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Egbert Schulze
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Journal Articles

Clinical Features and Response to Treatment of Prolactinomas in Children and Adolescents: A Retrospective Single-Centre Analysis and Review of the Literature

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Subject Area:
Endocrinology , Women's and Children's Health
Thomas Breil, Catherine Lorz, Daniela Choukair, Janna Mittnacht, Ioana Inta, Daniela Klose, Jessica Jesser, Egbert Schulze, Markus Bettendorf
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2018) 89 (3): 157–165.
https://doi.org/10.1159/000486280
Published Online: 16 February 2018
View articletitled, Clinical Features and Response to Treatment of Prolactinomas in Children and Adolescents: A Retrospective Single-Centre Analysis and Review of the Literature
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Journal Articles

Diagnosis of Glucocorticoid-Remediable Aldosteronism in Hypertensive Children

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Subject Area:
Endocrinology , Women's and Children's Health
Clemens Kamrath, Christiane Maser-Gluth, Christine Haag, Egbert Schulze
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2011) 76 (2): 93–98.
https://doi.org/10.1159/000326524
Published Online: 27 May 2011
View articletitled, Diagnosis of Glucocorticoid-Remediable Aldosteronism in Hypertensive Children
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Journal Articles

Alterations in Lipid and Carbohydrate Metabolism in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

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Subject Area:
Endocrinology , Women's and Children's Health
Anca Zimmermann, Paula Grigorescu-Sido, Camelia AlKhzouz, Karen Patberg, Simona Bucerzan, Egbert Schulze, Tim Zimmermann, Heidi Rossmann, Hans-Christian Geiss, Karl J. Lackner, Matthias M. Weber
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2010) 74 (1): 41–49.
https://doi.org/10.1159/000313368
Published Online: 15 April 2010
View articletitled, Alterations in Lipid and Carbohydrate Metabolism in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
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Journal Articles

A Homozygous L299P Mutation in the CYP11B1 Gene Leads to Complete Virilization in 46,XX Individuals with 11-Beta-Hydroxylase Deficiency

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Subject Area:
Endocrinology , Women's and Children's Health
Stefan Riedl, Huy-Hoang Nguyen, Susanne Clausmeyer, Egbert Schulze, Franz Waldhauser, Rita Bernhardt
Journal: Hormone Research in Paediatrics
Hormone Research (2008) 70 (3): 145–149.
https://doi.org/10.1159/000137659
Published Online: 29 July 2008
View articletitled, A Homozygous L299P Mutation in the CYP11B1 Gene Leads to Complete Virilization in 46,XX Individuals with 11-Beta-Hydroxylase Deficiency
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Journal Articles

Screening for Pax8 Mutations in Patients with Congenital Hypothyroidism in South-West Germany

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Subject Area:
Endocrinology , Women's and Children's Health
Kirsten Lanzerath, Markus Bettendorf, Christine Haag, Caroline Kneppo, Egbert Schulze, Jürgen Grulich-Henn
Journal: Hormone Research in Paediatrics
Hormone Research (2006) 66 (2): 96–100.
https://doi.org/10.1159/000093799
Published Online: 26 July 2006
View articletitled, Screening for Pax8 Mutations in Patients with Congenital Hypothyroidism in South-West Germany
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Journal Articles

Growth Analysis in Patients with 21-Hydroxylase Deficiency Influence of Glucocorticoid Dosage, Age at Diagnosis, Phenotype and Genotype on Growth and Height Outcome

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Subject Area:
Endocrinology , Women's and Children's Health
Anca Grigorescu-Sido, Markus Bettendorf, Egbert Schulze, Ileana Duncea, Udo Heinrich
Journal: Hormone Research in Paediatrics
Hormone Research (2003) 60 (2): 84–90.
https://doi.org/10.1159/000071876
Published Online: 31 July 2003
View articletitled, Growth Analysis in Patients with 21-Hydroxylase Deficiency Influence of Glucocorticoid Dosage, Age at Diagnosis, Phenotype and Genotype on Growth and Height Outcome
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