Riepe, Felix G.

Homozygous disruption of P450 side-chain cleavage (CYP11A1) is associated with prematurity, complete 46,XY sex reversal, and severe adrenal failure

Hiort, O., Holterhus, P.-M., Werner, R., Marschke, C., Hoppe, U., Partsch, C.-J., Riepe, F. G., Achermann, J. C., & Struve, D. (2005) · The Journal of Clinical Endocrinology & Metabolism

Adrenal Hormones and DisordersSexual Differentiation and Disorders

Cited by 120

Blood Pressure in a Large Cohort of Children and Adolescents With Classic Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency

Bonfig, W., Roehl, F.-W., Riedl, S., Dörr, H. G., Bettendorf, M., Brämswig, J., Schönau, E., Riepe, F., Hauffa, B., Holl, R. W., et al. (2016) · American Journal of Hypertension

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 84

Management of Congenital Adrenal Hyperplasia: Results of the ESPE Questionnaire

Riepe, F. G., Krone, N., Viemann, M., Partsch, C.-J., & Sippell, W. G. (2002) · Hormone Research in Paediatrics

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 72

Genotype/phenotype correlations in 538 congenital adrenal hyperplasia patients from Germany and Austria: discordances in milder genotypes and in screened versus prescreening patients

Riedl, S., Röhl, F.-W., Bonfig, W., Brämswig, J., Richter-Unruh, A., Fricke-Otto, S., Bettendorf, M., Riepe, F., Kriegshäuser, G., Schönau, E., et al. (2019) · Endocrine Connections

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 69

Neonatal screening: identification of children with 11β-hydroxylase deficiency by second-tier testing

Janzen, N., Riepe, F. G., Peter, M., Sander, S., Steuerwald, U., Korsch, E., Krull, F., Müller, H. L., Heger, S., Brack, C., et al. (2012) · Hormone Research in Paediatrics

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 37

Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia: identification, functional characterization, and structural analysis

Grischuk, Y., Rubtsov, P., Riepe, F. G., Grötzinger, J., Beljelarskaia, S., Prassolov, V., Kalintchenko, N., Semitcheva, T., Peterkova, V., Tiulpakov, A., et al. (2006) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 33

Testosterone synthesis in patients with 17β-hydroxysteroid dehydrogenase 3 deficiency

Werner, R., Kulle, A., Sommerfeld, I., Riepe, F. G., Wudy, S., Hartmann, M. F., Merz, H., Döhnert, U., Bertelloni, S., Holterhus, P.-M., et al. (2012) · Sexual Development

Sexual Differentiation and DisordersGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 29

Absence of exercise-induced leptin suppression associated with insufficient epinephrine reserve in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Riepe, F., Krone, N., Krüger, S., Sweep, F., Lenders, J., Dötsch, J., Mönig, H., Sippell, W., & Partsch, C.-J. (2006) · Experimental and Clinical Endocrinology & Diabetes

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 27

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

Krone, N., Grötzinger, J., Holterhus, P.-M., Sippell, W. G., Schwarz, H.-P., & Riepe, F. G. (2009) · Hormone Research in Paediatrics

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 24

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms

Ben Charfeddine, I., Riepe, F. G., Clauser, E., Ayedi, A., Makni, S., Sfar, M. T., Sboui, H., Kahloul, N., Ben Hamouda, H., Chouchane, S., et al. (2012) · Gene

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 19

Functional characterization of three CYP21A2 sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co-expression system: Functional Characterization of CYP21A2 Variants

Bleicken, C., Loidi, L., Dhir, V., Parajes, S., Quinteiro, C., Dominguez, F., Grötzinger, J., Sippell, W. G., Riepe, F. G., Arlt, W., et al. (2009) · Human Mutation

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 15