Hartmann, Michaela F.

Increased activation of the alternative “backdoor” pathway in patients with 21-hydroxylase deficiency: evidence from urinary steroid hormone analysis

Kamrath, C., Hochberg, Z., Hartmann, M. F., Remer, T., & Wudy, S. A. (2012) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 191

Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency

Krone, N., Reisch, N., Idkowiak, J., Dhir, V., Ivison, H. E., Hughes, B. A., Rose, I. T., O'Neil, D. M., Vijzelaar, R., Smith, M. J., et al. (2012) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 163

Steroid hormone analysis in diagnosis and treatment of DSD: Position paper of Eu COST Action BM 1303 “DSDnet”

Kulle, A., Krone, N., Holterhus, P. M., Schuler, G., Greaves, R. F., Juul, A., de Rijke, Y. B., Hartmann, M. F., Saba, A., Hiort, O., et al. (2017) · European Journal of Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 111

Androgen excess is due to elevated 11-oxygenated androgens in treated children with congenital adrenal hyperplasia

Kamrath, C., Wettstaedt, L., Boettcher, C., Hartmann, M. F., & Wudy, S. A. (2018) · The Journal of Steroid Biochemistry and Molecular Biology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 71

Diagnosis of 21-hydroxylase deficiency by urinary metabolite ratios using gas chromatography–mass spectrometry analysis: reference values for neonates and infants

Kamrath, C., Hartmann, M. F., Boettcher, C., Zimmer, K.-P., & Wudy, S. A. (2016) · The Journal of Steroid Biochemistry and Molecular Biology

Sexual Differentiation and DisordersMetabolism and Genetic Disorders

Cited by 34

The Urinary Steroidome of Treated Children With Classic 21-Hydroxylase Deficiency

Kamrath, C., Wettstaedt, L., Boettcher, C., Hartmann, M. F., & Wudy, S. A. (2017) · The Journal of Steroid Biochemistry and Molecular Biology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 30

Urinary GC-MS steroid metabotyping in treated children with congenital adrenal hyperplasia

Kamrath, C., Hartmann, M. F., Pons-Kühnemann, J., & Wudy, S. A. (2020) · Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 28

Phenotypic, metabolic, and molecular genetic characterization of six patients with congenital adrenal hyperplasia caused by novel mutations in the CYP11B1 gene

Nguyen, H.-H., Eiden-Plach, A., Hannemann, F., Malunowicz, E. M., Hartmann, M. F., Wudy, S. A., & Bernhardt, R. (2016) · The Journal of Steroid Biochemistry and Molecular Biology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 21

Height Velocity Defined Metabolic Control in Children With Congenital Adrenal Hyperplasia Using Urinary Steroid GC-MS Analysis

Kamrath, C., Wettstaedt, L., Hartmann, M. F., & Wudy, S. A. (2019) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 18

Late diagnosis of 3β-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the HSD3B2 gene

Fanis, P., Neocleous, V., Kosta, K., Karipiadou, A., Hartmann, M. F., Wudy, S. A., Karantaglis, N., Papadimitriou, D. T., Skordis, N., Tsikopoulos, G., et al. (2021) · Journal of Pediatric Endocrinology and Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 10

A steroid metabolomic approach to 17α-hydroxylase/17,20 lyase deficiency

Tiosano, D., Navon, R., Flor, O., Knopf, C., Hartmann, M. F., Wudy, S. A., Yakhini, Z., & Hochberg, Z. (2010) · Metabolomics

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 4