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Reproductive Outcome of Women with 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2006-09, Vol.91 (9), p.3451-3456

2006

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CYP21A2 genotypes do not predict the severity of hyperandrogenic manifestations in the nonclassical form of congenital adrenal hyperplasia

Hormone and metabolic research, 2013-04, Vol.45 (4), p.301-307

2013

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Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia

Clinical genetics, 2009-12, Vol.76 (6), p.503-510

2009

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Zona fasciculata 21-hydroxysteroids and precursor-to-product ratios in 21-hydroxylase deficiency: Further characterization of classic and non-classic patients and heterozygote carriers

Journal of endocrinological investigation, 2011-09, Vol.34 (8), p.587-592

2011

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

The journal of clinical endocrinology and metabolism, 1998-12, Vol.83 (12), p.4416-4419

1998

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Reproductive Outcome of Women With 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia

Obstetrical & gynecological survey, 2007-02, Vol.62 (2), p.106-108

2007

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

Clinical endocrinology (Oxford), 2000-05, Vol.52 (5), p.601-607

2000

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

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2870-2872

1999

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Adrenal steroids synthesis during acute infectious diseases in infants

Journal of Pediatric Endocrinology and Metabolism, 2002-11, Vol.15 (9), p.1515

2002

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

Human heredity, 1999-01, Vol.49 (1), p.9-14

1999

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Growth Potential in Congenital Adrenal Hyperplasia(Cah) Due To 21-Hydroxylase Deficiency Treated With Cortisone Acetate(Ca) and Fludrohidrocortisone(Fh)

Pediatric research, 1997-02, Vol.41 (2), p.302-302

1997

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Frequency of Deletions and Gene Conversions in Brazilian Patients With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency

Pediatric research, 1997-02, Vol.41 (2), p.302-302

1997

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3 ADRENAL IMAGE STUDIES IN PATIENTS WITH CONGENITAL ADRENAL HYPERLASIA DUE TO 21-HYDROXYLASE DEFICIENCY

Pediatric research, 1994-11, Vol.36 (5), p.678-678

1994

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Characterization of 8 Point Mutations in the Cyp21b Gene in Brazilian Patients With Congenital Adrenal Hyperplasia (Cah) Due To 21-Hydroxylase Deficiency 31

Pediatric research, 1998-02, Vol.43 (2), p.300-300

1998

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Plasma Renin Measurements are Unrelated to Mineralocorticoid Replacement Dose in Patients With Primary Adrenal Insufficiency

The journal of clinical endocrinology and metabolism, 2020-01, Vol.105 (1), p.314-326

2020

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Disorders of sex development: effect of molecular diagnostics

Nature reviews. Endocrinology, 2015-08, Vol.11 (8), p.478-488

2015

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Acoustic Injectors for Drop-On-Demand Serial Femtosecond Crystallography

Structure (London), 2016-04, Vol.24 (4), p.631-640

2016

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A genome-wide association study identified loci for yield component traits in sugarcane (Saccharum spp.)

PloS one, 2019-07, Vol.14 (7), p.e0219843-e0219843

2019

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Elucidating Enzymatic Catalysis Using Fast Quantum Chemical Descriptors

Journal of chemical information and modeling, 2020-02, Vol.60 (2), p.578-591

2020

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An update of genetic basis of PCOS pathogenesis

Archives of endocrinology and metabolism, 2018-06, Vol.62 (3), p.352-361

2018

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Classic congenital adrenal hyperplasia and its impact on reproduction

Fertility and sterility, 2019-01, Vol.111 (1), p.7-12

2019

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Long-term cardio-metabolic outcomes in patients with classical congenital adrenal hyperplasia: is the risk real?

Current opinion in endocrinology, diabetes, and obesity, 2020-06, Vol.27 (3), p.155-161

2020

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

Clinical endocrinology (Oxford), 2017-04, Vol.86 (4), p.480-487

2017

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Low Adrenomedullary Function Predicts Acute Illness in Infants With Classical Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2022-01, Vol.107 (1), p.e264-e271

2022

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Reproductive Outcome of Women with 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia

CYP21A2 genotypes do not predict the severity of hyperandrogenic manifestations in the nonclassical form of congenital adrenal hyperplasia

Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia

Zona fasciculata 21-hydroxysteroids and precursor-to-product ratios in 21-hydroxylase deficiency: Further characterization of classic and non-classic patients and heterozygote carriers

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

Reproductive Outcome of Women With 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia

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

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

Adrenal steroids synthesis during acute infectious diseases in infants

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

Growth Potential in Congenital Adrenal Hyperplasia(Cah) Due To 21-Hydroxylase Deficiency Treated With Cortisone Acetate(Ca) and Fludrohidrocortisone(Fh)

Frequency of Deletions and Gene Conversions in Brazilian Patients With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency

3 ADRENAL IMAGE STUDIES IN PATIENTS WITH CONGENITAL ADRENAL HYPERLASIA DUE TO 21-HYDROXYLASE DEFICIENCY

Characterization of 8 Point Mutations in the Cyp21b Gene in Brazilian Patients With Congenital Adrenal Hyperplasia (Cah) Due To 21-Hydroxylase Deficiency 31

Plasma Renin Measurements are Unrelated to Mineralocorticoid Replacement Dose in Patients With Primary Adrenal Insufficiency

Disorders of sex development: effect of molecular diagnostics

Acoustic Injectors for Drop-On-Demand Serial Femtosecond Crystallography

A genome-wide association study identified loci for yield component traits in sugarcane (Saccharum spp.)

Elucidating Enzymatic Catalysis Using Fast Quantum Chemical Descriptors

An update of genetic basis of PCOS pathogenesis

Classic congenital adrenal hyperplasia and its impact on reproduction

Long-term cardio-metabolic outcomes in patients with classical congenital adrenal hyperplasia: is the risk real?

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

Low Adrenomedullary Function Predicts Acute Illness in Infants With Classical Congenital Adrenal Hyperplasia

Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry

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