Sippell, Wolfgang G.

Infusion of low dose etomidate: correction of hypercortisolemia in patients with Cushing's syndrome and dose-response relationship in normal subjects

SCHULTE, H. M., BENKER, G., REINWEIN, D., SIPPELL, W. G., & ALLOLIO, B. (1990) · The Journal of Clinical Endocrinology & Metabolism

Adrenal Hormones and DisordersPituitary Gland Disorders and Treatments

Cited by 156

New Insight into the Molecular Basis of 3β-Hydroxysteroid Dehydrogenase Deficiency: Identification of Eight Mutations in the HSD3B2 Gene in Eleven Patients from Seven New Families and Comparison of the Functional Properties of Twenty-Five Mutant Enzymes1

Moisan, A. M., Ricketts, M. L., Tardy, V., Desrochers, M., Mébarki, F., Chaussain, J.-L., Cabrol, S., Raux-Demay, M. C., Forest, M. G., Sippell, W. G., et al. (1999) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 107

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

The steroid hormonal milieu of the undisturbed human fetus and mother at 16–20 weeks gestation

PARTSCH, C.-J., SIPPELL, W. G., MACKENZIE, I. Z., & AYNSLEY-GREEN, A. (1991) · The Journal of Clinical Endocrinology & Metabolism

Adrenal Hormones and DisordersBirth, Development, and Health

Cited by 52

Amino acid substitution R384P in aldosterone synthase causes corticosterone methyloxidase type I deficiency

Geley, S., Jöhrer, K., Peter, M., Denner, K., Bernhardt, R., Sippell, W. G., & Kofler, R. (1995) · The Journal of Clinical Endocrinology & Metabolism

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 48

Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination

Peter, M., Sippell, W. G., Lorenzen, F., Westphal, E., Willig, R. P., & Grosse-Wilde, H. (1990) · The Lancet

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 41

Hereditary Defect in Biosynthesis of Aldosterone: Aldosterone Synthase Deficiency 1964–19971

Peter, M., Fawaz, L., Drop, S. L. S., Visser, H. K. A., & Sippell, W. G. (1997) · The Journal of Clinical Endocrinology & Metabolism

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 40

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

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

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