MARIA DE LA LUZ
COUCE PICO
Profesora titular de universidade
Hospital Universitario La Paz
Madrid, EspañaPublikationen in Zusammenarbeit mit Forschern von Hospital Universitario La Paz (24)
2024
2021
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Bone mineral density, body composition, and metabolic health of very low birth weight infants fed in hospital following current macronutrient recommendations during the first 3 years of life
Nutrients, Vol. 13, Núm. 3, pp. 1-20
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Bone mineralization and calcium phosphorus metabolism
Nutrients
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Extremely Preterm Infant Admissions Within the SafeBoosC-III Consortium During the COVID-19 Lockdown
Frontiers in Pediatrics, Vol. 9
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Recommendations on the skills profile and standards of the neonatal transport system in Spain
Anales de Pediatria, Vol. 94, Núm. 6, pp. 420.e1-420.e11
2020
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Incidence, Treatment, and Outcome Trends of Necrotizing Enterocolitis in Preterm Infants: A Multicenter Cohort Study
Frontiers in Pediatrics, Vol. 8
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Prevention, diagnosis and treatment of necrotising enterocolitis in newborns less than 32 weeks at birth in Spain
Anales de Pediatria, Vol. 93, Núm. 3, pp. 161-169
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The Influence of Donor Milk Supplementation on Duration of Parenteral Nutrition in Preterm Infants
Journal of Human Lactation, Vol. 36, Núm. 2, pp. 245-253
2019
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Clinical and molecular diagnosis of non-phosphomannomutase 2 N-linked congenital disorders of glycosylation in Spain
Clinical Genetics, Vol. 95, Núm. 5, pp. 615-626
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Cohort study showed that growth rate increment has not been enough to prevent growth retardation of preterm infants and raised concerns about unbalanced growth
Acta Paediatrica, International Journal of Paediatrics, Vol. 108, Núm. 10, pp. 1793-1800
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Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain
Medicine (United States), Vol. 98, Núm. 39
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The Effect of Morbidity and Sex on Postnatal Growth of Very Preterm Infants: A Multicenter Cohort Study
Neonatology, Vol. 115, Núm. 4, pp. 348-354
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The impact of postnatal systemic steroids on the growth of preterm infants: A multicenter cohort study
Nutrients, Vol. 11, Núm. 11
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Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program
European Journal of Human Genetics, Vol. 27, Núm. 4, pp. 556-562
2018
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Clinical Assessment of Dysarthria in Children with Cerebellar Syndrome Associated with PMM2-CDG
Neuropediatrics, Vol. 49, Núm. 6, pp. 408-413
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Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variants
Orphanet Journal of Rare Diseases, Vol. 13, Núm. 1
2017
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A quantitative assessment of the evolution of cerebellar syndrome in children with phosphomannomutase-deficiency (PMM2-CDG)
Orphanet Journal of Rare Diseases, Vol. 12, Núm. 1
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Clinical and genetic features of 13 Spanish patients with KCNQ2 mutations
Journal of Human Genetics, Vol. 62, Núm. 2, pp. 185-189
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Infantile-onset Pompe disease with neonatal debut: A case report and literature review
Medicine (United States), Vol. 96, Núm. 51
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¿Cuál es la nutrición que administramos a nuestros recién nacidos de muy bajo peso en las unidades neonatales?: Una encuesta nacional
Nutricion Hospitalaria, Vol. 34, Núm. 5, pp. 1067-1072