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Compound heterozygous mutations of the luteinizing hormone receptor gene in Leydig cell hypoplasia

Molecular endocrinology (Baltimore, Md.), 1996-08, Vol.10 (8), p.987-997

1996

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COMPOUND HETEROZYGOUS MUTATIONS OF THE LUTEINIZING HORMONE/CHORIONIC GONADOTROPIN RECEPTOR GENE IN A FAMILY WITH TWO CHILDREN AFFECTED BY LEYDIG CELL HYPOPLASIA (LCH). • 387

Pediatric research, 1997-04, Vol.41, p.67-67

1997

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The ISMRM Open Science Initiative for Perfusion Imaging (OSIPI): Results from the OSIPI-Dynamic Contrast-Enhanced challenge

Magnetic resonance in medicine, 2024-05, Vol.91 (5), p.1803-1821

2024

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A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty

Nature (London), 1993-10, Vol.365 (6447), p.652-654

1993

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Genetic Heterogeneity of Constitutively Activating Mutations of the Human Luteinizing Hormone Receptor in Familial Male-Limited Precocious Puberty

Proceedings of the National Academy of Sciences - PNAS, 1995-03, Vol.92 (6), p.1906-1910

1995

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Mutations in the Ca(2+)-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism

Human molecular genetics, 1996-05, Vol.5 (5), p.601-606

1996

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Evidence for impaired activation of the hypothalamic-pituitary-adrenal axis in patients with chronic fatigue syndrome

The journal of clinical endocrinology and metabolism, 1991-12, Vol.73 (6), p.1224-1234

1991

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Mutations in the Ca2+-Sensing Receptor Gene Cause Autosomal Dominant and Sporadic Hypoparathyroidism

Human molecular genetics, 1996-05, Vol.5 (5), p.601-606

1996

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A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia

Human molecular genetics, 1995-08, Vol.4 (8), p.1429-1433

1995

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Testicular adrenal rest tissue in congenital adrenal hyperplasia: findings at Gray-scale and color Doppler US

Radiology, 1996-01, Vol.198 (1), p.99-104

1996

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A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1996-10, Vol.81 (10), p.3535-3539

1996

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Ligand-independent hormone secretion

Current opinion in pediatrics, 1995-08, Vol.7 (4), p.434-439

Laue, L

1995

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Sex Differences in Sensitivity of the Hypothalamic-Pituitary-Adrenal Axis

Health psychology, 1993-09, Vol.12 (5), p.420-425

1993

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Growth and neuroendocrine dysfunction in children with acquired immunodeficiency syndrome

The Journal of pediatrics, 1990-10, Vol.117 (4), p.541-545

1990

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Treatment of familial male precocious puberty with spironolactone, testolactone, and deslorelin

The journal of clinical endocrinology and metabolism, 1993, Vol.76 (1), p.151-155

1993

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Thyroid abnormalities in children infected with human immunodeficiency virus

The Journal of pediatrics, 1996, Vol.128 (1), p.70-74

1996

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Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

The New England journal of medicine, 1990-12, Vol.323 (26), p.1806-1813

1990

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Effect of chronic treatment with the glucocorticoid antagonist RU 486 in man : toxicity, immunological, and hormonal aspects

The journal of clinical endocrinology and metabolism, 1990-12, Vol.71 (6), p.1474-1480

1990

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Treatment of familial male precocious puberty with spironolactone and testolactone

The New England journal of medicine, 1989-02, Vol.320 (8), p.496-502

1989

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The antiglucocorticoid and antiprogestin steroid RU 486 suppresses the adrenocorticotropin response to ovine corticotropin releasing hormone in man

The journal of clinical endocrinology and metabolism, 1988-02, Vol.66 (2), p.290-293

1988

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Receptor-mediated effects of glucocorticoids on inflammation: Enhancement of the inflammatory response with a glucocorticoid antagonist

Journal of steroid biochemistry, 1988-06, Vol.29 (6), p.591-598

1988

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Congenital adrenal hyperplasia : Molecular genetics and alternative approaches to treatment

Advances in pediatrics, 1995, Vol.42 (1), p.113-143

1995

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The effect of mevinolin on steroidogenesis in patients with defects in the low density lipoprotein receptor pathway

The journal of clinical endocrinology and metabolism, 1987-03, Vol.64 (3), p.531-535

1987

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Adrenal androgen secretion in postadolescent acne : increased adrenocortical function without hypersensitivity to adrenocorticotropin

The journal of clinical endocrinology and metabolism, 1991-08, Vol.73 (2), p.380-384

1991

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Seminars in medicine of the beth Israel hospital, Boston : congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The New England journal of medicine, 1990-12, Vol.323 (26), p.1806-1813

1990

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Compound heterozygous mutations of the luteinizing hormone receptor gene in Leydig cell hypoplasia

COMPOUND HETEROZYGOUS MUTATIONS OF THE LUTEINIZING HORMONE/CHORIONIC GONADOTROPIN RECEPTOR GENE IN A FAMILY WITH TWO CHILDREN AFFECTED BY LEYDIG CELL HYPOPLASIA (LCH). • 387

The ISMRM Open Science Initiative for Perfusion Imaging (OSIPI): Results from the OSIPI-Dynamic Contrast-Enhanced challenge

A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty

Genetic Heterogeneity of Constitutively Activating Mutations of the Human Luteinizing Hormone Receptor in Familial Male-Limited Precocious Puberty

Mutations in the Ca(2+)-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism

Evidence for impaired activation of the hypothalamic-pituitary-adrenal axis in patients with chronic fatigue syndrome

Mutations in the Ca2+-Sensing Receptor Gene Cause Autosomal Dominant and Sporadic Hypoparathyroidism

A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia

Testicular adrenal rest tissue in congenital adrenal hyperplasia: findings at Gray-scale and color Doppler US

A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia

Ligand-independent hormone secretion

Sex Differences in Sensitivity of the Hypothalamic-Pituitary-Adrenal Axis

Growth and neuroendocrine dysfunction in children with acquired immunodeficiency syndrome

Treatment of familial male precocious puberty with spironolactone, testolactone, and deslorelin

Thyroid abnormalities in children infected with human immunodeficiency virus

Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Effect of chronic treatment with the glucocorticoid antagonist RU 486 in man : toxicity, immunological, and hormonal aspects

Treatment of familial male precocious puberty with spironolactone and testolactone

The antiglucocorticoid and antiprogestin steroid RU 486 suppresses the adrenocorticotropin response to ovine corticotropin releasing hormone in man

Receptor-mediated effects of glucocorticoids on inflammation: Enhancement of the inflammatory response with a glucocorticoid antagonist

Congenital adrenal hyperplasia : Molecular genetics and alternative approaches to treatment

The effect of mevinolin on steroidogenesis in patients with defects in the low density lipoprotein receptor pathway

Adrenal androgen secretion in postadolescent acne : increased adrenocortical function without hypersensitivity to adrenocorticotropin

Seminars in medicine of the beth Israel hospital, Boston : congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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