Works matching AU Mendonca, Berenice B.

Results: 152

SLC25A11, a Novel Gene Associated With Carney-Stratakis Syndrome.

Published in:

Journal of the Endocrine Society, 2025, v. 9, n. 5, p. 1, doi. 10.1210/jendso/bvaf052

By:

Freitas-Castro, Felipe;
Santana, Lucas S;
Fagundes, Gustavo F C;
Lobato, Eduardo C;
Afonso, Ana Caroline F;
Nakamura, Izabel T;
Ledesma, Felipe L;
Soares, Ibere C;
Mendonca, Berenice B;
Latronico, Ana Claudia;
Stratakis, Constantine A;
Almeida, Madson Q

Publication type:

Article

Identification of Predictors of Metastatic Potential in Paragangliomas to Develop a Prognostic Score (PSPGL).

Published in:

Journal of the Endocrine Society, 2024, v. 8, n. 7, p. 1, doi. 10.1210/jendso/bvae093

By:

Iguchi, Daniela Yone Veiga;
Filho, Sebastião Nunes Martins;
Soares, Iberê Cauduro;
Siqueira, Sheila Aparecida Coelho;
Alves, Venâncio Avancini Ferreira;
Assato, Aline Kawassaki;
Yang, Ji Hoon;
Almeida, Madson Q;
Fragoso, Maria Candida Barisson Villares;
Fagundes, Gustavo Freitas Cardoso;
Mendonca, Berenice B;
Junior, Delmar Muniz Lourenço;
Hoff, Ana O;
Castroneves, Luciana Audi;
Ferraz-de-Souza, Bruno;
Giannella, Maria Lucia Cardillo Correa;
Pereira, Maria Adelaide Albergaria

Publication type:

Article

Clinical and Pathological Predictors of Death for Adrenocortical Carcinoma.

Published in:

Journal of the Endocrine Society, 2024, v. 8, n. 4, p. 1, doi. 10.1210/jendso/bvad170

By:

Pato, Eduardo;
Srougi, Victor;
Zerbini, Claudia;
Ledesma, Felipe L;
Tanno, Fabio;
Almeida, Madson Q;
Nahas, William;
Latronico, Ana Claudia;
Mendonca, Berenice B;
Chambô, Jose L;
Fragoso, Maria Candida B V

Publication type:

Article

Efficacy of Oral Furosemide Test for Primary Aldosteronism Diagnosis.

Published in:

Journal of the Endocrine Society, 2024, v. 8, n. 1, p. 1, doi. 10.1210/jendso/bvad147

By:

Freitas, Thais C;
Maciel, Ana Alice W;
Fagundes, Gustavo F C;
Petenuci, Janaina;
Santana, Lucas S;
Guimaraes, Augusto G;
Freitas-Castro, Felipe;
Srougi, Victor;
Tanno, Fabio Y;
Chambo, Jose L;
Pereira, Maria Adelaide A;
Brito, Luciana P;
Pio-Abreu, Andrea;
Bortolotto, Luiz A;
Latronico, Ana Claudia;
Fragoso, Maria Candida B V;
Drager, Luciano F;
Mendonca, Berenice B;
Almeida, Madson Q

Publication type:

Article

High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort.

Published in:

Journal of the Endocrine Society, 2022, v. 6, n. 9, p. 1, doi. 10.1210/jendso/bvac106

By:

Crespo, Raiane P;
Rocha, Thais P;
Montenegro, Luciana R;
Nishi, Mirian Y;
Jorge, Alexander A L;
Maciel, Gustavo A R;
Baracat, Edmund;
Latronico, Ana Claudia;
Mendonca, Berenice B;
Gomes, Larissa G

Publication type:

Article

Comprehensive Genetic Analysis of 128 Candidate Genes in a Cohort With Idiopathic, Severe, or Familial Osteoporosis.

