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

The journal of clinical endocrinology and metabolism, 2023-10, Vol.108 (11), p.e1199-e1204

2023

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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

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

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

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

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

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

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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