José Ignacio Labarta Aizpun-rekin lankidetzan egindako argitalpenak (4)

2017

  1. Recommendations for the diagnosis and treatment of classic forms of 21-hydroxylase-deficient congenital adrenal hyperplasia

    Anales de Pediatria, Vol. 87, Núm. 2, pp. 116.e1-116.e10

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

2009

  1. Longitudinal pubertal growth according to age at pubertal growth spurt onset: Data from a Spanish study including 458 children (223 boys and 235 girls)

    Journal of Pediatric Endocrinology and Metabolism, Vol. 22, Núm. 8, pp. 715-726

2006

  1. Exon 3-deleted/full-length growth hormone receptor polymorphism genotype frequencies in Spanish short small-for-gestational-age (SGA) children and adolescents (n = 247) and in an adult control population (n = 289) show increased fl/fl in short SGA

    Journal of Clinical Endocrinology and Metabolism, Vol. 91, Núm. 12, pp. 5038-5043