Steuerwald U - Search Results

1

2-Methylbutyryl-coenzyme A dehydrogenase deficiency: functional and molecular studies on a defect in isoleucine catabolism.

Sass JO, Ensenauer R, Röschinger W, Reich H, Steuerwald U, Schirrmacher O, Engel K, Häberle J, Andresen BS, Mégarbané A, Lehnert W, Zschocke J. Sass JO, et al. Among authors: steuerwald u. Mol Genet Metab. 2008 Jan;93(1):30-5. doi: 10.1016/j.ymgme.2007.09.002. Epub 2007 Oct 22. Mol Genet Metab. 2008. PMID: 17945527

2

Neonatal screening for citrullinaemia.

Sander J, Janzen N, Sander S, Steuerwald U, Das AM, Scholl S, Trefz FK, Koch HG, Häberle J, Korall H, Marquardt I, Korenke C. Sander J, et al. Among authors: steuerwald u. Eur J Pediatr. 2003 Jun;162(6):417-20. doi: 10.1007/s00431-003-1177-z. Epub 2003 Apr 8. Eur J Pediatr. 2003. PMID: 12684898

3

Neonatal screening for defects of the mitochondrial trifunctional protein.

Sander J, Sander S, Steuerwald U, Janzen N, Peter M, Wanders RJ, Marquardt I, Korenke GC, Das AM. Sander J, et al. Among authors: steuerwald u. Mol Genet Metab. 2005 Jun;85(2):108-14. doi: 10.1016/j.ymgme.2005.02.002. Epub 2005 Mar 24. Mol Genet Metab. 2005. PMID: 15896654

4

UPLC-MS/MS analysis of C5-acylcarnitines in dried blood spots.

Janzen N, Steuerwald U, Sander S, Terhardt M, Peter M, Sander J. Janzen N, et al. Among authors: steuerwald u. Clin Chim Acta. 2013 Jun 5;421:41-5. doi: 10.1016/j.cca.2013.03.001. Epub 2013 Mar 13. Clin Chim Acta. 2013. PMID: 23499962

5

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 FK, Das AM. Sander J, et al. Among authors: steuerwald u. Clin Chem. 2006 Mar;52(3):482-7. doi: 10.1373/clinchem.2005.059790. Epub 2006 Jan 26. Clin Chem. 2006. PMID: 16439608

6

EDTA in dried blood spots leads to false results in neonatal endocrinologic screening.

Holtkamp U, Klein J, Sander J, Peter M, Janzen N, Steuerwald U, Blankenstein O. Holtkamp U, et al. Among authors: steuerwald u. Clin Chem. 2008 Mar;54(3):602-5. doi: 10.1373/clinchem.2007.096685. Clin Chem. 2008. PMID: 18310148

7

Neonatal screening for medium chain acyl-CoA deficiency: high incidence in Lower Saxony (northern Germany).

Sander S, Janzen N, Janetzky B, Scholl S, Steuerwald U, Schäfer J, Sander J. Sander S, et al. Among authors: steuerwald u. Eur J Pediatr. 2001 May;160(5):318-9. doi: 10.1007/pl00008439. Eur J Pediatr. 2001. PMID: 11388605 No abstract available.

8

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. Janzen N, et al. Among authors: steuerwald u. J Clin Endocrinol Metab. 2007 Jul;92(7):2581-9. doi: 10.1210/jc.2006-2890. Epub 2007 Apr 24. J Clin Endocrinol Metab. 2007. PMID: 17456574 Clinical Trial.

9

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 AM, Sander J. Janzen N, et al. Among authors: steuerwald u. Steroids. 2011 Dec 11;76(13):1437-42. doi: 10.1016/j.steroids.2011.07.013. Epub 2011 Aug 2. Steroids. 2011. PMID: 21839763

10

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

Janzen N, Riepe FG, Peter M, Sander S, Steuerwald U, Korsch E, Krull F, Müller HL, Heger S, Brack C, Sander J. Janzen N, et al. Among authors: steuerwald u. Horm Res Paediatr. 2012;77(3):195-9. doi: 10.1159/000337974. Epub 2012 Apr 13. Horm Res Paediatr. 2012. PMID: 22508345

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