Published in:

Journal of the Endocrine Society, 2020, v. 4, n. 12, p. 1, doi. 10.1210/jendso/bvaa148

By:

Rocha-Braz, Manuela G M;
França, Monica M;
Fernandes, Adriana M;
Lerario, Antonio M;
Zanardo, Evelin A;
Santana, Lucas S de;
Kulikowski, Leslie D;
Martin, Regina M;
Mendonca, Berenice B;
Ferraz-de-Souza, Bruno

Publication type:

Article

A New Insight into the Surgical Treatment of Primary Macronodular Adrenal Hyperplasia.

Published in:

Journal of the Endocrine Society, 2020, v. 4, n. 8, p. 1, doi. 10.1210/jendso/bvaa083

By:

Tanno, Fabio Yoshiaki;
Srougi, Victor;
Almeida, Madson Q;
Yamauchi, Fernando Ide;
Coelho, Fernando Morbeck Almeida;
Nishi, Mirian Yumie;
Zerbini, Maria Claudia Nogueira;
Soares, Iracy Silvia Correa;
Pereira, Maria Adelaide Albergaria;
Charchar, Helaine Laiz Silva;
Lacombe, Amanda Meneses Ferreira;
Brondani, Vania Balderrama;
Srougi, Miguel;
Nahas, Willian Carlos;
Mendonca, Berenice B;
Chambô, José Luis;
Fragoso, Maria Candida Barisson Villares

Publication type:

Article

New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations.

Published in:

Journal of the Endocrine Society, 2019, v. 3, n. 9, p. 1682, doi. 10.1210/js.2019-00225

By:

Fagundes, Gustavo F C;
Petenuci, Janaina;
Lourenco, Delmar M;
Trarbach, Ericka B;
Pereira, Maria Adelaide A;
D'Eur, Joya Emilie Correa;
Hoff, Ana O;
Lerario, Antonio M;
Zerbini, Maria Claudia N;
Siqueira, Sheila;
Yamauchi, Fernando;
Srougi, Victor;
Tanno, Fabio Y;
Chambo, Jose Luis;
Latronico, Ana Claudia;
Mendonca, Berenice B;
Fragoso, Maria Candida B V;
Almeida, Madson Q

Publication type:

Article

Impact of Long-Term Dexamethasone Therapy on the Metabolic Profile of Patients With 21-Hydroxylase Deficiency.

Published in:

Journal of the Endocrine Society, 2019, v. 3, n. 8, p. 1574, doi. 10.1210/js.2019-00123

By:

Seraphim, Carlos E;
Frassei, Juliana S;
Pessoa, Bruna S;
Scalco, Renata C;
Miranda, Mirela C;
Madureira, Guiomar;
Mendonca, Berenice B;
Bachega, Tania A S S

Publication type:

Article

Persistent Poor Metabolic Profile in Postmenopausal Women With Ovarian Hyperandrogenism After Testosterone Level Normalization.

Published in:

Journal of the Endocrine Society, 2019, v. 3, n. 5, p. 1087, doi. 10.1210/js.2018-00405

By:

Rocha, Thaís;
Crespo, Raiane P;
Yance, Viviane V R;
Hayashida, Sylvia A;
Baracat, Edmund C;
Carvalho, Filomena;
Domenice, Sorahia;
Mendonca, Berenice B;
Gomes, Larissa G

Publication type:

Article

Anorexia as the first clinical manifestation of von Hippel-Lindau syndrome.

Published in:

Molecular & Clinical Oncology, 2020, v. 13, n. 5, p. N.PAG, doi. 10.3892/mco.2020.2135

By:

Marques, Julia Hatagami;
Batista, Rafael Loch;
Moraes, Mariana Teichner De;
Morais, Barbara Albuquerque;
Pinto, Fernando Campos Gomes;
Almeida, Madson Q.;
Aragão, Denise De Cássia;
Teixeira, Manoel Jacobsen;
Mendonca, Berenice B.;
Cordás, Táki Athanássios

Publication type:

Article

Novel Mutations in CYP11B1 Gene Leading to 11β-Hydroxylase Deficiency in Brazilian Patients.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 9, p. 3481, doi. 10.1210/jc.2008-2521

By:

Soardi, Fernanda C.;
Penachioni, Junia Y.;
Justo, Giselle Z.;
Bachega, Tânia A. S. S.;
Inácio, Marlene;
Mendonça, Berenice B.;
de Castro, Margaret;
de Mello, Maricilda P.

