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Michael Peter
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Journal Articles

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

Available to Purchase
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

Congenital Hyperreninemic Hypoaldosteronism:Are There Different Forms?: Commentary to E. Leshinsky-Silver et al.: Congenital Hyperreninemic Hypoaldosteronismin Israel: Sequence Analysis of CYP11B2 Gene (Horm Res 2006;66:73–78)

Available to Purchase
Subject Area:
Endocrinology , Women's and Children's Health
Michael Peter
Journal: Hormone Research in Paediatrics
Hormone Research (2006) 66 (2): 79–80.
https://doi.org/10.1159/000093584
Published Online: 26 July 2006
View articletitled, Congenital Hyperreninemic Hypoaldosteronism:Are There Different Forms?: Commentary to E. Leshinsky-Silver et al.: Congenital Hyperreninemic Hypoaldosteronismin Israel: Sequence Analysis of CYP11B2 Gene (Horm Res 2006;66:73–78)
Open the PDF for Congenital Hyperreninemic Hypoaldosteronism:Are There Different Forms?: Commentary to E. Leshinsky-Silver et al.: Congenital Hyperreninemic Hypoaldosteronismin Israel: Sequence Analysis of CYP11B2 Gene (Horm Res 2006;66:73–78) in another window
Journal Articles

Aldosterone Synthase Deficiency Type I: Hormonal and Genetic Analyses of Two Cases

Available to Purchase
Subject Area:
Endocrinology , Women's and Children's Health
Juan P. López-Siguero, Emilio García-García, Michael Peter, Wolfgang G. Sippell
Journal: Hormone Research in Paediatrics
Hormone Research (1999) 52 (6): 298–300.
https://doi.org/10.1159/000023500
Published Online: 13 July 2000
View articletitled, Aldosterone Synthase Deficiency Type I: Hormonal and Genetic Analyses of Two Cases
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