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Fertility and pregnancy outcome in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Human reproduction (Oxford), 2008-07, Vol.23 (7), p.1607-1613

2008

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Reply: The sex ratio of offspring of women with congenital adrenal hyperplasia

Human reproduction (Oxford), 2009-01, Vol.24 (1), p.251-251

2009

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A 31-year-old woman with infertility and polycystic ovaries diagnosed with non-classic congenital adrenal hyperplasia due to a novel CYP21 mutation

Journal of endocrinological investigation, 2008-02, Vol.31 (2), p.176-180

2008

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Molecular targets of a human HNF1α mutation responsible for pancreatic β-cell dysfunction

The EMBO journal, 2000-08, Vol.19 (16), p.4257-4264

2000

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The experience of women living with Congenital Adrenal Hyperplasia: impact of the condition and the care given

Clinical endocrinology (Oxford), 2016-07, Vol.85 (1), p.21-28

2016

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Gender Role Behavior, Sexuality, and Psychosocial Adaptation in Women with Congenital Adrenal Hyperplasia due to CYP21A2 Deficiency

The journal of clinical endocrinology and metabolism, 2009-09, Vol.94 (9), p.3432-3439

2009

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Identity, Sexuality, and Parenthood in Women with Congenital Adrenal Hyperplasia

Journal of pediatric & adolescent gynecology, 2020-10, Vol.33 (5), p.470-476

2020

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Ovarian epithelial neoplasia after hormonal infertility treatment: long-term follow-up of a historical cohort in Sweden

Fertility and sterility, 2009-04, Vol.91 (4), p.1152-1158

2009

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Sexual Function and Surgical Outcome in Women with Congenital Adrenal Hyperplasia Due to CYP21A2 Deficiency: Clinical Perspective and the Patients’ Perception

The journal of clinical endocrinology and metabolism, 2010-08, Vol.95 (8), p.3633-3640

2010

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Type of Mutation and Surgical Procedure Affect Long-Term Quality of Life for Women with Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2008-02, Vol.93 (2), p.380-386

2008

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Fractures and Bone Mineral Density in Adult Women with 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2007-12, Vol.92 (12), p.4643-4649

2007

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Metabolic Profile and Body Composition in Adult Women with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2007-01, Vol.92 (1), p.110-116

2007

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Voice problems due to virilization in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Clinical endocrinology (Oxford), 2013-12, Vol.79 (6), p.859-866

2013

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Prospective follow-up of menstrual disorders in adolescence and prognostic factors

Acta obstetricia et gynecologica Scandinavica, 2008-01, Vol.87 (11), p.1162-1168

2008

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Voice characteristics in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Clinical endocrinology (Oxford), 2009-01, Vol.70 (1), p.18-25

2009

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A nutrition study in juvenile elite gymnasts

Acta Paediatrica, 1995-03, Vol.84 (3), p.273-277

1995

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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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Bone mineral content of young female former gymnasts

Acta Paediatrica, 1995-10, Vol.84 (10), p.1109-1112

1995

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Increased Liver Enzymes in Adult Women with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Endocrine Journal, 2009, Vol.56(4), pp.601-608

2009

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Menstrual disorders and associated factors among adolescent girls visiting a youth clinic

Acta obstetricia et gynecologica Scandinavica, 2007, Vol.86 (1), p.65-72

2007

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Reduced bone mineral density in adult women diagnosed with menstrual disorders during adolescence

Acta obstetricia et gynecologica Scandinavica, 2009-01, Vol.88 (5), p.543-549

2009

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Cotreatment with growth hormone and gonadotropin for ovulation induction in hypogonadotropic patients: a prospective, randomized, placebo-controlled, dose-response study

Fertility and sterility, 1995-11, Vol.64 (5), p.917-923

1995

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The role of prostaglandins and allied substances in uterine haemostasis

Contraception (Stoneham), 1987-07, Vol.36 (1), p.23-35

Hagenfeldt, Kerstin

1987

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Ethics and family planning

Advances in contraception, 1991-06, Vol.7 (2-3), p.159-163

HAGENFELDT, K

1991

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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, Vol.58 (4), p.188-195

2002

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Fertility and pregnancy outcome in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Reply: The sex ratio of offspring of women with congenital adrenal hyperplasia

A 31-year-old woman with infertility and polycystic ovaries diagnosed with non-classic congenital adrenal hyperplasia due to a novel CYP21 mutation

Molecular targets of a human HNF1α mutation responsible for pancreatic β-cell dysfunction

The experience of women living with Congenital Adrenal Hyperplasia: impact of the condition and the care given

Gender Role Behavior, Sexuality, and Psychosocial Adaptation in Women with Congenital Adrenal Hyperplasia due to CYP21A2 Deficiency

Identity, Sexuality, and Parenthood in Women with Congenital Adrenal Hyperplasia

Ovarian epithelial neoplasia after hormonal infertility treatment: long-term follow-up of a historical cohort in Sweden

Sexual Function and Surgical Outcome in Women with Congenital Adrenal Hyperplasia Due to CYP21A2 Deficiency: Clinical Perspective and the Patients’ Perception

Type of Mutation and Surgical Procedure Affect Long-Term Quality of Life for Women with Congenital Adrenal Hyperplasia

Fractures and Bone Mineral Density in Adult Women with 21-Hydroxylase Deficiency

Metabolic Profile and Body Composition in Adult Women with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Voice problems due to virilization in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Prospective follow-up of menstrual disorders in adolescence and prognostic factors

Voice characteristics in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

A nutrition study in juvenile elite gymnasts

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

Bone mineral content of young female former gymnasts

Increased Liver Enzymes in Adult Women with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Menstrual disorders and associated factors among adolescent girls visiting a youth clinic

Reduced bone mineral density in adult women diagnosed with menstrual disorders during adolescence

Cotreatment with growth hormone and gonadotropin for ovulation induction in hypogonadotropic patients: a prospective, randomized, placebo-controlled, dose-response study

The role of prostaglandins and allied substances in uterine haemostasis

Ethics and family planning

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

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