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Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

European journal of endocrinology, 2022-05, Vol.186 (5), p.K17

2022

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Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Pediatrics (Evanston), 2006-01, Vol.117 (1), p.e98

2006

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Circadian Rhythm of Salivary Cortisol, 17α-Hydroxyprogesterone, and Progesterone in Healthy Children

Clinical chemistry (Baltimore, Md.), 2003-10, Vol.49 (10), p.1688-1691

2003

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Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21-hydroxylase deficiency in Europe

HORMONE RESEARCH IN PAEDIATRICS, 2021, Vol.94 (SUPPL 1), p.145

2021

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Stability of salivary steroids: the influences of storage, food and dental care

Steroids, 2001-10, Vol.66 (10), p.737-741

2001

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Rapid Second-Tier Molecular Genetic Analysis for Congenital Adrenal Hyperplasia Attributable to Steroid 21-Hydroxylase Deficiency

Clinical chemistry (Baltimore, Md.), 2005-02, Vol.51 (2), p.298-304

2005

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Klinefelter syndrome and mediastinal germ cell tumors

American journal of medical genetics. Part A, 2006-03, Vol.140A (5), p.471-481

2006

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Identification of leptin in human saliva

The journal of clinical endocrinology and metabolism, 2001-11, Vol.86 (11), p.5234-5239

2001

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Cardiovascular anomalies in children and young adults with Ullrich‐Turner syndrome—the erlangen experience

Clinical cardiology (Mahwah, N.J.), 2005-02, Vol.28 (2), p.88-92

2005

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Cortisol and 17-Hydroxyprogesterone Kinetics in Saliva after Oral Administration of Hydrocortisone in Children and Young Adolescents with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2002-03, Vol.87 (3), p.1200-1204

2002

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Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations

Journal of molecular medicine (Berlin, Germany), 2005-12, Vol.83 (12), p.1005-1013

2005

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Attempted suicide with L-thyroxine in an adolescent girl

Klinische Pädiatrie, 2006-01, Vol.218 (1), p.34-37

2006

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Profiling steroid hormones in amniotic fluid of midpregnancy by routine stable isotope dilution/gas chromatography-mass spectrometry : Reference values and concentrations in fetuses at risk for 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2724-2728

1999

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Adult height after GH therapy in 188 Ullrich-Turner syndrome patients: results of the German IGLU Follow-up Study 2001

European journal of endocrinology, 2002-11, Vol.147 (5), p.625

2002

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Relationship between salivary progesterone, 17-hydroxyprogesterone, and cortisol levels throughout the normal menstrual cycle of healthy postmenarcheal girls

Fertility and sterility, 2001-09, Vol.76 (3), p.615-617

2001

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Pediatric renal allograft transplantation does not normalize the increased cortisol/cortisone ratios of chronic renal failure

European journal of endocrinology, 2006-04, Vol.154 (4), p.555

2006

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Homocysteine concentrations in a German cohort of 500 individuals: reference ranges and determinants of plasma levels in healthy children and their parents

Amino acids, 2001-01, Vol.20 (4), p.409-418

2001

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Central reassessment of GH concentrations measured at local treatment centers in children with impaired growth: consequences for patient management

European journal of endocrinology, 2004-03, Vol.150 (3), p.291

2004

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Prospective Multicenter Registration of Major Late Sequelae in Sarcoma Patients Using the Late Effects Surveillance System (LESS)

Klinische Pädiatrie, 2005-05, Vol.217 (3), p.176-181

2005

Volltextzugriff (PDF)

Does growth hormone (GH) enhance growth in GH-deficient children with myelomeningocele?

The journal of clinical endocrinology and metabolism, 2000-08, Vol.85 (8), p.2740-2743

2000

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Growth and pubertal development in patients with meningomyelocele: a retrospective analysis

Acta Paediatrica, 1996-01, Vol.85 (1), p.76-80

1996

Volltextzugriff (PDF)

Growth failure in a girl with Fanconi syndrome and growth hormone deficiency

Nephrology, dialysis, transplantation, 2004-07, Vol.19 (7), p.1910-1912

2004

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A novel 5q35.3 subtelomeric deletion syndrome

American journal of medical genetics, 2003-08, Vol.121A (1), p.1-8

2003

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Craniopharyngioma in a Female Adolescent Presenting with Symptoms of Anorexia Nervosa

Klinische Pädiatrie, 2006-03, Vol.218 (2), p.67-71

2006

Volltextzugriff (PDF)

Serum cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy

Journal of endocrinological investigation, 2005-05, Vol.28 (5), p.413

2005

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Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Circadian Rhythm of Salivary Cortisol, 17α-Hydroxyprogesterone, and Progesterone in Healthy Children

Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21-hydroxylase deficiency in Europe

Stability of salivary steroids: the influences of storage, food and dental care

Rapid Second-Tier Molecular Genetic Analysis for Congenital Adrenal Hyperplasia Attributable to Steroid 21-Hydroxylase Deficiency

Klinefelter syndrome and mediastinal germ cell tumors

Identification of leptin in human saliva

Cardiovascular anomalies in children and young adults with Ullrich‐Turner syndrome—the erlangen experience

Cortisol and 17-Hydroxyprogesterone Kinetics in Saliva after Oral Administration of Hydrocortisone in Children and Young Adolescents with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations

Attempted suicide with L-thyroxine in an adolescent girl

Profiling steroid hormones in amniotic fluid of midpregnancy by routine stable isotope dilution/gas chromatography-mass spectrometry : Reference values and concentrations in fetuses at risk for 21-hydroxylase deficiency

Adult height after GH therapy in 188 Ullrich-Turner syndrome patients: results of the German IGLU Follow-up Study 2001

Relationship between salivary progesterone, 17-hydroxyprogesterone, and cortisol levels throughout the normal menstrual cycle of healthy postmenarcheal girls

Pediatric renal allograft transplantation does not normalize the increased cortisol/cortisone ratios of chronic renal failure

Homocysteine concentrations in a German cohort of 500 individuals: reference ranges and determinants of plasma levels in healthy children and their parents

Central reassessment of GH concentrations measured at local treatment centers in children with impaired growth: consequences for patient management

Prospective Multicenter Registration of Major Late Sequelae in Sarcoma Patients Using the Late Effects Surveillance System (LESS)

Does growth hormone (GH) enhance growth in GH-deficient children with myelomeningocele?

Growth and pubertal development in patients with meningomyelocele: a retrospective analysis

Growth failure in a girl with Fanconi syndrome and growth hormone deficiency

A novel 5q35.3 subtelomeric deletion syndrome

Craniopharyngioma in a Female Adolescent Presenting with Symptoms of Anorexia Nervosa

Serum cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy

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