Guilherme Guaragna‐Filho

Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3

Delanie B. Macedo, Ana Paula Abreu, Ana Claudia S. Reis et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 138 citations · Full text

Medicine, Genetics, Molecular Genetics +17

The Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor Gene

Angela Lucas-Herald, Silvano Bertelloni, Anders Juul et al. · The Journal of Clinical Endocrinology & Metabolism · 2016 · 111 citations · Full text

Medicine, Endocrinology, Genetics +17

408 Cases of Genital Ambiguity Followed by Single Multidisciplinary Team during 23 Years: Etiologic Diagnosis and Sex of Rearing

Georgette B. Paula, Beatriz Amstalden Barros, Stela Carpini et al. · International Journal of Endocrinology · 2016 · 40 citations · Full text

Medicine, Genetics, Gynecology +17

Real-World Estimates of Adrenal Insufficiency–Related Adverse Events in Children With Congenital Adrenal Hyperplasia

Salma Ali, Jillian Bryce, Houra Haghpanahan et al. · The Journal of Clinical Endocrinology & Metabolism · 2020 · 40 citations · Full text

Medicine, Endocrinology, Pediatrics +10

Clinical and molecular spectrum of patients with 17β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency

Carla Cristina Telles de Sousa Castro, Guilherme Guaragna‐Filho, Flávia Leme de Calais et al. · Arquivos Brasileiros de Endocrinologia & Metabologia · 2012 · 37 citations · Full text

Life Sciences, Endocrinology, Genetics +17