients
European Journal of Pediatrics, Vol. 174, Núm. 5, pp. 651-659
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Newborn screening for homocystinuria revealed a high frequency of MAT I/III deficiency in iberian Peninsula
JIMD Reports (Springer), pp. 113-120
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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
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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
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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
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Cribado neonatal
Tratado de pediatría (Editorial Médica Panamericana), pp. 138-142
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Parálisis de cuerda vocal izquierda como complicación de la cirugía del ductus arterioso persistente
Anales de Pediatria, Vol. 82, Núm. 1, pp. e7-e11
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Preclinical screening for retinopathy of prematurity risk using IGF1 levels at 3 weeks post-partum
PLoS ONE, Vol. 9, Núm. 2
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Prenatal alcohol exposure and its repercussion on newborns
Journal of Neonatal-Perinatal Medicine, Vol. 7, Núm. 1, pp. 47-54
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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
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Utilidad de la distracción mandibular en la secuencia de Pierre Robin en el período neonatal
Anales de Pediatria
2013
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A glimpse into past, present, and future DNA sequencing
Molecular Genetics and Metabolism, Vol. 110, Núm. 1-2, pp. 3-24