ANIBAL
AGUAYO CALCENA
Researcher in the period 2013-2016
Instituto de Investigación Sanitaria Biobizkaia
Barakaldo, EspañaPublications in collaboration with researchers from Instituto de Investigación Sanitaria Biobizkaia (12)
2023
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Autoimmune Diabetes From Childhood to Adulthood: The Role of Pancreatic Autoantibodies and HLA-DRB1 Genotype
The Journal of clinical endocrinology and metabolism, Vol. 108, Núm. 11, pp. e1341-e1346
2021
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Five patients with disorders of calcium metabolism presented with GCM2 gene variants
Scientific Reports, Vol. 11, Núm. 1
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Incidence of diabetes mellitus and associated risk factors in the adult population of the Basque country, Spain
Scientific Reports, Vol. 11, Núm. 1
2020
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Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus
The Journal of clinical endocrinology and metabolism, Vol. 105, Núm. 4
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Novel variant in the CNNM2 gene associated with dominant hypomagnesemia
PLoS ONE, Vol. 15, Núm. 9 September
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Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?
Frontiers in Endocrinology, Vol. 11
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Response to Letter to the Editor: "Forty-One Individuals with Mutations in the AVP-NPII Gene Associated with Familial Neurohypophyseal Diabetes Insipidus
The Journal of clinical endocrinology and metabolism, Vol. 105, Núm. 7
2019
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Variable phenotype in HNF1B mutations: Extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract
Clinical Kidney Journal, Vol. 12, Núm. 3, pp. 373-379
2018
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Identification of a novel large casr deletion in a patient with familial hypocalciuric hypercalcemia
Endocrinology, Diabetes and Metabolism Case Reports, Vol. 2018, Núm. 1, pp. 1-5
2017
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Prevalence of diabetes mellitus and impaired glucose metabolism in the adult population of the Basque Country, Spain
Diabetic Medicine, Vol. 34, Núm. 5, pp. 662-666
2016
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Clinical and genetic characterization of congenital hyperinsulinism in Spain
European Journal of Endocrinology, Vol. 174, Núm. 6, pp. 717-726
2015
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Normal intellectual development in children born from women with hypothyroxinemia during their pregnancy
Journal of Trace Elements in Medicine and Biology, Vol. 31, pp. 18-24