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Satisfaction with Genital Surgery and Sexual Life of Adults with XY Disorders of Sex Development: Results from the German Clinical Evaluation Study

The journal of clinical endocrinology and metabolism, 2012-02, Vol.97 (2), p.577-588

2012

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Undescended testes: a consensus on management

European journal of endocrinology, 2008-12, Vol.159 Suppl 1 (suppl_1), p.S87-S90

Ritzén, E Martin

2008

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Cognitive Functions in Children at Risk for Congenital Adrenal Hyperplasia Treated Prenatally with Dexamethasone

The journal of clinical endocrinology and metabolism, 2007-02, Vol.92 (2), p.542-548

2007

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Prenatal Dexamethasone Treatment of Children at Risk for Congenital Adrenal Hyperplasia: The Swedish Experience and Standpoint

The journal of clinical endocrinology and metabolism, 2012-06, Vol.97 (6), p.1881-1883

2012

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The Role of Bilateral Adrenalectomy in the Treatment of Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2003-07, Vol.88 (7), p.2993-2998

2003

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Boys with Undescended Testes: Endocrine, Volumetric and Morphometric Studies on Testicular Function before and after Orchidopexy at Nine Months or Three Years of Age

The journal of clinical endocrinology and metabolism, 2012-12, Vol.97 (12), p.4588-4595

2012

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Endocrine Dysfunction in Prader-Willi Syndrome: A Review with Special Reference to GH

Endocrine reviews, 2001-12, Vol.22 (6), p.787-799

2001

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Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.3872-3880

1998

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Mutational spectrum of the steroid 21-hydroxylase gene in Sweden : implications for genetic diagnosis and association with disease manifestation

The journal of clinical endocrinology and metabolism, 1994-05, Vol.78 (5), p.1145-1152

1994

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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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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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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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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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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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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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Satisfaction with Genital Surgery and Sexual Life of Adults with XY Disorders of Sex Development: Results from the German Clinical Evaluation Study

Undescended testes: a consensus on management

Cognitive Functions in Children at Risk for Congenital Adrenal Hyperplasia Treated Prenatally with Dexamethasone

Prenatal Dexamethasone Treatment of Children at Risk for Congenital Adrenal Hyperplasia: The Swedish Experience and Standpoint

The Role of Bilateral Adrenalectomy in the Treatment of Congenital Adrenal Hyperplasia

Boys with Undescended Testes: Endocrine, Volumetric and Morphometric Studies on Testicular Function before and after Orchidopexy at Nine Months or Three Years of Age

Endocrine Dysfunction in Prader-Willi Syndrome: A Review with Special Reference to GH

Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasia

Mutational spectrum of the steroid 21-hydroxylase gene in Sweden : implications for genetic diagnosis and association with disease manifestation

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

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

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

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

Somatomedin A in human serum, determined by radioreceptor assay

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

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