Works by Sander, Stefanie

Results: 8

Neonatal Screening: Identification of Children with 11β-Hydroxylase Deficiency by Second-Tier Testing.

Published in:

Hormone Research in Paediatrics, 2012, v. 77, n. 3, p. 195, doi. 10.1159/000337974

By:

Janzen, Nils;
Riepe, Felix G.;
Peter, Michael;
Sander, Stefanie;
Steuerwald, Ulrike;
Korsch, Eckhard;
Krull, Friedrich;
Müller, Hermann L.;
Heger, Sabine;
Brack, Christoph;
Sander, Johannes

Publication type:

Article

Neonatal screening for citrullinaemia.

Published in:

2003

By:

Sander, Johannes;
Janzen, Nils;
Sander, Stefanie;
Steuerwald, Ulrike;
Das, Anibh M.;
Scholl, Sabine;
K.Trefz, Friedrich;
Koch, Hans-Georg;
Häberle, Johannes;
Korall, Herbert;
Marquardt, Iris;
Korenke, Christoph;
Trefz, Friedrich K

Publication type:

journal article

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

Published in:

2001

By:

Sander, Stefanie;
Janzen, Nils;
Janetzky, Bernd;
Scholl, Sabine;
Steuerwald, Ulrike;
Schäfer, Jochen;
Sander, Johannes;
Sander, S;
Janzen, N;
Janetzky, B;
Scholl, S;
Steuerwald, U;
Schäfer, J;
Sander, J

Publication type:

Letter

Detection of MCPG metabolites in horses with atypical myopathy.

Published in:

PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0211698

By:

Bochnia, Mandy;
Sander, Johannes;
Ziegler, Joerg;
Terhardt, Michael;
Sander, Stefanie;
Janzen, Nils;
Cavalleri, Jessika-M. V.;
Zuraw, Aleksandra;
Wensch-Dorendorf, Monika;
Zeyner, Annette

Publication type:

Article

Energy metabolism in umbilical endothelial cells from preterm and term neonates.

Published in:

Journal of Perinatal Medicine, 2011, v. 39, n. 5, p. 587, doi. 10.1515/JPM.2011.063

By:

Illsinger, Sabine;
Janzen, Nils;
Sander, Stefanie;
Bode, Julia;
Mallunat, Lisa;
Thomasmeyer, Rena;
Hagebölling, Friederike;
Schmidt, Karl-Heinz;
Bednarczyk, Jolanthe;
Vaske, Bernhard;
Lücke, Thomas;
Das, Anibh M.

Publication type:

Article

Rapid diagnosis of hypoglycin A intoxication in atypical myopathy of horses.

Published in:

Journal of Veterinary Diagnostic Investigation, 2016, v. 28, n. 2, p. 98, doi. 10.1177/1040638715624736

By:

Sander, Johannes;
Cavalleri, Jessika-M. V.;
Terhardt, Michael;
Bochnia, Mandy;
Zeyner, Annette;
Zuraw, Aleksandra;
Sander, Stefanie;
Peter, Michael;
Janzen, Nils

Publication type:

Article

Preeclampsia and HELLP Syndrome: Impaired Mitochondrial Function in Umbilical Endothelial Cells.

Published in:

Reproductive Sciences, 2010, v. 17, n. 3, p. 219, doi. 10.1177/1933719109351597

By:

Illsinger, Sabine;
Janzen, Nils;
Sander, Stefanie;
Schmidt, Karl-Heinz;
Bednarczyk, Jolanthe;
Mallunat, Lisa;
Bode, Julia;
Hagebölling, Friederike;
Hoy, Ludwig;
Lücke, Thomas;
Hass, Ralf;
Das, Anibh M.

Publication type:

Article

Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1).

Published in:

1998

By:

Sander, Stefanie;
Nicholson, Garth A.;
Ouvrier, Robert A.;
McLeod, James G.;
Pollard, John D.;
Sander, S;
Nicholson, G A;
Ouvrier, R A;
McLeod, J G;
Pollard, J D

Publication type:

journal article