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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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A 31-year-old woman with infertility and polystic 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

2008

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Pdx1 Level Defines Pancreatic Gene Expression Pattern and Cell Lineage Differentiation

The Journal of biological chemistry, 2001-07, Vol.276 (27), p.25279-25286

2001

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Hepatocyte Nuclear Factor 4α Regulates the Expression of Pancreatic β-Cell Genes Implicated in Glucose Metabolism and Nutrient-induced Insulin Secretion

The Journal of biological chemistry, 2000-11, Vol.275 (46), p.35953-35959

2000

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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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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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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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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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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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Use of evidence in WHO recommendations

The Lancet (British edition), 2007-09, Vol.370 (9590), p.825-825

2007

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A new report on osteoporosis coming soon. The SBU evaluates prevention, diagnosis and treatment

Läkartidningen, 2002-02, Vol.99 (9), p.874-874

Hagenfeldt, Kerstin

2002

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Dominant-negative suppression of HNF-1α function results in defective insulin gene transcription and impaired metabolism-secretion coupling in a pancreatic β-cell line

The EMBO journal, 1998-11, Vol.17 (22), p.6701-6713

1998

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Adrenogenital syndrome in children and adolescents--new guidelines for treatment. An international consensus conference emphasizes the need of team work

Läkartidningen, 2003, Vol.100 (18), p.1626

2003

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Foxa2 (HNF3β) Controls Multiple Genes Implicated in Metabolism-Secretion Coupling of Glucose-induced Insulin Release

The Journal of biological chemistry, 2002-05, Vol.277 (20), p.17564-17570

2002

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The transcription factor SREBP-1c is instrumental in the development of beta-cell dysfunction

The Journal of biological chemistry, 2003-05, Vol.278 (19), p.16622-16629

2003

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β-Cell-Targeted Expression of a Dominant-Negative Hepatocyte Nuclear Factor-1α Induces a Maturity-Onset Diabetes of the Young (MODY)3-Like Phenotype in Transgenic Mice

Endocrinology (Philadelphia), 2001-12, Vol.142 (12), p.5311-5320

2001

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Evidence provides a safer basis in health care--neither more nor less

Läkartidningen, 2006, Vol.103 (1-2), p.7-8

2006

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Adrenogenital syndrome in children and adolescents--new guidelines for treatment. An international consensus conference emphasizes the need of team work

Läkartidningen, 2003-04, Vol.100 (18), p.1626-1629

2003

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The modes of action of medicated intrauterine devices

Journal of reproduction and fertility. Supplement, 1976-10 (25), p.117

Hagenfeldt, K

1976

Volltextzugriff (PDF)

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency – the adult woman

Growth hormone & IGF research, 2004-06, Vol.14, p.67-71

Hagenfeldt, Kerstin B.

2004

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Studies on the mode of action of the Copper-T device

Acta endocrinologica. Supplementum, 1972, Vol.169, p.3

Hagenfeldt, K

1972

Volltextzugriff (PDF)

Experimental Models of Transcription Factor-Associated Maturity-Onset Diabetes of the Young

Diabetes (New York, N.Y.), 2002-12, Vol.51 (suppl 3), p.S333-S342

2002

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Influence of contraceptive steroids on the turnover of plasma free arachidonic and oleic acids

Hormone and metabolic research, 1977-01, Vol.9 (1), p.66-69

1977

Volltextzugriff (PDF)

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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

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

Pdx1 Level Defines Pancreatic Gene Expression Pattern and Cell Lineage Differentiation

Hepatocyte Nuclear Factor 4α Regulates the Expression of Pancreatic β-Cell Genes Implicated in Glucose Metabolism and Nutrient-induced Insulin Secretion

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

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

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

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

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

Use of evidence in WHO recommendations

A new report on osteoporosis coming soon. The SBU evaluates prevention, diagnosis and treatment

Dominant-negative suppression of HNF-1α function results in defective insulin gene transcription and impaired metabolism-secretion coupling in a pancreatic β-cell line

Adrenogenital syndrome in children and adolescents--new guidelines for treatment. An international consensus conference emphasizes the need of team work

Foxa2 (HNF3β) Controls Multiple Genes Implicated in Metabolism-Secretion Coupling of Glucose-induced Insulin Release

The transcription factor SREBP-1c is instrumental in the development of beta-cell dysfunction

β-Cell-Targeted Expression of a Dominant-Negative Hepatocyte Nuclear Factor-1α Induces a Maturity-Onset Diabetes of the Young (MODY)3-Like Phenotype in Transgenic Mice

Evidence provides a safer basis in health care--neither more nor less

Adrenogenital syndrome in children and adolescents--new guidelines for treatment. An international consensus conference emphasizes the need of team work

The modes of action of medicated intrauterine devices

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency – the adult woman

Studies on the mode of action of the Copper-T device

Experimental Models of Transcription Factor-Associated Maturity-Onset Diabetes of the Young

Influence of contraceptive steroids on the turnover of plasma free arachidonic and oleic acids

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