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The Journal of Clinical Endocrinology and Metabolism|June 18, 2010
Central precocious puberty in children living in Spain: incidence, prevalence, and influence of adoption and immigrationLeandro Soriano-Guillén, Raquel Corripio, José Ignacio Labarta, et al.
Frontiers in Endocrinology|December 22, 2025
Delphi-based Spanish consensus on the use of long-acting growth hormone in pediatric growth hormone deficiency: recommendations from the ConverGHe Working GroupLidia Castro-Feijóo, José-Ignacio Labarta-Aizpún, Marta Ramon-Krauel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 27, 2005
Kallmann's syndrome with a novel missense mutation in the KAL1 gene that modifies the major cell adhesion site of the anosmin-1 proteinLourdes Loidi, Lidia Castro-Feijóo, Jesús Barreiro, et al.
European Journal of Endocrinology|June 28, 2008
Hypochondroplasia and Acanthosis nigricans: a new syndrome due to the p.Lys650Thr mutation in the fibroblast growth factor receptor 3 gene?Lidia Castro-Feijóo, Lourdes Loidi, Anxo Vidal, et al.
Hormones (Athens, Greece)|July 26, 2017
Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 geneTeresa Rego, Carmen Gomez Lado, Paloma Cabanas Rodríguez, et al.
Archives of Endocrinology and Metabolism|November 22, 2018
Congenital hyperinsulinism in two siblings with ABCC8 mutation: same genotype, different phenotypesFrancisco Sousa-Santos, Helder Simões, Lidia Castro-Feijóo, et al.
Plos One|April 29, 2011
Evolutionary analyses of entire genomes do not support the association of mtDNA mutations with Ras/MAPK pathway syndromesAlberto Gómez-Carballa, María Cerezo, Emilia Balboa, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiencySilvia Parajes, Lourdes Loidi, Nicole Reisch, et al.
BMC Medical Genetics|September 10, 2011
Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation typeMarcos Morey, Lidia Castro-Feijóo, Jesús Barreiro, et al.
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