Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency

by Larissa G. Gomes, Guiomar Madureira, Berenice B. Mendonca, Tania A. S. S. Bachega
Published 2013-01-01

An update of genetic basis of PCOS pathogenesis

by Raiane P. Crespo, Tania A. S. S. Bachega, Berenice B. Mendonça, Larissa G. Gomes

Impact of glucocorticoid receptor gene polymorphisms on the metabolic profile of adult patients with the classical form of 21-hydroxylase deficiency.

by Ricardo P P Moreira, Larissa G Gomes, Berenice B Mendonca, Tânia A S S Bachega
Published 2012-01-01

Frequency of genetic polymorphisms of PXR gene in the Brazilian population

by Ricardo P. P. Moreira, Alexander A. L. Jorge, Berenice B. Mendonca, Tânia A. S. S. Bachega
Published 2011-01-01

Influence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia

by Ricardo P. P. Moreira, Larissa G. Gomes, Guiomar Madureira, Berenice B. Mendonca, Tânia A. S. S. Bachega
Published 2014-01-01

Applicability of a novel mathematical model for the prediction of adult height and age at menarche in girls with idiopathic central precocious puberty

by Mateus Cavarzan Lopes, Carolina Oliveira Ramos, Ana Claudia Latronico, Berenice B. Mendonça, Vinicius N. Brito
Published 2018-07-01

Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure

by Braian Lucas A. Sousa, Mirian Yumie Nishi, Mariza Gerdulo Santos, Vinicius Nahime Brito, Sorahia Domenice, Berenice B. Mendonca

Primary malignant tumors of the adrenal glands

by Madson Q. Almeida, Joao Evangelista Bezerra-Neto, Berenice B. Mendonça, Ana Claudia Latronico, Maria Candida B.V. Fragoso
Published 2018-12-01

An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles

by Viviani De-Marco, Luciani R. Carvalho, Mariana F. Guzzo, Paulo S.L. Oliveira, Larissa G. Gomes, Berenice B. Mendonca

Population and mutation analysis of Y-STR loci in a sample from the city of São Paulo (Brazil)

by José A. Soares-Vieira, Ana E.C. Billerbeck, Edna S.M. Iwamura, Berenice B. Mendonca, Leonor Gusmão, Paulo A. Otto
Published 2008-01-01

Modulatory effect of BclI GR gene polymorphisms on the obesity phenotype in Brazilian patients with Cushing's disease

by Ricardo P.P. Moreira, Tânia A.S.S. Bachega, Márcio C. Machado, Berenice B. Mendonca, Marcello D. Bronstein, Maria Candida B. Villares Fragoso
Published 2013-05-01

PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without β-catenin mutations

by Carolina M.G Cani, Hamilton Matushita, Luciani R. S Carvalho, Ibere C Soares, Luciana P Brito, Madson Q Almeida, Berenice B Mendonça
Published 2011-01-01

Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

by Ricardo P. P. Moreira, Alexander A. L. Jorge, Larissa G. Gomes, Laura C. Kaupert, João Massud Filho, Berenice B. Mendonca, Tânia A. S. S. Bachega
Published 2011-01-01

Long-term follow-up of a female with congenital adrenal hyperplasia due to P450-oxidoreductase deficiency

by Beatriz D. S. F. Bonamichi, Stella L. M. Santiago, Débora R. Bertola, Chong A. Kim, Nivaldo Alonso, Berenice B. Mendonca, Tania A. S. S. Bachega, Larissa G. Gomes
Published 2016-10-01

ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome

by Renata C Scalco, Ericka B Trarbach, Edoarda V A Albuquerque, Thais K Homma, Thais H Inoue-Lima, Mirian Y Nishi, Berenice B Mendonca, Alexander A L Jorge
Published 2019-12-01

PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation

by Ricardo V. Araujo, Claudia V. Chang, Valter A. S. Cescato, Maria Candida B. V. Fragoso, Marcello D. Bronstein, Berenice B. Mendonca, Ivo J. P. Arnhold, Luciani R. S. Carvalho
Published 2013-06-01

Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery

by Fernanda A. Correa, Marilena Nakaguma, João L. O. Madeira, Mirian Y. Nishi, Milena G. Abrão, Alexander A. L. Jorge, Luciani R. Carvalho, Ivo J. P. Arnhold, Berenice B. Mendonça
Published 2019-05-01

Association of glucocorticoid receptor polymorphisms with clinical and metabolic profiles in polycystic ovary syndrome

by Gustavo A.Rosa Maciel, Ricardo P.P. Moreira, Diogo D.G. Bugano, Sylvia A.Y. Hayashida, José A.M. Marcondes, Larissa G. Gomes, Berenice B. Mendonça, Tânia A.S.S. Bachega, Edmund C. Baracat
Published 2014-03-01

Isolated familial somatotropinoma: 11Q13-LOH and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis

by Rodrigo A. Toledo, Berenice B. Mendonca, Maria Candida B. V. Fragoso, Iberê C. Soares, Madson Q. Almeida, Michelle B. Moraes, Delmar M. Lourenço-Jr, Venâncio A. F. Alves, Marcello D. Bronstein, Sergio P. A. Toledo
Published 2010-01-01

Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency.

by Monica M França, Mariana F A Funari, Antonio M Lerario, Mariza G Santos, Mirian Y Nishi, Sorahia Domenice, Daniela R Moraes, Everlayny F Costalonga, Gustavo A R Maciel, Andrea T Maciel-Guerra, Gil Guerra-Junior, Berenice B Mendonca
Published 2020-01-01