Clin. Endocrinol. (Oxf)

Identification of autoimmune polyendocrine syndrome type 1 in patients with isolated hypoparathyroidism.

Sahoo SK, Zaidi G, Srivastava R, ..., Aggarwal R, Bhatia E

Clin. Endocrinol. (Oxf) 85 (4) 544-550 [2016-10-00; online 2016-06-28]

Affiliated researcher

In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia.

Barbaro M, Soardi FC, Östberg LJ, ..., Wedell A, Lajic S

Clin. Endocrinol. (Oxf) 82 (1) 37-44 [2015-01-00; online 2014-07-07]

Affiliated researcher