Soara Menabò

Thyrotropin-Stimulating Hormone Receptor Gene Analysis in Pediatric Patients with Non-Autoimmune Subclinical Hypothyroidism

Annalisa Nicoletti, Milva Orquidea Bal, Giuseppina De Marco et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 74 citations

Life Sciences, Endocrinology, Genetics +15

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

Soara Menabò, Seher Polat, Lilia Baldazzi et al. · European Journal of Human Genetics · 2013 · 61 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1

Antonio Balsamo, Alessandro Cicognani, Monia Gennari et al. · European Journal of Endocrinology · 2007 · 24 citations

Medicine, Endocrinology, Genetics +15

Steroid biomarkers for identifying non-classic adrenal hyperplasia due to 21-hydroxylase deficiency in a population of PCOS with suspicious levels of 17OH-progesterone

Claudia Oriolo, Flaminia Fanelli, Silvia Trini Castelli et al. · Journal of Endocrinological Investigation · 2020 · 19 citations

Life Sciences, Endocrinology, Gynecology +15

A sequence variation in 3'UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia.

Soara Menabò, Antonio Balsamo, Lilia Baldazzi et al. · PubMed · 2012 · 17 citations

Medicine, Genetics, Molecular Genetics +10