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Effects of Dehydroepiandrosterone Therapy on Pubic Hair Growth and Psychological Well-Being in Adolescent Girls and Young Women with Central Adrenal Insufficiency: A Double-Blind, Randomized, Placebo-Controlled Phase III Trial

The journal of clinical endocrinology and metabolism, 2009-04, Vol.94 (4), p.1182-1190

2009

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Impact of overweight on effectiveness of treatment with human growth hormone in growth hormone deficient children: analysis of German KIGS data

Experimental and clinical endocrinology & diabetes, 2011-10, Vol.119 (9), p.544

2011

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Is the response to growth hormone in short children born small for gestational age dependent on genetic or maternal factors?

Hormone research, 2009-01, Vol.72 (2), p.106-113

2009

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Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype

Annals of neurology, 1996-08, Vol.40 (2), p.254-257

1996

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Growth of heterokaryotic monozygotic twins discordant for Ullrich–Turner syndrome during the first years of life

American journal of medical genetics, 2004-04, Vol.126A (1), p.78-83

2004

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Tall stature as presenting symptom in a girl with triple X syndrome

Journal of pediatric endocrinology & metabolism : JPEM, 2003-02, Vol.16 (2), p.233

2003

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Effects of Dehydroepiandrosterone Therapy on Pubic Hair Growth and Psychological Well-Being in Adolescent Girls and Young Women with Central Adrenal Insufficiency: A Double-Blind, Randomised, Placebo-Controlled Phase III Trial

Endocrinology (Philadelphia), 2009-02, Vol.150 (2), p.1070-1070

2009

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Radiation therapy of optico–hypothalamic gliomas (OHG) – radiographic response, vision and late toxicity

Radiotherapy and oncology, 2000-03, Vol.54 (3), p.239-245

2000

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First-year predictors of health-related quality of life changes in short-statured children treated with human growth hormone

Journal of endocrinological investigation, 2019-09, Vol.42 (9), p.1067-1076

2019

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Growth hormone deficiency in one of two siblings with Fanconi’s anaemia complementation group FA-D

Growth hormone & IGF research, 2000-10, Vol.10 (5), p.290-293

2000

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SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome

Journal of medical genetics, 2007-10, Vol.44 (10), p.651-656

2007

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Developmental patterns of serum 3α-androstanediol glucuronide

Journal of endocrinological investigation, 1997-05, Vol.20 (5), p.245-250

1997

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Observations of reported and measured heights of mothers of short statured children

Annals of human biology, 1998-07, Vol.25 (4), p.387-390

1998

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Developmental patterns of serum 3α-androstanediol glucuronide

Journal of endocrinological investigation, 1997-03, Vol.20 (3), p.138-143

1997

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Größenwachstum und Knochengesundheit bei Erkrankungen der Wachstumsfuge und des Knochens: Möglichkeiten und Grenzen einer GH-Therapie

Monatsschrift Kinderheilkunde, 2024-05, Vol.172 (5), p.426-436

2024

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Glukokortikoide bei nichtendokrinen Erkrankungen, bei Kortisolmangel und bei endogenem Exzess – der Einfluss therapeutischer Strategien auf das kindliche Wachstum

Monatsschrift Kinderheilkunde, 2021-11, Vol.169 (11), p.1051-1058

2021

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Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase-Deficiency: 13 Years of Neonatal Screening and Follow-up in Bavaria

Klinische Padiatrie, 2015-09, Vol.227 (5), p.278

2015

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Mania in a Girl with Cushing's Disease

Journal of the American Academy of Child and Adolescent Psychiatry, 1989-07, Vol.28 (4), p.610-611

1989

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Plasma mineralocorticoids, glucocorticoids, and progestins in premature infants: longitudinal study during the first week of life

Pediatric research, 1988-05, Vol.23 (5), p.525-529

1988

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ACTH and multisteroid responses to corticotropin-releasing factor in depressive illness: Relationship to multisteroid responses after ACTH stimulation and dexamethasone suppression

Psychoneuroendocrinology, 1984, Vol.9 (2), p.147-160

1984

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Naltrexone as a diagnostic tool to distinguish between hyperandrogenemic and hypothalamic ovarian failure in females with congenital adrenal hyperplasia due to 21-hydroxylase-deficiency (CAH)

European journal of obstetrics & gynecology and reproductive biology, 2014-09, Vol.180, p.153-156

2014

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Genotype-phenotype correlations in Noonan syndrome

The Journal of pediatrics, 2004-03, Vol.144 (3), p.368-374

2004

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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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The VCUAM (Vagina Cervix Uterus Adnex–associated Malformation) Classification: a new classification for genital malformations

Fertility and sterility, 2005-11, Vol.84 (5), p.1493-1497

2005

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Expertsʼ Opinion on the Prenatal Therapy of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency – Guideline of DGKED in cooperation with DGGG (S1-Level, AWMF Registry No. 174/013, July 2015)

Geburtshilfe und Frauenheilkunde, 2015-12, Vol.75 (12), p.1232-1238

2015

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Effects of Dehydroepiandrosterone Therapy on Pubic Hair Growth and Psychological Well-Being in Adolescent Girls and Young Women with Central Adrenal Insufficiency: A Double-Blind, Randomized, Placebo-Controlled Phase III Trial

Impact of overweight on effectiveness of treatment with human growth hormone in growth hormone deficient children: analysis of German KIGS data

Is the response to growth hormone in short children born small for gestational age dependent on genetic or maternal factors?

Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype

Growth of heterokaryotic monozygotic twins discordant for Ullrich–Turner syndrome during the first years of life

Tall stature as presenting symptom in a girl with triple X syndrome

Effects of Dehydroepiandrosterone Therapy on Pubic Hair Growth and Psychological Well-Being in Adolescent Girls and Young Women with Central Adrenal Insufficiency: A Double-Blind, Randomised, Placebo-Controlled Phase III Trial

Radiation therapy of optico–hypothalamic gliomas (OHG) – radiographic response, vision and late toxicity

First-year predictors of health-related quality of life changes in short-statured children treated with human growth hormone

Growth hormone deficiency in one of two siblings with Fanconi’s anaemia complementation group FA-D

SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome

Developmental patterns of serum 3α-androstanediol glucuronide

Observations of reported and measured heights of mothers of short statured children

Developmental patterns of serum 3α-androstanediol glucuronide

Größenwachstum und Knochengesundheit bei Erkrankungen der Wachstumsfuge und des Knochens: Möglichkeiten und Grenzen einer GH-Therapie

Glukokortikoide bei nichtendokrinen Erkrankungen, bei Kortisolmangel und bei endogenem Exzess – der Einfluss therapeutischer Strategien auf das kindliche Wachstum

Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase-Deficiency: 13 Years of Neonatal Screening and Follow-up in Bavaria

Mania in a Girl with Cushing's Disease

Plasma mineralocorticoids, glucocorticoids, and progestins in premature infants: longitudinal study during the first week of life

ACTH and multisteroid responses to corticotropin-releasing factor in depressive illness: Relationship to multisteroid responses after ACTH stimulation and dexamethasone suppression

Naltrexone as a diagnostic tool to distinguish between hyperandrogenemic and hypothalamic ovarian failure in females with congenital adrenal hyperplasia due to 21-hydroxylase-deficiency (CAH)

Genotype-phenotype correlations in Noonan syndrome

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

The VCUAM (Vagina Cervix Uterus Adnex–associated Malformation) Classification: a new classification for genital malformations

Expertsʼ Opinion on the Prenatal Therapy of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency – Guideline of DGKED in cooperation with DGGG (S1-Level, AWMF Registry No. 174/013, July 2015)

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