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17-Alpha Hydroxylase Deficiency: A Rare Case of Primary Amenorrhea and Hypertension

Turkish Journal of Endocrinology and Metabolism, 2014-01, Vol.18 (4), p.137-139

2014

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46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the HSD17B3 Gene

Sexual development, 2014-01, Vol.8 (4), p.151-155

2014

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The A645D Mutation in the Hinge Region of the Human Androgen Receptor (AR) Gene Modulates AR Activity, Depending on the Context of the Polymorphic Glutamine and Glycine Repeats

The journal of clinical endocrinology and metabolism, 2006-09, Vol.91 (9), p.3515-3520

2006

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The Action of Reproductive Fluids and Contained Steroids, Prostaglandins, and Zn2+ on CatSper Ca2+ Channels in Human Sperm

Frontiers in cell and developmental biology, 2021-07, Vol.9, p.699554-699554

2021

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Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism

Dermato-endocrinology, 2012-01, Vol.4 (1), p.58-64

2012

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Age at menarche relates to depression in adolescent girls: Comparing a clinical sample to the general pediatric population

Journal of affective disorders, 2022-12, Vol.318, p.103-112

2022

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The Aldosterone/Renin Ratio as a Diagnostic Tool for the Diagnosis of Primary Hypoaldosteronism in Newborns and Infants

Hormone research in paediatrics, 2015-01, Vol.84 (1), p.43-48

2015

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Analyzing the Functional and Structural Consequences of Two Point Mutations (P94L and A368D) in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia Resulting from 11-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2006-07, Vol.91 (7), p.2682-2688

2006

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Androgen action

Endocrine development, 2014, Vol.27, p.28

2014

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Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructs

The Journal of steroid biochemistry and molecular biology, 2006-09, Vol.101 (1), p.1-10

2006

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Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndrome

Journal of molecular medicine (Berlin, Germany), 2009-06, Vol.87 (6), p.623-632

2009

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Area Deprivation and Regional Disparities in Treatment and Outcome Quality of 29,284 Pediatric Patients With Type 1 Diabetes in Germany: A Cross-sectional Multicenter DPV Analysis

Diabetes care, 2018-12, Vol.41 (12), p.2517-2525

2018

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The basis of gender assignment in disorders of somatosexual differentiation

Hormone research, 2005-01, Vol.64 Suppl 2 (Suppl. 2), p.18-22

2005

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Behavior and circadian glucocorticoids in prepubertal monozygotic twins with birthweight differences: A prospective longitudinal cohort study on twin-to-twin transfusion syndrome patients

Psychoneuroendocrinology, 2024-09, Vol.167, p.107082, Article 107082

2024

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Biological characterization of adult MYC-translocation-positive mature B-cell lymphomas other than molecular Burkitt lymphoma

Haematologica (Roma), 2014-04, Vol.99 (4), p.726-735

2014

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Birth Weight in Different Etiologies of Disorders of Sex Development

The journal of clinical endocrinology and metabolism, 2017-03, Vol.102 (3), p.1044-1050

2017

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Cell-line and tissue-specific signatures of androgen receptor-coregulator transcription

Journal of molecular medicine (Berlin, Germany), 2006-11, Vol.84 (11), p.919-931

2006

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Changes over time in sex assignment for disorders of sex development

Pediatrics (Evanston), 2014-09, Vol.134 (3), p.e710-e715

2014

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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.697-706

2014

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Chronic recurrent multifocal osteomyelitis in children

The Pediatric infectious disease journal, 1999-11, Vol.18 (11), p.1008-1013

1999

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Classic genetic and hormonal switches during fetal sex development and beyond

Medizinische Genetik, 2023-09, Vol.35 (3), p.163-171

2023

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Classification of Distinct Baseline Insulin Infusion Patterns in Children and Adolescents With Type 1 Diabetes on Continuous Subcutaneous Insulin Infusion Therapy

Diabetes care, 2007-03, Vol.30 (3), p.568-573

2007

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The clinical and molecular spectrum of androgen insensitivity syndromes

American journal of medical genetics, 1996-05, Vol.63 (1), p.218-222

1996

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Clinical and molecular spectrum of somatic mosaicism in androgen insensitivity syndrome

Pediatric research, 1999-12, Vol.46 (6), p.684-690

1999

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Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis

The journal of clinical endocrinology and metabolism, 2019-10, Vol.104 (10), p.4366-4381

2019

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17-Alpha Hydroxylase Deficiency: A Rare Case of Primary Amenorrhea and Hypertension

46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the HSD17B3 Gene

The A645D Mutation in the Hinge Region of the Human Androgen Receptor (AR) Gene Modulates AR Activity, Depending on the Context of the Polymorphic Glutamine and Glycine Repeats

The Action of Reproductive Fluids and Contained Steroids, Prostaglandins, and Zn2+ on CatSper Ca2+ Channels in Human Sperm

Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism

Age at menarche relates to depression in adolescent girls: Comparing a clinical sample to the general pediatric population

The Aldosterone/Renin Ratio as a Diagnostic Tool for the Diagnosis of Primary Hypoaldosteronism in Newborns and Infants

Analyzing the Functional and Structural Consequences of Two Point Mutations (P94L and A368D) in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia Resulting from 11-Hydroxylase Deficiency

Androgen action

Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructs

Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndrome

Area Deprivation and Regional Disparities in Treatment and Outcome Quality of 29,284 Pediatric Patients With Type 1 Diabetes in Germany: A Cross-sectional Multicenter DPV Analysis

The basis of gender assignment in disorders of somatosexual differentiation

Behavior and circadian glucocorticoids in prepubertal monozygotic twins with birthweight differences: A prospective longitudinal cohort study on twin-to-twin transfusion syndrome patients

Biological characterization of adult MYC-translocation-positive mature B-cell lymphomas other than molecular Burkitt lymphoma

Birth Weight in Different Etiologies of Disorders of Sex Development

Cell-line and tissue-specific signatures of androgen receptor-coregulator transcription

Changes over time in sex assignment for disorders of sex development

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

Chronic recurrent multifocal osteomyelitis in children

Classic genetic and hormonal switches during fetal sex development and beyond

Classification of Distinct Baseline Insulin Infusion Patterns in Children and Adolescents With Type 1 Diabetes on Continuous Subcutaneous Insulin Infusion Therapy

The clinical and molecular spectrum of androgen insensitivity syndromes

Clinical and molecular spectrum of somatic mosaicism in androgen insensitivity syndrome

Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis

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