Beatriz R. Versiani

Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome

Ana Paula Abreu, Ericka Barbosa Trarbach, Margaret de Castro et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 120 citations · Full text

Medicine, Endocrinology, Genetics +17

Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism with and without Anosmia

Ericka Barbosa Trarbach, Elaine Maria Frade Costa, Beatriz R. Versiani et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 108 citations · Full text

Life Sciences, Endocrinology, Genetics +14

Quantitative Magnetic Resonance Imaging Evaluation of the Olfactory System in Kallmann Syndrome: Correlation with a Clinical Smell Test

Marcel Koenigkam Santos, Antônio Carlos Santos, Beatriz R. Versiani et al. · Neuroendocrinology · 2011 · 48 citations · Full text

Medicine, Neurology, Radiology +17

Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes

Beatriz R. Versiani, Enid Gilbert‐Barness, Liane R. Giuliani et al. · Clinical Dysmorphology · 2003 · 32 citations

Medicine, Endocrinology, Obstetrics +17

Clinical assessment and molecular analysis of <i>GnRHR</i> and <i>KAL1</i> genes in males with idiopathic hypogonadotrophic hypogonadism

Beatriz R. Versiani, Ericka Barbosa Trarbach, Marcel Koenigkam Santos et al. · Clinical Endocrinology · 2006 · 26 citations

Medicine, Endocrinology, Genetics +15