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COMMENTARY: A Window of Opportunity: The Diagnosis of Gonadotropin Deficiency in the Male Infant

The journal of clinical endocrinology and metabolism, 2005-05, Vol.90 (5), p.3122-3127

Grumbach, Melvin M

2005

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The neuroendocrinology of human puberty revisited

Hormone research, 2002-01, Vol.57 Suppl 2 (Suppl. 2), p.2-14

Grumbach, Melvin M

2002

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Management of the clinically inapparent adrenal mass ("incidentaloma")

Annals of internal medicine, 2003-03, Vol.138 (5), p.424

2003

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Increased Bone Mass as a Result of Estrogen Therapy in a Man with Aromatase Deficiency

The New England journal of medicine, 1998-08, Vol.339 (9), p.599-603

1998

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Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens

The journal of clinical endocrinology and metabolism, 1995-12, Vol.80 (12), p.3689-3698

1995

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Estrogen, bone, growth and sex: a sea change in conventional wisdom

Journal of pediatric endocrinology & metabolism : JPEM, 2000-12, Vol.13 Suppl 6, p.1439

Grumbach, M M

2000

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Congenital hypogonadotropic hypogonadism and micropenis: Effect of testosterone treatment on adult penile size—Why sex reversal is not indicated

The Journal of pediatrics, 1999-05, Vol.134 (5), p.579-583

1999

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Mutations in the Synthesis and Action of Estrogen: The Critical Role in the Male of Estrogen on Pubertal Growth, Skeletal Maturation, and Bone Mass

Annals of the New York Academy of Sciences, 2004-12, Vol.1038 (1), p.7-13

GRUMBACH, MELVIN M.

2004

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Consensus Statement on 21-Hydroxylase Deficiency from The Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology

The journal of clinical endocrinology and metabolism, 2002-09, Vol.87 (9), p.4048-4053

2002

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A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom)

The journal of clinical endocrinology and metabolism, 1994-06, Vol.78 (6), p.1287-1292

1994

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PREGNANCY OUTCOMES IN WOMEN WITH CONGENITAL VIRILIZING ADRENAL HYPERPLASIA

Endocrinology and metabolism clinics of North America, 2001-03, Vol.30 (1), p.207-229

2001

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Idiopathic hypothalamic diabetes insipidus, pituitary stalk thickening, and the occult intracranial germinoma in children and adolescents

The journal of clinical endocrinology and metabolism, 1997-05, Vol.82 (5), p.1362-1367

1997

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Molecular Basis of Aromatase Deficiency in an Adult Female with Sexual Infantilism and Polycystic Ovaries

Proceedings of the National Academy of Sciences - PNAS, 1993-12, Vol.90 (24), p.11673-11677

1993

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Long-term outcome in children and adolescents after transsphenoidal surgery for Cushing's disease

The journal of clinical endocrinology and metabolism, 1997-10, Vol.82 (10), p.3196-3202

1997

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Normal female infants born of mothers with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.930-936

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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Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society

Hormone research, 2002-01, Vol.58 (4), p.188-195

2002

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Long term effect of gonadotropin-releasing hormone agonist therapy on final and near-final height in 26 children with true precocious puberty treated at a median age of less than 5 years

The journal of clinical endocrinology and metabolism, 1995-02, Vol.80 (2), p.546-551

1995

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N-methyl-D-aspartate (NMDA) receptors mediate the release of gonadotropin-releasing hormone (GnRH) by NMDA in a hypothalamic GnRH neuronal cell line (GT1-1)

Endocrinology (Philadelphia), 1994-03, Vol.134 (3), p.1023-1030

1994

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The luteinizing hormone-releasing hormone-secreting hypothalamic hamartoma is a congenital malformation natural history

The journal of clinical endocrinology and metabolism, 1993-07, Vol.77 (1), p.118-124

1993

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The growth hormone cascade: progress and long-term results of growth hormone treatment in growth hormone deficiency

Hormone research, 1998-01, Vol.49 Suppl 2 (Suppl. 2), p.41-57

1998

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Nitric oxide synthesized by gonadotropin-releasing hormone neurons is a mediator of N-methyl-D-aspartate (NMDA)-induced GnRH secretion

Endocrinology (Philadelphia), 1994-10, Vol.135 (4), p.1709-1712

1994

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The role of estrogen in the male and female: evidence from mutations in synthesis and action

Hormone research, 2000-01, Vol.53 Suppl 3 (3), p.23-24

Grumbach, M M

2000

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Clinical review 14 : pathophysiology and treatment of sexual precocity

The journal of clinical endocrinology and metabolism, 1990-10, Vol.71 (4), p.785-789

1990

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MR imaging of Kallmann syndrome, a genetic disorder of neuronal migration affecting the olfactory and genital systems

American journal of neuroradiology, 1993-07, Vol.14 (4), p.827-838

1993

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COMMENTARY: A Window of Opportunity: The Diagnosis of Gonadotropin Deficiency in the Male Infant

The neuroendocrinology of human puberty revisited

Management of the clinically inapparent adrenal mass ("incidentaloma")

Increased Bone Mass as a Result of Estrogen Therapy in a Man with Aromatase Deficiency

Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens

Estrogen, bone, growth and sex: a sea change in conventional wisdom

Congenital hypogonadotropic hypogonadism and micropenis: Effect of testosterone treatment on adult penile size—Why sex reversal is not indicated

Mutations in the Synthesis and Action of Estrogen: The Critical Role in the Male of Estrogen on Pubertal Growth, Skeletal Maturation, and Bone Mass

Consensus Statement on 21-Hydroxylase Deficiency from The Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology

A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom)

PREGNANCY OUTCOMES IN WOMEN WITH CONGENITAL VIRILIZING ADRENAL HYPERPLASIA

Idiopathic hypothalamic diabetes insipidus, pituitary stalk thickening, and the occult intracranial germinoma in children and adolescents

Molecular Basis of Aromatase Deficiency in an Adult Female with Sexual Infantilism and Polycystic Ovaries

Long-term outcome in children and adolescents after transsphenoidal surgery for Cushing's disease

Normal female infants born of mothers with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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

Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society

Long term effect of gonadotropin-releasing hormone agonist therapy on final and near-final height in 26 children with true precocious puberty treated at a median age of less than 5 years

N-methyl-D-aspartate (NMDA) receptors mediate the release of gonadotropin-releasing hormone (GnRH) by NMDA in a hypothalamic GnRH neuronal cell line (GT1-1)

The luteinizing hormone-releasing hormone-secreting hypothalamic hamartoma is a congenital malformation natural history

The growth hormone cascade: progress and long-term results of growth hormone treatment in growth hormone deficiency

Nitric oxide synthesized by gonadotropin-releasing hormone neurons is a mediator of N-methyl-D-aspartate (NMDA)-induced GnRH secretion

The role of estrogen in the male and female: evidence from mutations in synthesis and action

Clinical review 14 : pathophysiology and treatment of sexual precocity

MR imaging of Kallmann syndrome, a genetic disorder of neuronal migration affecting the olfactory and genital systems

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