Sander, Stefanie
5 papers on CoChat
Most cited papers
- Verified
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
- Verified
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
- Verified
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
- Verified
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
- Verified
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
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