G. Madureira

发表

Anatomical and functional outcomes of feminizing genitoplasty for ambiguous genitalia in patients with virilizing congenital adrenal hyperplasia.

F. Dénes, M. H. Sircili, B. B. de Mendonça, 2006, Clinics.

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

B. Mendonca, L. Gomes, T. S. Bachega, 2014, International journal of endocrinology.

The Cost-Effectiveness of Congenital Adrenal Hyperplasia Newborn Screening in Brazil: A Comparison Between Screened and Unscreened Cohorts

D. Damiani, A. Cassenote, E. Trindade, 2021, Frontiers in Pediatrics.

Clinical, hormonal and pathological findings in a comparative study of adrenocortical neoplasms in childhood and adulthood.

A. Halpern, A. Latronico, B. Mendonca, 1995, The Journal of urology.

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

L. Haddad, B. B. de Mendonça, G. Madureira, 2019, Journal of the Endocrine Society.

Premature Pubarche due to Exogenous Testosterone Gel or Intense Diaper Rash Prevention Cream Use: A Case Series

A. Latronico, D. Macedo, C. Ramos, 2019, Hormone Research in Paediatrics.

The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene

F. S. Cunha, J. Marcondes, B. B. de Mendonça, 2016, PloS one.

21-Hydroxylase deficiency in Brazil.

C. Longui, I. Arnhold, B. Mendonca, 2000, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

C. Longui, B. Mendonca, I. Arnhold, 1999, Human Heredity.

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

B. Mendonca, L. Gomes, G. Madureira, 2013, Clinics.

Male pseudohermaphroditism due to 5 alpha reductase deficiency associated with gynecomastia.

W. Bloise, B. Mendonca, M. C. Batista, 1987, Revista do Hospital das Clinicas.

Prepubertal male pseudohermaphroditism due to 17-ketosteroid reductase deficiency: diagnostic value of a hCG test and lack of HLA association

I. Arnhold, W. Bloise, B. Mendonca, 1988, Journal of endocrinological investigation.

Quality of life of patients with 46,XX and 46,XY disorders of sex development

B. Mendonca, I. Arnhold, L. Gomes, 2015, Clinical endocrinology.

Adrenal Nodules in Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Regression after Adequate Hormonal Control

B. Mendonca, I. Arnhold, G. Madureira, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Endocrine interaction between zinc and prolactin

J. Brandão-Neto, B. Mendonca, W. Bloise, 1995, Biological Trace Element Research.

Quality of life in a large cohort of adult Brazilian patients with 46,XX and 46,XY disorders of sex development from a single tertiary centre

B. Mendonca, I. Arnhold, F. Dénes, 2014, Clinical endocrinology.

Neonatal 17‐hydroxyprogesterone levels adjusted according to age at sample collection and birthweight improve the efficacy of congenital adrenal hyperplasia newborn screening

B. Mendonca, V. Brito, G. Madureira, 2017, Clinical endocrinology.

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

B. Mendonca, R. Scalco, G. Madureira, 2019, Journal of the Endocrine Society.

Molecular CYP21A2 diagnosis in 480 Brazilian patients with congenital adrenal hyperplasia before newborn screening introduction.

H. Kuperman, D. Damiani, B. Mendonca, 2016, European journal of endocrinology.

A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency.

O. Monte, I. Arnhold, M. Nishi, 1999, The Journal of clinical endocrinology and metabolism.

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

E. Pinto, B. Mendonca, I. Arnhold, 2002, The Journal of clinical endocrinology and metabolism.

Substitutions in the CYP21A2 promoter explain the simple‐virilizing form of 21‐hydroxylase deficiency in patients harbouring a P30L mutation

B. Mendonca, A. Billerbeck, G. Madureira, 2005, Clinical endocrinology.

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

B. Mendonca, I. Arnhold, A. Billerbeck, 2002, The Journal of clinical endocrinology and metabolism.

Influence of different genotypes on 17‐hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21‐hydroxylase deficiency

B. Mendonca, I. Arnhold, A. Billerbeck, 2000, Clinical endocrinology.

Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency.

C. Longui, I. Arnhold, B. Mendonca, 1998, The Journal of clinical endocrinology and metabolism.

X 21-Hydroxylase deficiency in Brazil

C. Longui, I. Arnhold, B. Mendonca, 2022 .

Endocrine interaction between zinc and prolactin. An interpretative review.

J. Brandão-Neto, B. Mendonca, W. Bloise, 1995, Biological trace element research.

Surgical Treatment after Failed Primary Correction of Urogenital Sinus in Female Patients with Virilizing Congenital Adrenal Hyperplasia: Are Good Results Possible?

B. Mendonca, F. Dénes, L. Gomes, 2016, Frontiers in Pediatrics.

Leydig cell hypoplasia causing male pseudohermaphroditism: case report and review of the literature.

W. Bloise, S. Toledo, H. Bisi, 1987, Revista do Hospital das Clínicas.

Effect of Acute and Chronic Oral Zinc Administration in Hyperprolactinemic Patients

J. Brandão-Neto, B. Mendonca, W. Bloise, 1999, Metal-Based Drugs.

Molecular CYP21A2 diagnosis in 480 Brazilian patients with congenital adrenal hyperplasia before newborn screening introduction.

H. Kuperman, D. Damiani, B. Mendonca, 2016, European journal of endocrinology.

Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia

B. Mendonca, S. Villares, G. Madureira, 2013, Hormone Research in Paediatrics.

Influence of the A 3669 G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia

B. Mendonca, L. Gomes, G. Madureira, 2014 .