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Molecular and Cellular Endocrinology|June 14, 2011
New genetic factors implicated in human GnRH-dependent precocious puberty: the role of kisspeptin systemMilena Gurgel Teles, Leticia Ferreira Gontijo Silveira, Cintia Tusset, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|January 31, 2006
[Endocrine tumors associated to protein Gsalpha/Gi2alpha mutations]Milena Gurgel Teles Bezerra, Ana Claudia Latronico, Maria Candida B V Fragoso
Progress in Molecular Biology and Translational Science|April 9, 2010
Human diseases associated with GPR54 mutationsMilena Gurgel Teles, Leticia Ferreira Gontijo Silveira, Suzy Bianco, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 14, 2019
Pitfalls in the diagnosis of insulin autoimmune syndrome (Hirata's disease) in a hypoglycemic child: a case report and review of the literatureTiago Jeronimo Dos Santos, Caroline Gouvêa Buff Passone, Marina Ybarra, et al.
The Journal of Clinical Endocrinology and Metabolism|May 8, 2008
Factors determining normal adult height in girls with gonadotropin-dependent precocious puberty treated with depot gonadotropin-releasing hormone analogsVinicius Nahime Brito, Ana Claudia Latronico, Priscilla Cukier, et al.
Diabetes Research and Clinical Practice|April 26, 2022
Clinical and genetic characterization and long-term evaluation of individuals with maturity-onset diabetes of the young (MODY): The journey towards appropriate treatmentPedro Campos Franco, Lucas Santos de Santana, Aline Dantas Costa-Riquetto, et al.
Communications Medicine|October 24, 2025
Enhancing the diagnostic yield of monogenic diabetes in unresolved cases with early-onset hyperglycemiaPedro Campos Franco, Augusto Cezar Santomauro, Aline Dantas Costa-Riquetto, et al.
The New England Journal of Medicine|February 15, 2008
A GPR54-activating mutation in a patient with central precocious pubertyMilena Gurgel Teles, Suzy D C Bianco, Vinicius Nahime Brito, et al.
Hormone Research in Paediatrics|September 21, 2013
Molecular and gene network analysis of thyroid transcription factor 1 (TTF1) and enhanced at puberty (EAP1) genes in patients with GnRH-dependent pubertal disordersPriscilla Cukier, Hollis Wright, Tomke Rulfs, et al.
Clinical Endocrinology|June 4, 2009
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1Ericka Barbosa Trarbach, Milena Gurgel Teles, Elaine Maria Frade Costa, et al.
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