Publication type:

Article

Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency.

Published in:

2009

By:

Gomes, Larissa G;
Huang, Ningwu;
Agrawal, Vishal;
Mendonça, Berenice B;
Bachega, Tania A S S;
Miller, Walter L

Publication type:

journal article

Expression of Insulin-Like Growth Factor-II and Its Receptor in Pediatric and Adult Adrenocortical Tumors.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 9, p. 3524, doi. 10.1210/jc.2008-0065

By:

Almeida, Madson Q.;
Barisson Villares Fragoso, Maria Candida;
Pacicco Lotfi, Claudimara Ferini;
Santos, Mariza Gerdulo;
Nishi, Mirian Yumie;
Soares Costa, Marcia Helena;
Lerario, Antonio Marcondes;
Maciel, Carolina Canton;
Mattos, Gabriele Ebling;
Lima Jorge, Alexander Augusto;
Mendonca, Berenice B.;
Latronico, Ana Claudia

Publication type:

Article

The common P450 oxidoreductase variant A503V is not a modifier gene for 21-hydroxylase deficiency.

Published in:

2008

By:

Gomes, Larissa G;
Huang, Ningwu;
Agrawal, Vishal;
Mendonça, Berenice B;
Bachega, Tania A S S;
Miller, Walter L

Publication type:

journal article

Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 12, p. 4889, doi. 10.1210/jc.2007-1661

By:

Coutinho, Debora C.;
Coletta, Rocio R. D.;
Costa, Elaine M. F.;
Pachi, Paulo R.;
Boguszewski, Margaret C. S.;
Damiani, Durval;
Mendonca, Berenice B.;
Arnhold, Ivo J. P.;
Jorge, Alexander A. L.

Publication type:

Article

Microconversion between CYP21A2 and CYP21A1P promoter regions causes the nonclassical form of 21-hydroxylase deficiency.

Published in:

2007

By:

Araújo, Rogério S;
Mendonca, Berenice B;
Barbosa, Angela S;
Lin, Chin J;
Marcondes, José A M;
Billerbeck, Ana Elisa C;
Bachega, Tânia A S S

Publication type:

journal article

Growth Hormone (GH) Pharmacogenetics: Influence of GH Receptor Exon 3 Retention or Deletion on First-Year Growth Response and Final Height in Patients with Severe GH Deficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 3, p. 1076, doi. 10.1210/jc.2005-2005

By:

Jorge, Alexander A. L.;
Marchisotti, Frederico G.;
Montenegro, Luciana R.;
Carvalho, Luciani R.;
Mendonca, Berenice B.;
Arnhold, Ivo J. P.

Publication type:

Article

Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 5, p. 2976, doi. 10.1210/jc.2004-0963

By:

Pinto, Emilia M.;
C. Billerbeck, Ana Elisa;
Villares Fragoso, Maria Candida B.;
Mendonca, Berenice B.;
Latronico, Ana Claudia

Publication type:

Article

Refining Hormonal Diagnosis of Type II 3β- Hydroxysteroid Dehydrogenase Deficiency in Patients with Premature Pubarche and Hirsutism Based on HSD3B2 Genotyping.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 3, p. 1287, doi. 10.1210/jc.2004-1552

By:

Mermejo, Livia M.;
Elias, Lucila L. K.;
Marui, S.;
Moreira, Ayrton C.;
Mendonca, Berenice B.;
Margaret de Castro

Publication type:

Article

A Single Luteinizing Hormone Determination 2 Hours after Depot Leuprolide Is Useful for Therapy Monitoring of Gonadotropin-Dependent Precocious Puberty in Girls.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 9, p. 4338, doi. 10.1210/jc.2003-031537

By:

BRITO, VINICIUS N.;
LATRONICO, ANA C.;
ARNHOLD, IVO J. P.;
MENDONCA, BERENICE B.

