Lidia
Castro Feijoo
Publicacións (29) Publicacións de Lidia Castro Feijoo
2023
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Cost-effectiveness of somatrogon in the Spanish pediatric population with growth hormone deficiency
Expert Review of Pharmacoeconomics and Outcomes Research, Vol. 23, Núm. 10, pp. 1139-1146
2019
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Hipocrecimiento armónico
Manual de pediatría (Ergon), pp. 726-732
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Hipopituitarismo
Manual de pediatría (Ergon), pp. 748-754
2018
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Congenital hyperinsulinism in two siblings with ABCC8 mutation: Same genotype, different phenotypes
Archives of Endocrinology and Metabolism, Vol. 62, Núm. 5, pp. 560-565
2017
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Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 gene
Hormones, Vol. 16, Núm. 2, pp. 194-199
2016
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Changes in body mass index in girls with idiopathic central precocious puberty under gonadotropin-releasing hormone analogue therapy: The Spanish registry
Hormone Research in Paediatrics, Vol. 86, Núm. 3, pp. 154-160
2015
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Precocious presentation of autoimmune polyglandular syndrome type 2 associated with an AIRE mutation
Hormones, Vol. 14, Núm. 2, pp. 312-316
2014
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Hiperpituitarismo
Tratado de pediatría (Editorial Médica Panamericana), pp. 1238-1243
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Hipopituitarismo
Tratado de pediatría (Editorial Médica Panamericana), pp. 1213-1223
2011
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Congenital hypothyroidism with neurological and respiratory alterations: A case detected using a variable diagnostic threshold for Tsh
JCRPE Journal of Clinical Research in Pediatric Endocrinology, Vol. 3, Núm. 4, pp. 208-211
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Evolutionary analyses of entire genomes do not support the association of mtdna mutations with ras/mapk pathway syndromes
PLoS ONE, Vol. 6, Núm. 4
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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 type
BMC Medical Genetics, Vol. 12
2010
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Central precocious puberty in children living in Spain: Incidence, prevalence, and influence of adoption and immigration
Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 9, pp. 4305-4313
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Functional consequences of seven novel mutations in the CYP11B1 gene: Four mutations associated with nonclassic and three mutations causing classic 11β-hydroxylase deficiency
Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 2, pp. 779-788
2008
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Hypochondroplasia and acanthosis nigricans: A new syndrome due to the p.Lys650Thr mutation in the fibroblast growth factor receptor 3 gene?
European Journal of Endocrinology, Vol. 159, Núm. 3, pp. 243-249
2007
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Hipoglucemia neonatal
Anales de Pediatria
2006
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Pubertad precoz
Anales de Pediatria Continuada, Vol. 4, Núm. 2, pp. 79-87
2005
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Endocrine Disruptors
Journal of Pediatric Endocrinology and Metabolism, Vol. 18, pp. 1145-1156
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Genetic basis of short stature
Journal of Endocrinological Investigation
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Kallmann's syndrome with a novel missense mutation in the KAL1 gene that modifies the major cell adhesion site of the anosmin-1 protein
Journal of Pediatric Endocrinology and Metabolism, Vol. 18, Núm. 6, pp. 545-548