Publicaciones en colaboración con investigadores/as de Instituto de Salud Carlos III (6)

2022

  1. Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry

    Clinical Endocrinology, Vol. 97, Núm. 5, pp. 551-561

2021

  1. Phenotypic Variability of Patients With PAX8 Variants Presenting With Congenital Hypothyroidism and Eutopic Thyroid

    The Journal of clinical endocrinology and metabolism, Vol. 106, Núm. 1, pp. e152-e170

  2. Ultrasound criteria (EU-TIRADS) to identify thyroid nodule malignancy risk in adolescents. Correlation with cyto-histological findings

    Endocrinologia, Diabetes y Nutricion, Vol. 68, Núm. 10, pp. 728-734

2018

  1. Building a theoretical framework for autism spectrum disorders screening instruments in Europe

    Child and Adolescent Mental Health, Vol. 23, Núm. 4, pp. 359-367

2011

  1. SRD5A2 gene mutations and polymorphisms in Spanish 46,XY patients with a disorder of sex differentiation

    International Journal of Andrology, Vol. 34, Núm. 6 PART 2

2010

  1. 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