Bone Mineralization and Calcium Phosphorus Metabolism

por Couce, María Luz, Saenz de Pipaon, Miguel
Publicado 2021

Effects of LC-PUFA Supplementation in Patients with Phenylketonuria: A Systematic Review of Controlled Trials

por Couce, María Luz, de Castro, María José, de Lamas, Carmela, Leis, Rosaura
Publicado 2019

Gene Therapy for Neuronopathic Mucopolysaccharidoses: State of the Art

por de Castro, María José, del Toro, Mireia, Giugliani, Roberto, Couce, María Luz
Publicado 2021

Umbilical cord and visceral hemangiomas diagnosed in the neonatal period: A case report and a review of the literature

por Iglesias-Deus, Alicia, Pérez-Muñuzuri, Alejandro, Urisarri, Adela, Bautista-Casasnovas, Adolfo, Couce, Maria-Luz
Publicado 2016

Arterial stiffness assessment in patients with phenylketonuria

por Hermida-Ameijeiras, Alvaro, Crujeiras, Vanesa, Roca, Iria, Calvo, Carlos, Leis, Rosaura, Couce, María-Luz
Publicado 2017

Breastfeeding and Inborn Errors of Amino Acid and Protein Metabolism: A Spreadsheet to Calculate Optimal Intake of Human Milk and Disease-Specific Formulas

por Vitoria-Miñana, Isidro, Couce, María-Luz, González-Lamuño, Domingo, García-Peris, Mónica, Correcher-Medina, Patricia
Publicado 2023

Case Report: Diffuse Polymicrogyria Associated With a Novel ADGRG1 Variant

por Carneiro, Fábio, Duarte, Júlia, Laranjeira, Francisco, Barbosa-Gouveia, Sofia, Couce, María-Luz, Fonseca, Maria José
Publicado 2021

Trace elements in dried blood spots as potential discriminating features for metabolic disorder diagnosis in newborns

por Moreda-Piñeiro, Jorge, Cocho, José A, Couce, María Luz, Moreda-Piñeiro, Antonio, Bermejo-Barrera, Pilar
Publicado 2021

Similarities between acylcarnitine profiles in large for gestational age newborns and obesity

por Sánchez-Pintos, Paula, de Castro, Maria-Jose, Roca, Iria, Rite, Segundo, López, Miguel, Couce, Maria-Luz
Publicado 2017

Bone Status in Patients with Phenylketonuria: A Systematic Review

por de Castro, María José, de Lamas, Carmela, Sánchez-Pintos, Paula, González-Lamuño, Domingo, Couce, María Luz
Publicado 2020

Congenital intestinal atresias with multiple episodes of sepsis: A case report and review of literature

por Mandiá, Natalia, Pérez-Muñuzuri, Alejandro, López-Suárez, Olalla, López-Sanguos, Carolina, Bautista-Casanovas, Adolfo, Couce, Mariá-Luz
Publicado 2018

Retrospective study to identify risk factors for chronic kidney disease in children with congenital solitary functioning kidney detected by neonatal renal ultrasound screening

por Urisarri, Adela, Gil, Marta, Mandiá, Natalia, Aldamiz-Echevarría, Luís, Iria, Roca, González-Lamuño, Domingo, Couce, María-Luz
Publicado 2018

Screen Time and Bone Status in Children and Adolescents: A Systematic Review

por de Lamas, Carmela, Sánchez-Pintos, Paula, José de Castro, María, Sáenz de Pipaon, Miguel, Couce, María Luz
Publicado 2021

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

por Pérez-Muñuzuri, Alejandro, López-Suárez, Olalla, Mandiá-Rodríguez, Natalia, López-Sanguos, Carolina, Blanco-Teijeiro, María José, Couce, María Luz
Publicado 2020

Clinical manifestations in female carriers of mucopolysaccharidosis type II: a spanish cross-sectional study

por Guillén-Navarro, Encarna, Domingo-Jiménez, María Rosario, Alcalde-Martín, Carlos, Cancho-Candela, Ramón, Couce, María Luz, Galán-Gómez, Enrique, Alonso-Luengo, Olga
Publicado 2013

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

por de Castro, María José, González-Vioque, Emiliano, Barbosa-Gouveia, Sofía, Salguero, Enrique, Rite, Segundo, López-Suárez, Olalla, Pérez-Muñuzuri, Alejandro, Couce, María-Luz
Publicado 2020

A selective screening program for the early detection of mucopolysaccharidosis: Results of the FIND project – a 2-year follow-up study

por Colón, Cristóbal, Alvarez, J. Victor, Castaño, Cristina, Gutierrez-Solana, Luís G., Marquez, Ana M., O’Callaghan, María, Sánchez-Valverde, Félix, Yeste, Carmen, Couce, María-Luz
Publicado 2017

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

por Barbosa-Gouveia, Sofia, González-Vioque, Emiliano, Borges, Filipa, Gutiérrez-Solana, Luis, Wintjes, Liesbeth, Kappen, Antonia, van den Heuvel, Lambert, Leis, Rosaura, Rodenburg, Richard, Couce, María Luz
Publicado 2019

Identification of a Novel Variant in EARS2 Associated with a Severe Clinical Phenotype Expands the Clinical Spectrum of LTBL

por Barbosa-Gouveia, Sofia, González-Vioque, Emiliano, Hermida, Álvaro, Suarez, María Unceta, Martínez-González, María Jesús, Borges, Filipa, Wintjes, Liesbeth, Kappen, Antonia, Rodenburg, Richard, Couce, María-Luz
Publicado 2020

Oral Administration to Nursing Women of Lactobacillus fermentum CECT5716 Prevents Lactational Mastitis Development: A Randomized Controlled Trial

por Hurtado, José A., Maldonado-Lobón, Jose A., Díaz-Ropero, M. Paz, Flores-Rojas, Katherine, Uberos, José, Leante, José L., Affumicato, Laura, Couce, María Luz, Garrido, José M., Olivares, Mónica, Fonollá, Juristo
Publicado 2017