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Nordic consensus on treatment of undescended testes

Acta Paediatrica, 2007-05, Vol.96 (5), p.638-643

2007

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Growth hormone treatment improves vitality and behavioural issues in children with Prader-Willi syndrome

Acta Paediatrica, 2015-01, Vol.104 (1), p.59-67

2015

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Growth of spontaneously descended and surgically treated testes during early childhood

Pediatrics (Evanston), 2013-04, Vol.131 (4), p.e1174-e1180

2013

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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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Surgical Treatment of Unilaterally Undescended Testes: Testicular Growth After Randomization to Orchiopexy at Age 9 Months or 3 Years

The Journal of urology, 2007-10, Vol.178 (4), p.1589-1593

2007

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Dose-Dependent Effect of Growth Hormone on Final Height in Children with Short Stature without Growth Hormone Deficiency

The journal of clinical endocrinology and metabolism, 2008, Vol.93 (11), p.4342-4350

2008

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Cryptorchidism: a clinical perspective

Pediatric endocrinology reviews : PER, 2014-02, Vol.11 Suppl 2, p.240

2014

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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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Treating fetal thyroid and adrenal disorders through the mother

Nature clinical practice. Endocrinology & metabolism, 2008-12, Vol.4 (12), p.675-682

2008

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Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 Cotreatment versus Insulin-Like Growth Factor-I Alone in Two Brothers with Growth Hormone Insensitivity Syndrome: Effects on Insulin Sensitivity, Body Composition and Linear Growth

Hormone research in paediatrics, 2011-01, Vol.76 (5), p.355-366

2011

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Long-term follow-up of prenatally treated children at risk for congenital adrenal hyperplasia: does dexamethasone cause behavioural problems?

European journal of endocrinology, 2008-09, Vol.159 (3), p.309-316

2008

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Testicular growth from birth to two years of age, and the effect of orchidopexy at age nine months : A randomized, controlled study

Acta pædiatrica (Oslo), 2006-03, Vol.95 (3), p.318-324

2006

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Localization of estrogen receptors-alpha and -beta and androgen receptor in the human growth plate at different pubertal stages

Journal of endocrinology, 2003-05, Vol.177 (2), p.319-326

2003

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Development and descent of the testis in relation to cryptorchidism

Acta Paediatrica, 2007-05, Vol.96 (5), p.622-627

2007

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Steroid 21-Hydroxylase Deficiency: Three Additional Mutated Alleles and Establishment of Phenotype-Genotype Relationships of Common Mutations

Proceedings of the National Academy of Sciences - PNAS, 1992-08, Vol.89 (15), p.7232-7236

1992

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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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Management of undescended testes: how and when?

Pediatric endocrinology reviews : PER, 2009-09, Vol.7 (1), p.32

2009

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Early puberty: what is normal and when is treatment indicated?

Hormone research, 2003-01, Vol.60 Suppl 3 (Suppl. 3), p.31-34

Ritzen, EM

2003

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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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Very Long-Term Follow-Up of Girls with Early and Late Menarche

Abnormalities in Puberty, 2005, Vol.8, p.126-136

2005

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Does Growth Hormone Treatment Influence Pubertal Development in Short Children?

Hormone research in paediatrics, 2011-01, Vol.76 (4), p.262-272

2011

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Bone mass and body composition of adult women with congenital virilizing 21-hydroxylase deficiency after glucocorticoid treatment since infancy

European journal of endocrinology, 2000-11, Vol.143 (5), p.667-671

2000

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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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Management of males with 45,X/46,XY gonadal dysgenesis

Hormone research, 1999, Vol.52 (1), p.11-14

1999

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Nordic consensus on treatment of undescended testes

Growth hormone treatment improves vitality and behavioural issues in children with Prader-Willi syndrome

Growth of spontaneously descended and surgically treated testes during early childhood

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

Surgical Treatment of Unilaterally Undescended Testes: Testicular Growth After Randomization to Orchiopexy at Age 9 Months or 3 Years

Dose-Dependent Effect of Growth Hormone on Final Height in Children with Short Stature without Growth Hormone Deficiency

Cryptorchidism: a clinical perspective

Undescended testes: a consensus on management

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

Treating fetal thyroid and adrenal disorders through the mother

Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 Cotreatment versus Insulin-Like Growth Factor-I Alone in Two Brothers with Growth Hormone Insensitivity Syndrome: Effects on Insulin Sensitivity, Body Composition and Linear Growth

Long-term follow-up of prenatally treated children at risk for congenital adrenal hyperplasia: does dexamethasone cause behavioural problems?

Testicular growth from birth to two years of age, and the effect of orchidopexy at age nine months : A randomized, controlled study

Localization of estrogen receptors-alpha and -beta and androgen receptor in the human growth plate at different pubertal stages

Development and descent of the testis in relation to cryptorchidism

Steroid 21-Hydroxylase Deficiency: Three Additional Mutated Alleles and Establishment of Phenotype-Genotype Relationships of Common Mutations

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

Management of undescended testes: how and when?

Early puberty: what is normal and when is treatment indicated?

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

Very Long-Term Follow-Up of Girls with Early and Late Menarche

Does Growth Hormone Treatment Influence Pubertal Development in Short Children?

Bone mass and body composition of adult women with congenital virilizing 21-hydroxylase deficiency after glucocorticoid treatment since infancy

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

Management of males with 45,X/46,XY gonadal dysgenesis

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