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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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Epidemiology, diagnosis and management of hirsutism: a consensus statement by the Androgen Excess and Polycystic Ovary Syndrome Society

Human reproduction update, 2012-03, Vol.18 (2), p.146-170

2012

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The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophy

Journal of neurology, neurosurgery and psychiatry, 2006-10, Vol.77 (10), p.1177-1179

2006

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Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism

The journal of clinical endocrinology and metabolism, 2000-11, Vol.85 (11), p.4013-4018

2000

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The frequency of CYP 21 gene mutations in Turkish women with hyperandrogenism

Experimental and clinical endocrinology & diabetes, 2009-05, Vol.117 (5), p.205-208

2009

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Mutational characterization of steroid 21-hydroxylase gene in Portuguese patients with congenital adrenal hyperplasia

Experimental and clinical endocrinology & diabetes, 2010-08, Vol.118 (8), p.505-512

2010

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The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations

Fertility and sterility, 1999-10, Vol.72 (4), p.629-638

1999

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Molecular genetics and pathophysiology of 17β-hydroxysteroid dehydrogenase 3 deficiency

The journal of clinical endocrinology and metabolism, 1996, Vol.81 (1), p.130-136

1996

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Early metabolic abnormalities in adolescent girls with polycystic ovarian syndrome

The Journal of pediatrics, 2001-01, Vol.138 (1), p.38-44

2001

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Evidence for a heterozygote advantage in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1997-07, Vol.82 (7), p.2097-2101

1997

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The role of heterozygosity for CYP21 in the polycystic ovary syndrome

Journal of pediatric endocrinology & metabolism : JPEM, 2000, Vol.13 Suppl 5, p.1315

2000

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Newborn screening for 21-hydroxylase deficiency: Results of CYP21 molecular genetic analysis

The Journal of pediatrics, 1997-08, Vol.131 (2), p.328-331

1997

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Neuropsychological Functioning in Girls with Premature Adrenarche

Journal of the International Neuropsychological Society, 2012-01, Vol.18 (1), p.151-156

2012

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Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1996-11, Vol.81 (11), p.4081-4088

1996

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Treatment of central precocious puberty : Comparison of urinary gonadotropin excretion and gonadotropin-releasing hormone (GnRH) stimulation tests in monitoring GnRH analog therapy

The journal of clinical endocrinology and metabolism, 1996-04, Vol.81 (4), p.1353-1356

1996

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21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study

American journal of obstetrics and gynecology, 2000-12, Vol.183 (6), p.1468-1474

2000

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De novo der(X)t(X;10)(q26;q21) with features of distal trisomy 10q: case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR)

Journal of medical genetics, 1997-03, Vol.34 (3), p.242-245

1997

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Ovarian responses to hCG stimulation: insulin resistance/hyperinsulinaemia vs. insulin deficiency

Clinical endocrinology (Oxford), 1999-07, Vol.51 (1), p.127-130

1999

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Absence of microdeletions in the Y chromosome in patients with a history of cryptorchidism and azoospermia or oligospermia

Fertility and sterility, 1999-04, Vol.71 (4), p.697-700

1999

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Disorders of sex development

Yearbook of Paediatric Endocrinology, 2018-09

SF, Witchel

2018

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Effects of different insulin sensitisers in the management of polycystic ovary syndrome: A systematic review and meta‐analysis

Clinical endocrinology (Oxford), 2024-02, Vol.100 (2), p.149-163

2024

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CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency

Human genetics, 2000-04, Vol.106 (4), p.414-419

2000

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Candidate gene analysis in premature pubarche and adolescent hyperandrogenism

Fertility and sterility, 2001-04, Vol.75 (4), p.724-730

2001

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Use of Gonadotropin-Releasing Hormone Analogs in Children: Update by an International Consortium

Hormone research in paediatrics, 2019, Vol.91 (6), p.357-372

2019

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No association between body mass index and beta(3)-adrenergic receptor variant (W64R) in children with premature pubarche and adolescent girls with hyperandrogenism

Fertility and sterility, 2000-03, Vol.73 (3), p.509-515

2000

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

Epidemiology, diagnosis and management of hirsutism: a consensus statement by the Androgen Excess and Polycystic Ovary Syndrome Society

The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophy

Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism

The frequency of CYP 21 gene mutations in Turkish women with hyperandrogenism

Mutational characterization of steroid 21-hydroxylase gene in Portuguese patients with congenital adrenal hyperplasia

The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations

Molecular genetics and pathophysiology of 17β-hydroxysteroid dehydrogenase 3 deficiency

Early metabolic abnormalities in adolescent girls with polycystic ovarian syndrome

Evidence for a heterozygote advantage in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The role of heterozygosity for CYP21 in the polycystic ovary syndrome

Newborn screening for 21-hydroxylase deficiency: Results of CYP21 molecular genetic analysis

Neuropsychological Functioning in Girls with Premature Adrenarche

Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Treatment of central precocious puberty : Comparison of urinary gonadotropin excretion and gonadotropin-releasing hormone (GnRH) stimulation tests in monitoring GnRH analog therapy

21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study

De novo der(X)t(X;10)(q26;q21) with features of distal trisomy 10q: case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR)

Ovarian responses to hCG stimulation: insulin resistance/hyperinsulinaemia vs. insulin deficiency

Absence of microdeletions in the Y chromosome in patients with a history of cryptorchidism and azoospermia or oligospermia

Disorders of sex development

Effects of different insulin sensitisers in the management of polycystic ovary syndrome: A systematic review and meta‐analysis

CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency

Candidate gene analysis in premature pubarche and adolescent hyperandrogenism

Use of Gonadotropin-Releasing Hormone Analogs in Children: Update by an International Consortium

No association between body mass index and beta(3)-adrenergic receptor variant (W64R) in children with premature pubarche and adolescent girls with hyperandrogenism

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