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A Novel Ultrapressure Liquid Chromatography Tandem Mass Spectrometry Method for the Simultaneous Determination of Androstenedione, Testosterone, and Dihydrotestosterone in Pediatric Blood Samples: Age- and Sex-Specific Reference Data

The journal of clinical endocrinology and metabolism, 2010-05, Vol.95 (5), p.2399-2409

2010

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Androgen receptor function links human sexual dimorphism to DNA methylation

PloS one, 2013-09, Vol.8 (9), p.e73288-e73288

2013

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Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation - A Case Report and Review of the Literature: Implications for the Pathomechanism

Hormone research in paediatrics, 2019, Vol.91 (5), p.336-345

2019

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In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humans

PloS one, 2015-03, Vol.10 (3), p.e0120463

2015

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Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

Genes & development, 2003-03, Vol.17 (6), p.711-716

2003

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Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Reviews in endocrine & metabolic disorders, 2007-12, Vol.8 (4), p.349-363

2007

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Duplication of The SOX3 Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the Literature

Balkan journal of medical genetics, 2019-08, Vol.22 (1), p.81-88

2019

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Frequency and characterization of DNA methylation defects in children born SGA

European journal of human genetics : EJHG, 2013-08, Vol.21 (8), p.838-843

2013

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CYP17A1 intron mutation causing cryptic splicing in 17α-hydroxylase deficiency

PloS one, 2011-09, Vol.6 (9), p.e25492

2011

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Classification of Wounds at Risk and Their Antimicrobial Treatment with Polihexanide: A Practice-Oriented Expert Recommendation

Skin pharmacology and physiology, 2011-01, Vol.24 (5), p.245-255

2011

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What can we Learn from Explanted Endovascular Devices?

European journal of vascular and endovascular surgery, 2002-08, Vol.24 (2), p.117-122

2002

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No Correlation between Androgen Receptor CAG and GGN Repeat Length and the Degree of Genital Virilization in Females with 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2010-05, Vol.95 (5), p.2443-2450

2010

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Implementation of a Liquid Chromatography Tandem Mass Spectrometry Assay for Eight Adrenal C-21 Steroids and Pediatric Reference Data

Hormone research in paediatrics, 2013-01, Vol.79 (1), p.22-31

2013

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Corroded Nitinol Wires in Explanted Aortic Endografts: An Important Mechanism of Failure?

Journal of endovascular therapy, 2001-06, Vol.8 (3), p.248-253

2001

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Homozygous Disruption of P450 Side-Chain Cleavage (CYP11A1) Is Associated with Prematurity, Complete 46,XY Sex Reversal, and Severe Adrenal Failure

The journal of clinical endocrinology and metabolism, 2005-01, Vol.90 (1), p.538-541

2005

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Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

European journal of human genetics : EJHG, 2020-05, Vol.28 (5), p.692-692

2020

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Four Novel Missense Mutations in the CYP21A2 Gene Detected in Russian Patients Suffering from the Classical Form of Congenital Adrenal Hyperplasia: Identification, Functional Characterization, and Structural Analysis

The journal of clinical endocrinology and metabolism, 2006-12, Vol.91 (12), p.4976-4980

2006

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A practice-oriented recommendation for treatment of critically colonised and locally infected wounds using polihexanide

Journal of tissue viability, 2010-08, Vol.19 (3), p.106-115

2010

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Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

European journal of human genetics : EJHG, 2014-05, Vol.22 (5), p.610-616

2014

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LC-MS/MS based determination of basal- and ACTH-stimulated plasma concentrations of 11 steroid hormones: implications for detecting heterozygote CYP21A2 mutation carriers

European journal of endocrinology, 2015-10, Vol.173 (4), p.517

2015

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Characterisation of three novel CYP11B1 mutations in classic and non-classic 11β-hydroxylase deficiency

European journal of endocrinology, 2014-05, Vol.170 (5), p.697

2014

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Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in the CYP11B1 Gene

The journal of clinical endocrinology and metabolism, 2005-06, Vol.90 (6), p.3724-3730

2005

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Congenital adrenal hyperplasia - how to improve the transition from adolescence to adult life

Experimental and clinical endocrinology & diabetes, 2004-07, Vol.112 (7), p.343

2004

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Hashimoto Encephalopathy in a 15-Year-Old-Girl: EEG Findings and Follow-Up

Pediatric neurology, 2009-10, Vol.41 (4), p.301-304

2009

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Adrenal gland: Congenital adrenal hyperplasia: new treatment guidelines

Nature reviews. Endocrinology, 2011-01, Vol.7 (1), p.6

Riepe, Felix G

2011

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A Novel Ultrapressure Liquid Chromatography Tandem Mass Spectrometry Method for the Simultaneous Determination of Androstenedione, Testosterone, and Dihydrotestosterone in Pediatric Blood Samples: Age- and Sex-Specific Reference Data

Androgen receptor function links human sexual dimorphism to DNA methylation

Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation - A Case Report and Review of the Literature: Implications for the Pathomechanism

In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humans

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Duplication of The SOX3 Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the Literature

Frequency and characterization of DNA methylation defects in children born SGA

CYP17A1 intron mutation causing cryptic splicing in 17α-hydroxylase deficiency

Classification of Wounds at Risk and Their Antimicrobial Treatment with Polihexanide: A Practice-Oriented Expert Recommendation

What can we Learn from Explanted Endovascular Devices?

No Correlation between Androgen Receptor CAG and GGN Repeat Length and the Degree of Genital Virilization in Females with 21-Hydroxylase Deficiency

Implementation of a Liquid Chromatography Tandem Mass Spectrometry Assay for Eight Adrenal C-21 Steroids and Pediatric Reference Data

Corroded Nitinol Wires in Explanted Aortic Endografts: An Important Mechanism of Failure?

Homozygous Disruption of P450 Side-Chain Cleavage (CYP11A1) Is Associated with Prematurity, Complete 46,XY Sex Reversal, and Severe Adrenal Failure

Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

Four Novel Missense Mutations in the CYP21A2 Gene Detected in Russian Patients Suffering from the Classical Form of Congenital Adrenal Hyperplasia: Identification, Functional Characterization, and Structural Analysis

A practice-oriented recommendation for treatment of critically colonised and locally infected wounds using polihexanide

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

LC-MS/MS based determination of basal- and ACTH-stimulated plasma concentrations of 11 steroid hormones: implications for detecting heterozygote CYP21A2 mutation carriers

Characterisation of three novel CYP11B1 mutations in classic and non-classic 11β-hydroxylase deficiency

Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in the CYP11B1 Gene

Congenital adrenal hyperplasia - how to improve the transition from adolescence to adult life

Hashimoto Encephalopathy in a 15-Year-Old-Girl: EEG Findings and Follow-Up

Adrenal gland: Congenital adrenal hyperplasia: new treatment guidelines

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