Publication type:

Article

A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 4, p. 1767, doi. 10.1210/jc.2003-031240

By:

CORREA, RAFAELA V.;
DOMENICE, SORAHIA;
BINGHAM, NATHAN C.;
BILLERBECK, ANA ELISA C.;
RAINEY, WILLIAM E.;
PARKER, KEITH L.;
MENDONCA, BERENICE B.

Publication type:

Article

P450c17 deficiency in Brazilian patients: biochemical diagnosis through progesterone levels confirmed by CYP17 genotyping.

Published in:

2003

By:

Martin, Regina M.;
Lin, Chin J.;
Costa, Elaine M. F.;
de Oliveira, Maria Leocadia;
Carrilho, Alexandre;
Villar, Heloisa;
Longui, Carlos A.;
Mendonca, Berenice B.

Publication type:

journal article

Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3027, doi. 10.1210/jc.2002-021780

By:

MARTIN, REGINA M.;
LIN, CHIN J.;
NISHI, MIRIAN Y.;
BILLERBECK, ANA ELISA C.;
LATRONICO, ANA CLAUDIA;
RUSSELL, DAVID W.;
MENDONCA, BERENICE B.

Publication type:

Article

Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3241, doi. 10.1210/jc.2002-021658

By:

MELO, KARLA F. S.;
MENDONCA, BERENICE B.;
BILLERBECK, ANA ELISA C.;
COSTA, ELAINE M. F.;
INÁCIO, MARLENE;
SILVA, FREDERICO A. Q.;
LEAL, ANGELA M. O.;
LATRONICO, ANA C.;
ARNHOLD, IVO J. P.

Publication type:

Article

Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3027, doi. 10.1210/jc.2002-021780

By:

MARTIN, REGINA M.;
LIN, CHIN J.;
NISHI, MIRIAN Y.;
BILLERBECK, ANA ELISA C.;
LATRONICO, ANA CLAUDIA;
RUSSELL, DAVID W.;
MENDONCA, BERENICE B.

Publication type:

Article

Pituitary Magnetic Resonance Imaging and Function in Patients with Growth Hormone Deficiency with and without Mutations in GHRH-R, GH-1, or PROP-1 Genes.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 11, p. 5076, doi. 10.1210/jc.2001-011936

By:

OSORIO, MARIA GERALDA F.;
MARUI, SUEMI;
JORGE, ALEXANDER A. L.;
LATRONICO, ANA C.;
LO, LEONARD S. S.;
LEITE, CLAUDIA C.;
ESTEFAN, VIVIAN;
MENDONCA, BERENICE B.;
ARNHOLD, IVO J. P.

Publication type:

Article

Three novel mutations in CYP21 gene in Brazilian patients with the classical form of 21-hydroxylase deficiency due to a founder effect.

Published in:

2002

By:

Billerbeck, Ana Elisa C;
Mendonca, Berenice B;
Pinto, Emilia M;
Madureira, Guiomar;
Arnhold, Ivo J P;
Bachega, Tânia A S S

Publication type:

journal article

An Unusual Phenotype of Frasier Syndrome due to IVS9 +4C>T Mutation in the WT1 Gene: Predominantly Male Ambiguous Genitalia and Absence of Gonadal Dysgenesis.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 6, p. 2500, doi. 10.1210/jcem.87.6.8521

By:

MELO, KARLA F. S.;
MARTIN, REGINA M.;
COSTA, ELAINE M. F.;
CARVALHO, FILOMENA M.;
JORGE, ALEXANDER A.;
ARNHOLD, IVO J. P.;
MENDONCA, BERENICE B.

