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Felix G. Riepe
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Journal Articles

Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation – A Case Report and Review of the Literature: Implications for the Pathomechanism

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Subject Area:
Endocrinology , Women's and Children's Health
Stella A. Nagel, Michaela F. Hartmann, Felix G. Riepe, Stefan A. Wudy, Martin Wabitsch
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2019) 91 (5): 336–345.
https://doi.org/10.1159/000495189
Published Online: 11 December 2018
View articletitled, Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation – A Case Report and Review of the Literature: Implications for the Pathomechanism
Open the PDF for Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation – A Case Report and Review of the Literature: Implications for the Pathomechanism in another window
Journal Articles

17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene

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Subject Area:
Endocrinology , Women's and Children's Health
Christina Petri, Stefan A. Wudy, Felix G. Riepe, Paul-Martin Holterhus, Jens Siegel, Michaela F. Hartmann, Alexandra E. Kulle, Maik Welzel, Joachim Grötzinger, Ralf L. Schild, Sabine Heger
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2014) 81 (5): 350–355.
https://doi.org/10.1159/000357065
Published Online: 04 April 2014
View articletitled, 17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene
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Journal Articles

The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development

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Subject Area:
Endocrinology , Women's and Children's Health
Bilgin Yüksel, Alexandra E. Kulle, Fatih Gürbüz, Maik Welzel, Damla Kotan, Eda Mengen, Paul-Martin Holterhus, Ali Kemal Topaloğlu, Joachim Grötzinger, Felix G. Riepe
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2013) 80 (3): 163–169.
https://doi.org/10.1159/000354086
Published Online: 01 August 2013
View articletitled, The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development
Open the PDF for The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development in another window
Journal Articles

Implementation of a Liquid Chromatography Tandem Mass Spectrometry Assay for Eight Adrenal C-21 Steroids and Pediatric Reference Data

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Subject Area:
Endocrinology , Women's and Children's Health
Alexandra E. Kulle, Maik Welzel, Paul-Martin Holterhus, Felix G. Riepe
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2013) 79 (1): 22–31.
https://doi.org/10.1159/000346406
Published Online: 16 January 2013
View articletitled, Implementation of a Liquid Chromatography Tandem Mass Spectrometry Assay for Eight Adrenal C-21 Steroids and Pediatric Reference Data
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Journal Articles

Neonatal Screening: Identification of Children with 11β-Hydroxylase Deficiency by Second-Tier Testing

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Subject Area:
Endocrinology , Women's and Children's Health
Nils Janzen, Felix G. Riepe, Michael Peter, Stefanie Sander, Ulrike Steuerwald, Eckhard Korsch, Friedrich Krull, Hermann L. Müller, Sabine Heger, Christoph Brack, Johannes Sander
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2012) 77 (3): 195–199.
https://doi.org/10.1159/000337974
Published Online: 13 April 2012
View articletitled, Neonatal Screening: Identification of Children with 11β-Hydroxylase Deficiency by Second-Tier Testing
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Journal Articles

Multiplex Ligation-Dependent Probe Amplification Analysis of the NR0B1(DAX1) Locus Enables Explanation of Phenotypic Differences in Patients with X-Linked Congenital Adrenal Hypoplasia

Open Access
Subject Area:
Endocrinology , Women's and Children's Health
Michela Barbaro, Susanne Bens, Andrea Haake, Michael Peter, Jürgen Brämswig, Paul-Martin Holterhus, Juan Pedro Lopez-Siguero, Udo Menken, Monika Mix, Wolfgang G. Sippell, Anna Wedell, Felix G. Riepe
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2012) 77 (2): 100–107.
https://doi.org/10.1159/000336344
Published Online: 23 March 2012
View articletitled, Multiplex Ligation-Dependent Probe Amplification Analysis of the NR0B1(DAX1) Locus Enables Explanation of Phenotypic Differences in Patients with X-Linked Congenital Adrenal Hypoplasia
Open the PDF for Multiplex Ligation-Dependent Probe Amplification Analysis of the NR0B1(DAX1) Locus Enables Explanation of Phenotypic Differences in Patients with X-Linked Congenital Adrenal Hypoplasia in another window
Journal Articles

