Grupo de Investigación en Endocrinología, Diabetes, Nutrición,Alteraciones Renales y Salud Infantil
Instituto de Salud Carlos III
Madrid, EspañaPublicaciones en colaboración con investigadoras/es de Instituto de Salud Carlos III (20)
2021
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Fatty liver index as a predictor for type 2 diabetes in subjects with normoglycemia in a nationwide cohort study
Scientific Reports, Vol. 11, Núm. 1
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Iodine Deficiency and Mortality in Spanish Adults: Di@bet.es Study
Thyroid, Vol. 31, Núm. 1, pp. 106-114
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Thyroid hormone resistance index and mortality in euthyroid subjects: Di@bet.es study
European journal of endocrinology, Vol. 186, Núm. 1, pp. 95-103
2020
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Incidence and regression of metabolic syndrome in a representative sample of the Spanish population: Results of the cohort di@bet.es study
BMJ Open Diabetes Research and Care, Vol. 8, Núm. 1
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Incidence of diabetes mellitus in Spain as results of the nation-wide cohort di@bet.es study
Scientific Reports, Vol. 10, Núm. 1
2019
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Ambient temperature and prevalence of diabetes and insulin resistance in the Spanish population: Di@bet.es study
European Journal of Endocrinology, Vol. 180, Núm. 5, pp. 275-282
2018
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Iron deficiency is associated with Hypothyroxinemia and Hypotriiodothyroninemia in the Spanish general adult population: Di@bet.es study
Scientific Reports, Vol. 8, Núm. 1
2017
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Osteopontin regulates the cross-talk between phosphatidylcholine and cholesterol metabolism in mouse liver
Journal of Lipid Research, Vol. 58, Núm. 9, pp. 1903-1915
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Population-Based National Prevalence of Thyroid Dysfunction in Spain and Associated Factors: Study
Thyroid, Vol. 27, Núm. 2, pp. 156-166
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Reference values for TSH may be inadequate to define hypothyroidism in persons with morbid obesity: Di@bet.es study
Obesity, Vol. 25, Núm. 4, pp. 788-793
2016
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A Novel Mutation in a Patient with Hyperparathyroidism–Jaw Tumour Syndrome
Endocrine Pathology, Vol. 27, Núm. 2, pp. 142-146
2013
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Endocrine profile and phenotype-(Epi)genotype correlation in Spanish patients with pseudohypoparathyroidism
Journal of Clinical Endocrinology and Metabolism, Vol. 98, Núm. 5
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Factors determining high-sensitivity C-reactive protein values in the Spanish population. Di@bet.es study
European Journal of Clinical Investigation, Vol. 43, Núm. 1, pp. 1-10
2012
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Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locus
Journal of Clinical Endocrinology and Metabolism, Vol. 97, Núm. 6
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Permanent neonatal diabetes caused by creation of an ectopic splice site within the INS gene
PLoS ONE, Vol. 7, Núm. 1
2010
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Neonatal diabetes caused by mutations in sulfonylurea receptor 1: Interplay between expression and Mg-nucleotide gating defects of ATP-sensitive potassium channels
Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 12
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Novel (60%) and recurrent (40%) androgen receptor gene mutations in a series of 59 patients with a 46,XY disorder of sex development
Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 4, pp. 1876-1888
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Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis
Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Núm. 7, pp. 3105-3110
2009
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Two cases of deletion 2q37 associated with segregation of an unbalanced translocation 2;21: Choanal atresia leading to misdiagnosis of CHARGE syndrome
European Journal of Endocrinology, Vol. 160, Núm. 4, pp. 711-717
1995
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Factors influencing the immediate and late outcome of Cushing's disease treated by transsphenoidal surgery: A retrospective study by the European Cushing's Disease Survey Group
Journal of Clinical Endocrinology and Metabolism, Vol. 80, Núm. 11, pp. 3114-3120