Publication type:

Article

Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 4, p. 1805, doi. 10.1210/jcem.87.4.8379

By:

MENDONCA, BERENICE B.;
LEITE, MARISTELA V.;
DE CASTRO, MARGARET;
KINO, TOMOSHIGE;
ELIAS, LUCILA L. K.;
BACHEGA, TANIA A. S.;
ARNHOLD, IVO J. P.;
CHROUSOS, GEORGE P.;
LATRONICO, ANA CLAUDIA

Publication type:

Article

Poor Reproducibility of IGF-I and IGF Binding Protein-3 Generation Test in Children with Short Stature and Normal Coding Region of the GH Receptor Gene.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 2, p. 469, doi. 10.1210/jcem.87.2.8191

By:

JORGE, ALEXANDER A.;
SOUZA, SILVIA C.;
ARNHOLD, IVO J.;
MENDONCA, BERENICE B.

Publication type:

Article

Variable ACTH-stimulated 17-hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations.

Published in:

2002

By:

BACHEGA, TÂNIA A.S. S.;
BRENLHA, ENECY M. L.;
BILLERBECK, ANA E. C.;
MARCONDES, JOSÉ A. M.;
MADUREIRA, GUIOMAR;
Arnhold, Ivo J.P.;
Mendonca, Berenice B.

Publication type:

journal article

Absence of Mutations Involving the Lim Homeobox Domain Gene LHX9 in 46,XY Gonadal Agenesis and Dysgenesis.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 6, p. 2465, doi. 10.1210/jcem.86.6.7539

By:

OTTOLENGHI, CHRIS;
MOREIRA-FILHO, CARLOS;
MENDONÇA, BERENICE B.;
BARBIERI, MARCELLO;
FELLOUS, MARC;
BERKOVITZ, GARY D.;
MCELREAVEY, KEN

Publication type:

Article

Gonadotropin-Independent Precocious Puberty Due to Luteinizing Hormone Receptor Mutations in Brazilian Boys: A Novel Constitutively Activating Mutation in the First Transmembrane Helix.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 12, p. 4799, doi. 10.1210/jcem.85.12.7071

By:

LATRONICO, ANA CLAUDIA;
SHINOZAKI, HIROMITSU;
GUERRA JR., GIL;
PEREIRA, MARIA ADELAIDE A.;
LEMOS MARINI, SOFIA HELENA V.;
BAPTISTA, MARIA TEREZA M.;
ARNHOLD, IVO JORGE P.;
FANELLI, FRANCESCA;
MENDONCA, BERENICE B.;
SEGALOFF, DEBORAH L.

Publication type:

Article

Origin of an Ovarian Steroid Cell Tumor Causing Isosexual Pseudoprecocious Puberty Demonstrated by the Expression of Adrenal Steroidogenic Enzymes and Adrenocorticotropin Receptor.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 3, p. 1211, doi. 10.1210/jcem.85.3.6454

By:

LIN, CHIN J.;
JORGE, ALEXANDER A. L.;
LATRONICO, ANA CLAUDIA;
MARUI, SUEMI;
FRAGOSO, MARIA CANDIDA V.;
MARTIN, REGINA M.;
CARVALHO, FILOMENA M.;
ARNHOLD, IVO J. P.;
MENDONCA, BERENICE B.

Publication type:

Article

17β-Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 12, p. 4713, doi. 10.1210/jc.84.12.4713

By:

BOEHMER, ANNEMIE L. M.;
BRINKMANN, ALBERT O.;
SANDKUIJL, LODEWIJK A.;
HALLEY, DICKY J. J.;
NIERMEIJER, MARTINUS F.;
ANDERSSON, STEFAN;
DE JONG, FRANK H.;
KAYSERILI, HÜLYA;
DE VROEDE, MONIQUE A.;
OTTEN, BARTO J.;
ROUWÉ, CATRIENUS W.;
MENDONÇA, BERENICE B.;
RODRIGUES, CIDADE;
BODE, HANS H.;
DE RUITER, PETRA E.;
DELEMARRE-VAN DE WAAL, HENRIETTE A.;
DROP, STENVERT L. S.

