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Medicina Clinica|June 15, 2010
[Neonatal repercussions of immigration in Spain: comparison of periods 2003-2004 and 2007-2008]Antonio Mur Sierra, Fina Díaz, Esperanza Castejón, et al.
Analytical and Bioanalytical Chemistry|May 3, 2014
A capillary electrophoresis procedure for the screening of oligosaccharidoses and related diseasesMercedes Casado, Laura Altimira, Raquel Montero, et al.
Pediatric Neurology|February 5, 2014
Alternating hemiplegia of childhood with a de novo mutation in ATP1A3 and changes in SLC2A1 responsive to a ketogenic dietAdriana Ulate-Campos, Carmen Fons, Rafael Artuch, et al.
Pediatric Neurology|October 18, 2015
Efficacy of the Ketogenic Diet for the Treatment of Refractory Childhood Epilepsy: Cerebrospinal Fluid Neurotransmitters and Amino Acid LevelsAndrea Sariego-Jamardo, Angels García-Cazorla, Rafael Artuch, et al.
Medicina Clinica|February 8, 2011
[Use of illicit drugs over gestation and their neonatal impact. Comparison between periods 1982-1988 and 2002-2008]Sandra Ortigosa Gómez, María Angeles López-Vilchez, Fina Díaz Ledo, et al.
Human Mutation|September 4, 2018
Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlationsDídac Casas-Alba, Antonio Martínez-Monseny, Rosa M Pino-Ramírez, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|June 29, 2016
Hypersensitivity reaction to components of parenteral nutrition in pediatricsCarlos Ruiz Hernández, Esperanza Castejón Ponce, Ferran Bossacoma Busquets, et al.
Human Mutation|January 23, 2014
Two novel mutations in the BCKDK (branched-chain keto-acid dehydrogenase kinase) gene are responsible for a neurobehavioral deficit in two pediatric unrelated patientsAngels García-Cazorla, Alfonso Oyarzabal, Joana Fort, et al.
Orphanet Journal of Rare Diseases|December 1, 2014
Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 casesElena Martín-Hernández, Luis Aldámiz-Echevarría, Esperanza Castejón-Ponce, et al.
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