Peter, Michael

Newborn screening for congenital adrenal hyperplasia: additional steroid profile using liquid chromatography-tandem mass spectrometry

Janzen, N., Peter, M., Sander, S., Steuerwald, U., Terhardt, M., Holtkamp, U., & Sander, J. (2007) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 211

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

Rapid steroid hormone quantification for congenital adrenal hyperplasia (CAH) in dried blood spots using UPLC liquid chromatography-tandem mass spectrometry

Janzen, N., Sander, S., Terhardt, M., Steuerwald, U., Peter, M., Das, A. M., & Sander, J. (2011) · Steroids

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 66

Newborn Screening for Hepatorenal Tyrosinemia: Tandem Mass Spectrometric Quantification of Succinylacetone

Sander, J., Janzen, N., Peter, M., Sander, S., Steuerwald, U., Holtkamp, U., Schwahn, B., Mayatepek, E., Trefz, F. K., & Das, A. M. (2006) · Clinical Chemistry

Metabolism and Genetic DisordersNeonatal Health and Biochemistry

Cited by 62

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

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

Monitoring tyrosinaemia type I: Blood spot test for nitisinone (NTBC)

Sander, J., Janzen, N., Terhardt, M., Sander, S., Gökcay, G., Demirkol, M., Ozer, I., Peter, M., & Das, A. M. (2011) · Clinica Chimica Acta

Metabolism and Genetic DisordersAnalytical Methods in Pharmaceuticals

Cited by 32

Therapy monitoring in congenital adrenal hyperplasia by dried blood samples

Wieacker, I., Peter, M., Borucki, K., Empting, S., Roehl, F.-W., & Mohnike, K. (2015) · Journal of Pediatric Endocrinology and Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 14