Publication type:

Article

A Novel Missense Mutation, GLY424SER, in Brazilian Patients with 21-Hydroxylase Deficiency.

Published in:

1999

By:

BILLERBECK, ANA ELISA C.;
BACHEGA, TÂNIA A. S. S.;
FRAZZATTO, ELIANA T.;
MIRIAN YUMIE NISHI;
GOLDBERG, ANNA CARLA;
MARIN, MARIA LUCIA C.;
MADUREIRA, GUIOMAR;
MONTE, OSMAR;
ARNHOLD, IVO J. P.;
MENDONCA, BERENICE B.

Publication type:

journal article

Longitudinal Hormonal and Pituitary Imaging Changes in Two Females with Combined Pituitary Hormone Deficiency due to Deletion of A301,G302 in the PROP1 Gene.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 3, p. 942, doi. 10.1210/jcem.84.3.5537

By:

MENDONCA, BERENICE B.;
OSORIO, MARIA G. F.;
LATRONICO, ANA CLAUDIA;
ESTEFAN, VIVIAN;
SU SIH LO, LEONARD;
ARNHOLD, IVO J. P.

Publication type:

Article

17b-Hydroxysteroid Dehydrogenase 3 Deficiency in Women.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 2, p. 802, doi. 10.1210/jcem.84.2.5477

By:

MENDONCA, BERENICE B.;
ARNHOLD, IVO J. P.;
BLOISE, WALTER;
ANDERSSON, STEFFAN;
RUSSELL, DAVID W.;
WILSON, JEAN D.

Publication type:

Article

Molecular Genotyping in Brazilian Patients with the Classical and Nonclassical Forms of 21-Hydroxylase Deficiency*.

Published in:

1998

By:

BACHEGA, TÂNIA A. S. S.;
BILLERBECK, ANA ELISA C.;
MADUREIRA, GUIOMAR;
MARCONDES, JOSÉ A. M.;
LONGUI, CARLOS A.;
LEITE, MARISTELA V.;
ARNHOLD, IVO J. P.;
MENDONCA, BERENICE B.

Publication type:

journal article

The PROP1 2-Base Pair Deletion Is a Common Cause of Combined Pituitary Hormone Deficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 9, p. 3346, doi. 10.1210/jc.83.9.3346

By:

COGAN, JOY D.;
WEI WU;
PHILLIPS III, JOHN A.;
ARNHOLD, IVO J. P.;
AGAPITO, ANA;
FOFANOVA, OLGA V.;
OSORIO, MARIA GERALDA F.;
BIRCAN, IFFET;
MORENO, ADOLFO;
MENDONCA, BERENICE B.

Publication type:

Article

Activating Mutation of the Stimulatory G Protein (gsp) as a Putative Cause of Ovarian and Testicular Human Stromal Leydig Cell Tumors

Published in:

Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 6, p. 2074, doi. 10.1210/jcem.83.6.4847

By:

VILLARES FRAGOSO, MARIA CANDIDA B.;
LATRONICO, ANA CLAUDIA;
CARVALHO, FILOMENA MARINO;
ZERBINI, MARIA CLAUDIA N.;
MIGUEL MARCONDES, JOSE ANTONIO;
ARAUJO, LEILA M. B.;
LANDO, VALERIA S.;
FRAZZATTO, ELIANA T.;
MENDONCA, BERENICE B.;
VILLARES, SANDRA MARA F.

Publication type:

Article

Molecular Genetics and Pathophysiology of 17β-Hydroxysteroid Dehydrogenase 3 Deficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1996, v. 81, n. 1, p. 130, doi. 10.1210/jc.81.1.130

By:

ANDERSSON, STEFAN;
GEISSLER, WAYNE M.;
LING WU;
DAVIS, DAPHNE L.;
GRUMBACH, MELVIN M.;
NEW, MARIA I.;
SCHWARZ, HANS P.;
BLETHEN, SANDRA L.;
MENDONCA, BERENICE B.;
BLOISE, WALTER;
WITCHEL, SELMA F.;
CUTLER, JR., GORDON B.;
GRIFFIN, JAMES E.;
WILSON, JEAN D.;
RUSSELL, DAVID W.

