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Acceleration of BMI in Early Childhood and Risk of Sustained Obesity

The New England journal of medicine, 2018-10, Vol.379 (14), p.1303-1312

2018

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Age- and weight group-specific weight gain patterns in children and adolescents during the 15 years before and during the COVID-19 pandemic

International Journal of Obesity, 2022-01, Vol.46 (1), p.144-152

2022

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Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation

Nature communications, 2018-05, Vol.9 (1), p.2105-10, Article 2105

2018

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Early Growth Hormone Initiation Leads to Favorable Long-Term Growth Outcomes in Children Born Small for Gestational Age

The journal of clinical endocrinology and metabolism, 2023-05, Vol.108 (5), p.1043-1052

2023

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Hormone replacement therapy in children: The use of growth hormone and IGF-I

Baillière's best practice & research. Clinical endocrinology & metabolism, 2015-06, Vol.29 (3), p.339-352

Pfäffle, Roland, Prof. Dr. med., MD

2015

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Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

Journal of human genetics, 2017-08, Vol.62 (8), p.755-762

2017

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Genetics of Growth Disorders—Which Patients Require Genetic Testing?

Frontiers in endocrinology (Lausanne), 2019-09, Vol.10

2019

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A Comprehensive Cohort Analysis Comparing Growth and GH Therapy Response in IGF1R Mutation Carriers and SGA Children

The journal of clinical endocrinology and metabolism, 2020-04, Vol.105 (4), p.e1705-e1717

2020

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Effects of obesity on human sexual development

Nature reviews. Endocrinology, 2012-04, Vol.8 (4), p.246-254

2012

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Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes

EBioMedicine, 2018-10, Vol.36, p.390-400

2018

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Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency

Genetics in medicine, 2018-07, Vol.20 (7), p.728-736

2018

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Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation

The journal of clinical endocrinology and metabolism, 2010-03, Vol.95 (3), p.1137-1142

2010

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A Heterozygous Mutation of the Insulin-Like Growth Factor-I Receptor Causes Retention of the Nascent Protein in the Endoplasmic Reticulum and Results in Intrauterine and Postnatal Growth Retardation

The journal of clinical endocrinology and metabolism, 2010-05, Vol.95 (5), p.2316-2324

2010

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IGF signaling defects as causes of growth failure and IUGR

Trends in endocrinology and metabolism, 2008-08, Vol.19 (6), p.197-205

2008

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Growth hormone treatment in children with Prader-Willi syndrome: safety and effectiveness data from the PATRO Children study

Therapeutic advances in endocrinology and metabolism, 2024, Vol.15, p.20420188241264343

2024

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Growth Hormone Treatment for Short Stature in the USA, Germany and France: 15 Years of Surveillance in the Genetics and Neuroendocrinology of Short-Stature International Study (GeNeSIS)

Hormone research in paediatrics, 2018-01, Vol.90 (3), p.169-180

2018

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A novel FoxD3 Variant Is Associated With Vitiligo and Elevated Thyroid Auto-Antibodies

The journal of clinical endocrinology and metabolism, 2015-10, Vol.100 (10), p.E1335-E1342

2015

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Germline NF1 Mutational Spectra and Loss-of-Heterozygosity Analyses in Patients with Pheochromocytoma and Neurofibromatosis Type 1

The journal of clinical endocrinology and metabolism, 2007-07, Vol.92 (7), p.2784-2792

2007

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Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference values

EClinicalMedicine, 2021-07, Vol.37, p.100977-100977, Article 100977

2021

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PROP1 Mutations Cause Progressive Deterioration of Anterior Pituitary Function including Adrenal Insufficiency: A Longitudinal Analysis

The journal of clinical endocrinology and metabolism, 2004-10, Vol.89 (10), p.5256-5265

2004

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Influence of seasonal variation on blood pressure measurements in children, adolescents and young adults

Pediatric nephrology (Berlin, West), 2013-12, Vol.28 (12), p.2343-2349

2013

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Associations between Pituitary Imaging Abnormalities and Clinical and Biochemical Phenotypes in Children with Congenital Growth Hormone Deficiency: Data from an International Observational Study

Hormone research in paediatrics, 2013-01, Vol.79 (5), p.283-292

2013

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Blood pressure tracking in children and adolescents

Pediatric nephrology (Berlin, West), 2013-12, Vol.28 (12), p.2351-2359

2013

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Roles of the LHX3 and LHX4 LIM-homeodomain factors in pituitary development

Molecular and cellular endocrinology, 2007-02, Vol.265-266, p.190-195

2007

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IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA)

Open access Macedonian journal of medical sciences, 2018-11, Vol.6 (11), p.2040-2044

2018

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Acceleration of BMI in Early Childhood and Risk of Sustained Obesity

Age- and weight group-specific weight gain patterns in children and adolescents during the 15 years before and during the COVID-19 pandemic

Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation

Early Growth Hormone Initiation Leads to Favorable Long-Term Growth Outcomes in Children Born Small for Gestational Age

Hormone replacement therapy in children: The use of growth hormone and IGF-I

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

Genetics of Growth Disorders—Which Patients Require Genetic Testing?

A Comprehensive Cohort Analysis Comparing Growth and GH Therapy Response in IGF1R Mutation Carriers and SGA Children

Effects of obesity on human sexual development

Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes

Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency

Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation

A Heterozygous Mutation of the Insulin-Like Growth Factor-I Receptor Causes Retention of the Nascent Protein in the Endoplasmic Reticulum and Results in Intrauterine and Postnatal Growth Retardation

IGF signaling defects as causes of growth failure and IUGR

Growth hormone treatment in children with Prader-Willi syndrome: safety and effectiveness data from the PATRO Children study

Growth Hormone Treatment for Short Stature in the USA, Germany and France: 15 Years of Surveillance in the Genetics and Neuroendocrinology of Short-Stature International Study (GeNeSIS)

A novel FoxD3 Variant Is Associated With Vitiligo and Elevated Thyroid Auto-Antibodies

Germline NF1 Mutational Spectra and Loss-of-Heterozygosity Analyses in Patients with Pheochromocytoma and Neurofibromatosis Type 1

Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference values

PROP1 Mutations Cause Progressive Deterioration of Anterior Pituitary Function including Adrenal Insufficiency: A Longitudinal Analysis

Influence of seasonal variation on blood pressure measurements in children, adolescents and young adults

Associations between Pituitary Imaging Abnormalities and Clinical and Biochemical Phenotypes in Children with Congenital Growth Hormone Deficiency: Data from an International Observational Study

Blood pressure tracking in children and adolescents

Roles of the LHX3 and LHX4 LIM-homeodomain factors in pituitary development

IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA)

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