Heraldo Mendes Garmes

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

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

Subclinical hypothyroidism in young women with polycystic ovary syndrome: an analysis of clinical, hormonal, and metabolic parameters

Cristina Laguna Benetti‐Pinto, Vanessa Ribeiro Santana Berini Piccolo, Heraldo Mendes Garmes et al. · Fertility and Sterility · 2012 · 106 citations

Metabolic Parameters, Health Sciences, Thyroid Disease +13

Nonsense Mutations in<i>FGF8</i>Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

Ericka Barbosa Trarbach, Ana Paula Abreu, Letícia Ferreira Gontijo Silveira et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 79 citations

Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay

Daiane Beneduzzi, Ericka Barbosa Trarbach, Le Min et al. · Fertility and Sterility · 2014 · 55 citations · Full text

Infertility, Urology, Fertility +12