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Best Practice & Research. Clinical Endocrinology & Metabolism|November 19, 2021
Genetics of ovarian insufficiency and defects of folliculogenesisMonica Malheiros França, Berenice Bilharinho Mendonca
Journal of the Endocrine Society|February 27, 2020
Genetics of Primary Ovarian Insufficiency in the Next-Generation Sequencing EraMonica Malheiros França, Berenice Bilharinho Mendonca
The Application of Clinical Genetics|April 30, 2020
Integrative and Analytical Review of the 5-Alpha-Reductase Type 2 Deficiency WorldwideRafael Loch Batista, Berenice Bilharinho Mendonca
Arquivos Brasileiros De Endocrinologia E Metabologia|May 17, 2014
Clinical management of transsexual subjectsElaine Maria Frade Costa, Berenice Bilharinho Mendonca
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|June 6, 2022
Mild Androgen Insensitivity Syndrome: The Current LandscapeRafael Loch Batista, Flora Ladeira Craveiro, Raquel Martinez Ramos, et al.
Clinical Endocrinology|September 25, 2008
46,XY disorders of sex development (DSD)Berenice Bilharinho Mendonca, Sorahia Domenice, Ivo J P Arnhold, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 9, 2006
Preclinical diagnosis of testotoxicosis in a boy with an activating mutation of the luteinizing hormone receptorMilena Teles, Vinicius Nahime Brito, Ivo Jorge Prado Arnhold, et al.
Hormone Research in Paediatrics|August 12, 2010
The role of SRY mutations in the etiology of gonadal dysgenesis in patients with 45,X/46,XY disorder of sex development and variantsMirian Yumie Nishi, Elaine Maria Frade Costa, Suely Beirão Oliveira, et al.
Clinics (Sao Paulo, Brazil)|August 11, 2024
Development and validation of a liquid chromatography coupled to a diode array detector (LC-DAD) method for measuring mitotane (DDD) in plasma samplesAnna Sylvia Ferrari Marques, Atecla Nunciata Lopes Alves, Berenice Bilharinho Mendonca, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levelsMariana Tenorio Antunes Reis, Andreina Cattani, Berenice Bilharinho Mendonca, et al.
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