Publication type:

Article

Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency.

Published in:

2014

By:

Santos, Mariza G;
Machado, Aline Z;
Martins, Conceiçao N;
Domenice, Sorahia;
Costa, Elaine M F;
Nishi, Mirian Y;
Ferraz-de-Souza, Bruno;
Jorge, Soraia A C;
Pereira, Carlos A;
Soardi, Fernanda C;
de Mello, Maricilda P;
Maciel-Guerra, Andrea T;
Guerra-Junior, Gil;
Mendonca, Berenice B;
Martins, Conceição N

Publication type:

journal article

Severe and Mild Neonatal Hypothyroidism Mediate Opposite Effects on Leydig Cells of Rats.

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Thyroid, 2002, v. 12, n. 1, p. 13, doi. 10.1089/105072502753451913

By:

Cristovão, Fatima C.;
Bisi, Helio;
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Bloise, Walter

Publication type:

Article

Effects of long-term storage of filter paper blood samples on neonatal thyroid stimulating hormone, thyroxin and 17-alpha-hydroxyprogesterone measurements.

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Journal of Medical Screening, 2008, v. 15, n. 3, p. 109, doi. 10.1258/jms.2008.007086

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Lando, Valeria S.;
Batista, Marcelo C.;
Nakamura, Izabel T.;
Mazi, Cassia R.;
Mendonca, Berenice B.;
Brito, Vinicius N.

Publication type:

Article

Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency.

Published in:

PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0044893

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Moreira, Ricardo P. P.;
Gomes, Larissa G.;
Mendonca, Berenice B.;
Bachega, Tânia A. S. S.;
Laudet, Vincent

Publication type:

Article

Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells.

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Pediatric & Developmental Pathology, 2010, v. 13, n. 5, p. 375, doi. 10.2350/08-12-0578.1

By:

Lovisolo, Silvana M.;
Mendonça, Berenice B.;
Pinto, Emilia M.;
Manna, Thais Della;
Saldiva, Paulo Hilário N.;
Zerbini, Maria Cláudia N.

Publication type:

Article

CONGENITAL HYPERINSULINISM IN BRAZILIAN NEONATES: A STUDY OF HISTOLOGY, KATP CHANNEL GENES AND PROLIFERATION OF β-CELLS.

Published in:

Pediatric & Developmental Pathology, 2010, v. 13, n. 3, p. 1

By:

Lovisolo, Silvana M.;
Mendonça, Berenice B.;
Pinto, Emilia M.;
Manna, Thais Della;
Saldiva, Paulo Hilário N.;
Zerbini, Maria Cláudia N.

Publication type:

Article

Genetic and clinical aspects of paediatric pheochromocytomas and paragangliomas.

Published in:

Clinical Endocrinology, 2021, v. 95, n. 1, p. 117, doi. 10.1111/cen.14467

By:

Petenuci, Janaina;
Guimaraes, Augusto G.;
Fagundes, Gustavo F.C.;
Benedetti, Anna Flavia F.;
Afonso, Ana Caroline F.;
Pereira, Maria Adelaide A.;
Zerbini, Maria Claudia N.;
Siqueira, Sheila;
Yamauchi, Fernando;
Soares, Silvia C.;
Srougi, Victor;
Tanno, Fabio Y.;
Chambo, Jose L.;
Lopes, Roberto I.;
Denes, Francisco T.;
Hoff, Ana O.;
Latronico, Ana Claudia;
Mendonca, Berenice B.;
Fragoso, Maria Candida B. V.;
Almeida, Madson Q.

Publication type:

Article