Serum Concentrations of Adrenal Steroids and Their Precursors as a Measure of Maturity of Adrenocortical Function in Very Premature Newborns

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Subject Area:
Endocrinology , Women's and Children's Health
Päivi Nykänen, Kirsti Heinonen, Felix G. Riepe, Wolfgang G. Sippell, Raimo Voutilainen
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2010) 74 (5): 358–364.
https://doi.org/10.1159/000314970
Published Online: 07 July 2010
View articletitled, Serum Concentrations of Adrenal Steroids and Their Precursors as a Measure of Maturity of Adrenocortical Function in Very Premature Newborns
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Journal Articles

Congenital Adrenal Hyperplasia due to 11-Hydroxylase Deficiency – Insights from Two Novel CYP11B1 Mutations (p.M92X, p.R453Q)

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Subject Area:
Endocrinology , Women's and Children's Health
Nils Krone, Joachim Grötzinger, Paul-Martin Holterhus, Wolfgang G. Sippell, Hans-Peter Schwarz, Felix G. Riepe
Journal: Hormone Research in Paediatrics
Hormone Research (2009) 72 (5): 281–286.
https://doi.org/10.1159/000245930
Published Online: 19 October 2009
View articletitled, Congenital Adrenal Hyperplasia due to 11-Hydroxylase Deficiency – Insights from Two Novel CYP11B1 Mutations (p.M92X, p.R453Q)
Open the PDF for Congenital Adrenal Hyperplasia due to 11-Hydroxylase Deficiency – Insights from Two Novel CYP11B1 Mutations (p.M92X, p.R453Q) in another window
Journal Articles

Clinical and Molecular Features of Type 1 Pseudohypoaldosteronism

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Subject Area:
Endocrinology , Women's and Children's Health
Felix G. Riepe
Journal: Hormone Research in Paediatrics
Hormone Research (2009) 72 (1): 1–9.
https://doi.org/10.1159/000224334
Published Online: 30 June 2009
View articletitled, Clinical and Molecular Features of Type 1 Pseudohypoaldosteronism
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Journal Articles

Long-Term Follow-Up of Spontaneous Development in a Boy with Familial Male Precocious Puberty

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Subject Area:
Endocrinology , Women's and Children's Health
Carl-Joachim Partsch, Nils Krone, Felix G. Riepe, Jörg Gromoll, Wolfgang G. Sippell
Journal: Hormone Research in Paediatrics
Hormone Research (2004) 62 (4): 177–181.
https://doi.org/10.1159/000080887
Published Online: 21 October 2004
View articletitled, Long-Term Follow-Up of Spontaneous Development in a Boy with Familial Male Precocious Puberty
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Journal Articles

Treatment of Pubertal Gynecomastia with the Specific Aromatase Inhibitor Anastrozole

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Subject Area:
Endocrinology , Women's and Children's Health
Felix G. Riepe, Inka Baus, Stephanie Wiest, Nils Krone, Wolfgang G. Sippell, Carl-Joachim Partsch
Journal: Hormone Research in Paediatrics
Hormone Research (2004) 62 (3): 113–118.
https://doi.org/10.1159/000079882
Published Online: 10 September 2004
View articletitled, Treatment of Pubertal Gynecomastia with the Specific Aromatase Inhibitor Anastrozole
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Journal Articles

Management of Congenital Adrenal Hyperplasia: Results of the ESPE Questionnaire

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Subject Area:
Endocrinology , Women's and Children's Health
Felix G. Riepe, Nils Krone, Matthias Viemann, Carl-Joachim Partsch, Wolfgang G. Sippell
Journal: Hormone Research in Paediatrics
Hormone Research (2002) 58 (4): 196–205.
https://doi.org/10.1159/000065492
Published Online: 19 September 2002
View articletitled, Management of Congenital Adrenal Hyperplasia: Results of the ESPE Questionnaire
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