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Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey

Clinical endocrinology (Oxford), 2011-12, Vol.75 (6), p.760-765

2011

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Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency

BMC pregnancy and childbirth, 2018-11, Vol.18 (1), p.456-456, Article 456

2018

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Quality of Survival and Growth in Children and Young Adults in the PNET4 European Controlled Trial of Hyperfractionated Versus Conventional Radiation Therapy for Standard-Risk Medulloblastoma

International journal of radiation oncology, biology, physics, 2014-02, Vol.88 (2), p.292-300

2014

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Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency

Journal of clinical research in pediatric endocrinology, 2019-03, Vol.11 (1), p.41-45

2019

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Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

BMC endocrine disorders, 2018-06, Vol.18 (1), p.37-37, Article 37

2018

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Adrenarche and pubarche in girls with turner syndrome during growth-promoting therapy with human growth hormone

BMC endocrine disorders, 2019-01, Vol.19 (1), p.9-9, Article 9

2019

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Genotyp-Phänotyp-Korrelation bei Zwillingsmädchen mit nichtklassischem adrenogenitalem Syndrom und 21-Hydroxylase-Defekt

Gynäkologische Endokrinologie, 2020-05, Vol.18 (2), p.123-128

2020

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Simultaneously reduced gene expression of cortisol-activating and cortisol-inactivating enzymes in placentas of small-for-gestational-age neonates

American journal of obstetrics and gynecology, 2007-07, Vol.197 (1), p.43.e1-43.e6

2007

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Intrauterine growth restriction (IUGR) is associated with increased leptin synthesis and binding capability in neonates

Clinical endocrinology (Oxford), 2011-04, Vol.74 (4), p.459-466

2011

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Altered 24-Hour Blood Pressure Profiles in Children and Adolescents with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2006-12, Vol.91 (12), p.4888-4895

2006

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Impact of Newborn Screening on Adult Height in Patients With Congenital Adrenal Hyperplasia (CAH)

The journal of clinical endocrinology and metabolism, 2023-11, Vol.108 (11), p.e1199-e1204

2023

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Carboxyl-Terminal Mutations in 3β-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2008-04, Vol.93 (4), p.1418-1425

2008

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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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Short-term adverse effects of testosterone used for priming in prepubertal boys before growth hormone stimulation test

Journal of Pediatric Endocrinology and Metabolism, 2018-01, Vol.31 (1), p.21-24

2018

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Automated, fast and sensitive quantification of 17α-hydroxy-progesterone, androstenedione and testosterone by tandem mass spectrometry with on-line extraction

Steroids, 2006-06, Vol.71 (6), p.450-458

2006

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Spontaneous postnatal growth is reduced in children with CHARGE syndrome

Acta Paediatrica, 2015-07, Vol.104 (7), p.e314-e318

2015

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Two novel mutations in the human thyroid peroxidase (TPO) gene: genetics and clinical findings in four children

Acta Paediatrica, 2009-06, Vol.98 (6), p.1057-1061

2009

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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-e105

2006

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Differential effects of low birthweight and intrauterine growth restriction on umbilical cord blood insulin-like growth factor concentrations

Clinical endocrinology (Oxford), 2015-11, Vol.83 (5), p.739-745

2015

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Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled Trial

Hormone research in paediatrics, 2015-01, Vol.84 (4), p.266-274

2015

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Short Children with CHARGE Syndrome: Do They Benefit from Growth Hormone Therapy?

Hormone research in paediatrics, 2015-01, Vol.84 (1), p.49-53

2015

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Hypergonadotropic hypogonadism and renal failure due to WT1 mutation

Nephrology, dialysis, transplantation, 2006-06, Vol.21 (6), p.1716-1718

2006

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Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Hormone research in paediatrics, 2011-01, Vol.76 (6), p.400-410

2011

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Lang wirksames Wachstumshormon – eine neue Therapieoption für Kinder mit Wachstumshormonmangel: Status 2024

Monatsschrift Kinderheilkunde, 2024-08

2024

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Different relationships between the first 2 years on growth hormone treatment and the d3-growth hormone receptor polymorphism in short small-for-gestational-age (SGA) children

Clinical endocrinology (Oxford), 2011-11, Vol.75 (5), p.656-660

2011

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Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey

Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency

Quality of Survival and Growth in Children and Young Adults in the PNET4 European Controlled Trial of Hyperfractionated Versus Conventional Radiation Therapy for Standard-Risk Medulloblastoma

Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

Adrenarche and pubarche in girls with turner syndrome during growth-promoting therapy with human growth hormone

Genotyp-Phänotyp-Korrelation bei Zwillingsmädchen mit nichtklassischem adrenogenitalem Syndrom und 21-Hydroxylase-Defekt

Simultaneously reduced gene expression of cortisol-activating and cortisol-inactivating enzymes in placentas of small-for-gestational-age neonates

Intrauterine growth restriction (IUGR) is associated with increased leptin synthesis and binding capability in neonates

Altered 24-Hour Blood Pressure Profiles in Children and Adolescents with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Impact of Newborn Screening on Adult Height in Patients With Congenital Adrenal Hyperplasia (CAH)

Carboxyl-Terminal Mutations in 3β-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia

Klinefelter syndrome and mediastinal germ cell tumors

Short-term adverse effects of testosterone used for priming in prepubertal boys before growth hormone stimulation test

Automated, fast and sensitive quantification of 17α-hydroxy-progesterone, androstenedione and testosterone by tandem mass spectrometry with on-line extraction

Spontaneous postnatal growth is reduced in children with CHARGE syndrome

Two novel mutations in the human thyroid peroxidase (TPO) gene: genetics and clinical findings in four children

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

Differential effects of low birthweight and intrauterine growth restriction on umbilical cord blood insulin-like growth factor concentrations

Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled Trial

Short Children with CHARGE Syndrome: Do They Benefit from Growth Hormone Therapy?

Hypergonadotropic hypogonadism and renal failure due to WT1 mutation

Adrenarche and Puberty in Children with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Lang wirksames Wachstumshormon – eine neue Therapieoption für Kinder mit Wachstumshormonmangel: Status 2024

Different relationships between the first 2 years on growth hormone treatment and the d3-growth hormone receptor polymorphism in short small-for-gestational-age (SGA) children

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