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

Neonatal lethal hypophosphatasia: A case report and review of literature

por Castells, Laura, Cassanello, Pía, Muñiz, Felix, de Castro, María-José, Couce, María L.
Publicado 2018

Effects of Prebiotic and Probiotic Supplementation on Lactase Deficiency and Lactose Intolerance: A Systematic Review of Controlled Trials

por Leis, Rosaura, de Castro, María-José, de Lamas, Carmela, Picáns, Rosaura, Couce, María L.
Publicado 2020

Evaluation of Body Composition, Physical Activity, and Food Intake in Patients with Inborn Errors of Intermediary Metabolism

por de Castro, María-José, Sánchez-Pintos, Paula, Abdelaziz-Salem, Nisreem, Leis, Rosaura, Couce, María L.
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

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

por Leis, Rosaura, de Lamas, Carmela, de Castro, María-José, Picáns, Rosaura, Gil-Campos, Mercedes, Couce, María L.
Publicado 2019

The LINCE Project: A Pathway for Diagnosing NCL2 Disease

por Rodrigues, Daniel, de Castro, Maria José, Crujeiras, Pablo, Duat-Rodriguez, Anna, Marco, Ana Victoria, del Toro, Mireia, Couce, María L., Colón, Cristóbal
Publicado 2022

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

Carbohydrate status in patients with phenylketonuria

por Couce, María L., Sánchez-Pintos, Paula, Vitoria, Isidro, De Castro, María-José, Aldámiz-Echevarría, Luís, Correcher, Patricia, Fernández-Marmiesse, Ana, Roca, Iria, Hermida, Alvaro, Martínez-Olmos, Miguel, Leis, Rosaura
Publicado 2018

Rapid Molecular Diagnosis of Genetically Inherited Neuromuscular Disorders Using Next-Generation Sequencing Technologies

por Barbosa-Gouveia, Sofia, Vázquez-Mosquera, Maria Eugenia, González-Vioque, Emiliano, Hermida-Ameijeiras, Álvaro, Sánchez-Pintos, Paula, de Castro, Maria José, León, Soraya Ramiro, Gil-Fournier, Belén, Domínguez-González, Cristina, Camacho Salas, Ana, Negrão, Luis, Fineza, Isabel, Laranjeira, Francisco, Couce, Maria Luz
Publicado 2022