Mutation distributions among patients with congenital adrenal hyperplasia from five regions of Brazil: a systematic review

por Hosomi, Silvério S., Salles, Igor C., Bachega, Tânia A. S. S.
Publicado 2023

Adrenal crisis and mortality rate in adrenal insufficiency and congenital adrenal hyperplasia

por Lousada, Lia Mesquita, Mendonca, Berenice B., Bachega, Tania A. S. S.
Publicado 2021

Editorial: Molecular -genetic causes underlying primary adrenal insufficiency: Current insights into diagnosis and treatment

por Fragoso, Maria Candida B.V., Bachega, Tânia A. S. S., Dain, Liliana
Publicado 2022

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

por Gomes, Larissa G., Madureira, Guiomar, Mendonca, Berenice B., Bachega, Tania A. S. S.
Publicado 2013

An update of genetic basis of PCOS pathogenesis

por Crespo, Raiane P., Bachega, Tania A. S. S., Mendonça, Berenice B., Gomes, Larissa G.
Publicado 2018

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

por Moreira, Ricardo P. P., Gomes, Larissa G., Mendonca, Berenice B., Bachega, Tânia A. S. S.
Publicado 2012

Frequency of genetic polymorphisms of PXR gene in the Brazilian population

por Moreira, Ricardo P P, Jorge, Alexander A L, Mendonca, Berenice B, Bachega, Tânia A S S
Publicado 2011

PSAT072 Clinical Features of Patients with 21-Hydroxylase Deficiency and Testicular Adrenal Rest Tumors

por Bachega, Tânia A S S, Costa, Fernanda C, Madureira, Guiomar, Mendonca, Berenice B, Miranda, Mirela C
Publicado 2022

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

por Moreira, Ricardo P. P., Gomes, Larissa G., Madureira, Guiomar, Mendonca, Berenice B., Bachega, Tânia A. S. S.
Publicado 2014

Adverse Outcomes and Economic Burden of Congenital Adrenal Hyperplasia Late Diagnosis in the Newborn Screening Absence

por Miranda, Mirela Costa De, Haddad, Luciana Bertocco de Paiva, Madureira, Guiomar, de Mendonca, Berenice Bilharinho, Bachega, Tania A S S
Publicado 2019

Self-Reported Feelings of Adult Patients With Differences of Sex Development (DSD) Regarding Genital Surgical Procedures

por Lousada, Lia Mesquita, Domenice, Sorahia, Frade Costa, Elaine Maria, Bachega, Tania A, Batista, Rafael Loch, Mendonca, Berenice Bilharinho
Publicado 2021

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

por Moreira, Ricardo P. P., Bachega, Tânia A. S. S., Machado, Márcio C., Mendonca, Berenice B., Bronstein, Marcello D., Villares Fragoso, Maria Candida B.
Publicado 2013

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

por 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
Publicado 2019

Understanding, Communication and Concerns Around Sexual Development Differences by Patients’ Perspectives

por Lousada, Lia Mesquita, Domenice, Sorahia, Costa, Elaine Maria Frade, Bachega, Tania A, Batista, Rafael Loch, Fontenele, Eveline Gadelha Pereira, Mendonca, Berenice Bilharinho
Publicado 2021

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

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

SUN-071 Prenatal and Post-Natal Influence of Androgens in the Psychosexual Development in Individuals with 21-hydroxylase Congenital Adrenal Hyperplasia

por Batista, Rafael Loch, Inacio, Marlene, de Miranda, Mirela Costa, Gomes, Pedro Vasconcelos, Cabral, Hially R, Madureira, Guiomar, Mendonca, Berenice Bilharinho, Bachega, Tania A
Publicado 2020

Effects of Pre and Post-Natal Androgen Exposure on Psychosexual Aspects and Gender Change in Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

por Batista, Rafael Loch, Inacio, Marlene, de Miranda, Mirela Costa, Madureira, Guiomar, Gomes, Larissa Garcia, Rodrigues, Andresa De Santi, Bachega, Tania A, Mendonca, Berenice Bilharinho
Publicado 2021

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

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

SUN-172 A False Positive Result in Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in a Girl with Beckwith Wiedemann Syndrome

por Braga, Barbara Leitao, Feitosa, Klevia N, Maia, Thamiris Freitas, Madureira, Guiomar, Nishi, Mirian Yumie, Bachega, Tania A, Villares Fragoso, Maria Candida Barisson, Mendonca, Berenice Bilharinho
Publicado 2020

SUN-212 Interference in Serum Androstenedione Measured by LC-MS/MS in Newborns Samples

por Lima-Valassi, Helena Panteliou, Takitane, Juliana, Silva, Márcia Rodrigues, Alves, Atecla Nunciata Lopes, Hayashi, Giselle Yuri, Hadachi, Sonia Marchezi, Bachega, Tania A, Mendonca, Berenice Bilharinho
Publicado 2020