Grupo de Investigación en Endocrinología, Diabetes, Nutrición,Alteraciones Renales y Salud Infantil
Hospital Universitario La Paz
Madrid, EspañaPublicaciones en colaboración con investigadoras/es de Hospital Universitario La Paz (13)
2023
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Mortality in Acromegaly Diagnosed in Older Individuals in Spain Is Higher in Women Compared to the General Spanish Population
The Journal of clinical endocrinology and metabolism, Vol. 108, Núm. 9, pp. 2193-2202
2022
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Consensus guide on prophylactic gonadectomy in different sex development
Endocrinologia, Diabetes y Nutricion, Vol. 69, Núm. 8, pp. 629-645
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Factors associated with therapeutic response in acromegaly diagnosed in the elderly in Spain
Frontiers in Endocrinology, Vol. 13
2021
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Craniopharyngioma in the Elderly: A Multicenter and Nationwide Study in Spain
Neuroendocrinology, Vol. 111, Núm. 10, pp. 925-936
2013
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Changes in acromegaly treatment over four decades in Spain: Analysis of the Spanish Acromegaly Registry (REA)
Pituitary, Vol. 16, Núm. 1, pp. 115-121
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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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Genetics of Type III Bartter Syndrome in Spain, Proposed Diagnostic Algorithm
PLoS ONE, Vol. 8, Núm. 9
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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Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individuals
Journal of Clinical Endocrinology and Metabolism, Vol. 97, Núm. 7
2011
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Estudio OASIS: Manejo terapéutico de la acromegalia en un escenario de práctica clínica habitual. Evaluación de la eficacia de las diversas estrategias de tratamiento aplicadas
Endocrinologia y Nutricion, Vol. 58, Núm. 9, pp. 478-486
2010
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Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and GNAS imprinting defects
Journal of Medical Genetics, Vol. 47, Núm. 4, pp. 276-280
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New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism
European Journal of Endocrinology, Vol. 163, Núm. 6, pp. 953-962
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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