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Subnormal androgen and elevated progesterone levels in women treated for congenital virilizing 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1993-04, Vol.76 (4), p.933-936

1993

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Failure of Cortisone Acetate Treatment in Congenital Adrenal Hyperplasia because of Defective 11β-Hydroxysteroid Dehydrogenase Reductase Activity

The journal of clinical endocrinology and metabolism, 1999-04, Vol.84 (4), p.1210-1213

1999

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Prophylactic adrenalectomy of a three-year-old girl with congenital adrenal hyperplasia : Pre- and postoperative studies

The journal of clinical endocrinology and metabolism, 1997-10, Vol.82 (10), p.3324-3327

1997

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Characterisation of novel missense mutations in the GH receptor gene causing severe growth retardation

European journal of endocrinology, 2000-07, Vol.143 (1), p.71-76

2000

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Improved final height in girls with Turner's syndrome treated with growth hormone and oxandrolone

The journal of clinical endocrinology and metabolism, 1996-02, Vol.81 (2), p.635-640

1996

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An Androgen Receptor Gene Mutation (E653K) in a Family with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency as well as in Partial Androgen Insensitivity

The journal of clinical endocrinology and metabolism, 2002-06, Vol.87 (6), p.2623-2628

2002

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The use of adrenalectomy as a treatment for congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1996-09, Vol.81 (9), p.3180-3190

1996

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Improved final height in girls with Turner's syndrome treated with growth hormone and oxandrolone

The journal of clinical endocrinology and metabolism, 1996-02, Vol.81 (2), p.635-640

1996

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Adrenals of patients with severe forms of congenital adrenal hyperplasia do more harm than good

The journal of clinical endocrinology and metabolism, 1996-09, Vol.81 (9), p.3182

1996

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An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity : The impact of the human genome on endocrinology: Special features

The journal of clinical endocrinology and metabolism, 2002, Vol.87 (6), p.2623-2628

2002

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Demonstration of Estrogen Receptor-β Immunoreactivity in Human Growth Plate Cartilage

The journal of clinical endocrinology and metabolism, 1999-01, Vol.84 (1), p.370-373

1999

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21-Hydroxylase deficiency: disease-causing mutations categorized by densitometry of 21-hydroxylase-specific deoxyribonucleic acid fragments

The journal of clinical endocrinology and metabolism, 1990, Vol.70 (1), p.43-48

1990

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Defective 11β-HSD reductase activity in a patient with congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 2001, Vol.86 (3), p.1426

2001

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Discontinuation of growth hormone (GH) treatment: Metabolic effects in GH-deficient and GH-sufficient adolescent patients compared with control subjects

The journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4516-4524

1999

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Failure of cortisone acetate treatment in congenital adrenal hyperplasia because of defective 11beta-hydroxysteroid dehydrogenase reductase activity

The journal of clinical endocrinology and metabolism, 1999-04, Vol.84 (4), p.1210-1213

1999

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Somatomedin A levels in serum from healthy children and from children with growth hormone deficiency or delayed puberty

Acta endocrinologica (Copenhagen), 1980-06, Vol.94 (2), p.155-165

1980

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The use of adrenalectomy as a treatment for congenital adrenal hyperplasia. Controversy

The journal of clinical endocrinology and metabolism, 1996, Vol.81 (9), p.3180-3190

1996

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Prophylactic Adrenalectomy of a Three-Year-Old Girl with Congenital Adrenal Hyperplasia: Pre- and Postoperative Studies

The journal of clinical endocrinology and metabolism, 1997-10, Vol.82 (10), p.3324-3327

1997

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Defective 11β-HSD Reductase Activity in a Patient with Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2001-03, Vol.86 (3), p.1426-1427

2001

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Somatomedin A in human serum, determined by radioreceptor assay

Acta endocrinologica (Copenhagen), 1976-06, Vol.82 (3), p.449-459

1976

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In vitro simulation of stage-specific deoxyribonucleic acid synthesis in rat seminiferous tubule segments by interleukin-1α

Endocrinology (Philadelphia), 1991, Vol.129 (3), p.1614-1620

1991

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The use of adrenalectomy as a treatment for congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1996-09, Vol.81 (9), p.3180-3190

1996

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Identification of the main gonadal autoantigens in patients with adrenal insufficiency and associated ovarian failure

The journal of clinical endocrinology and metabolism, 1995-05, Vol.80 (5), p.1717-1723

1995

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Somatomedin A and B in serum from neonates, their mothers and cord blood

Acta endocrinologica (Copenhagen), 1977-07, Vol.85 (3), p.636-643

1977

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Incomplete androgen insensitivity: asymmetry in morphology and steroid profile and metabolism of the gonads. An analysis of a case

Acta endocrinologica (Copenhagen), 1985-12, Vol.110 (4), p.564-571

1985

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Subnormal androgen and elevated progesterone levels in women treated for congenital virilizing 21-hydroxylase deficiency

Failure of Cortisone Acetate Treatment in Congenital Adrenal Hyperplasia because of Defective 11β-Hydroxysteroid Dehydrogenase Reductase Activity

Prophylactic adrenalectomy of a three-year-old girl with congenital adrenal hyperplasia : Pre- and postoperative studies

Characterisation of novel missense mutations in the GH receptor gene causing severe growth retardation

Improved final height in girls with Turner's syndrome treated with growth hormone and oxandrolone

An Androgen Receptor Gene Mutation (E653K) in a Family with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency as well as in Partial Androgen Insensitivity

The use of adrenalectomy as a treatment for congenital adrenal hyperplasia

Improved final height in girls with Turner's syndrome treated with growth hormone and oxandrolone

Adrenals of patients with severe forms of congenital adrenal hyperplasia do more harm than good

An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity : The impact of the human genome on endocrinology: Special features

Demonstration of Estrogen Receptor-β Immunoreactivity in Human Growth Plate Cartilage

21-Hydroxylase deficiency: disease-causing mutations categorized by densitometry of 21-hydroxylase-specific deoxyribonucleic acid fragments

Defective 11β-HSD reductase activity in a patient with congenital adrenal hyperplasia

Discontinuation of growth hormone (GH) treatment: Metabolic effects in GH-deficient and GH-sufficient adolescent patients compared with control subjects

Failure of cortisone acetate treatment in congenital adrenal hyperplasia because of defective 11beta-hydroxysteroid dehydrogenase reductase activity

Somatomedin A levels in serum from healthy children and from children with growth hormone deficiency or delayed puberty

The use of adrenalectomy as a treatment for congenital adrenal hyperplasia. Controversy

Prophylactic Adrenalectomy of a Three-Year-Old Girl with Congenital Adrenal Hyperplasia: Pre- and Postoperative Studies

Defective 11β-HSD Reductase Activity in a Patient with Congenital Adrenal Hyperplasia

Somatomedin A in human serum, determined by radioreceptor assay

In vitro simulation of stage-specific deoxyribonucleic acid synthesis in rat seminiferous tubule segments by interleukin-1α

The use of adrenalectomy as a treatment for congenital adrenal hyperplasia

Identification of the main gonadal autoantigens in patients with adrenal insufficiency and associated ovarian failure

Somatomedin A and B in serum from neonates, their mothers and cord blood

Incomplete androgen insensitivity: asymmetry in morphology and steroid profile and metabolism of the gonads. An analysis of a case

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