Schulze, Andreas Prof. Dr. sc. med.Universität HeidelbergHeidelberg
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Co-author (Univ. of Heidelberg)
- Lindner, Martin (2)
- Pöschl, Johannes (1)
- Kölker, Stefan (1)
- Schlemmer, Heinz-Peter (1)
- Ebinger, Friedrich (1)
- Heß, Thomas (1)
- Knopp, Michael V. (1)
- Linderkamp, Otwin (1)
- Harting, Inga (1)
- Dunckelmann, Robert (1)
- Okun, Jürgen G. (1)
- Meyburg, Jochen (1)
- Trefz, Friedrich K. (1)
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Publications in heiBIB 
- Schulze, Andreas: Lack of creatine in muscle and brain in an adult with GAMT deficiency / Andreas Schulze, Peter Bachert, Heinz Schlemmer, Inga Harting, Tilman Polster, Gajja S. Salomons, Na… , 23 January 2003. - 4 S.
In: Annals of neurology, ISSN 1531-8249. 53(2003), 2, Seite 248-251
DOI: 10.1002/ana.10455
- Schulze, Andreas: Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry : results, outcome, and implications / Andreas Schulze, Martin Lindner, Dirk Kohlmüller, Katharina Olgemöller, Ertan Mayatepek, Georg F. Ho… , June 1, 2003. - 8 S.
In: Pediatrics, ISSN 1098-4275. 111(2003), 6, Seite 1399-1406
DOI: 10.1542/peds.111.6.1399
- Schulze, Andreas: Elektrospray Tandem-Massenspektrometrie : ein neues Vefahren für das Neugeborenen-Screening auf hereditäre Stoffwechselkrankheiten / vorgelegt von Andreas Schulze, 2003. - Getr. Zählung : Ill., graph. Darst.
- Schulze, Andreas: Evaluation of 6-year application of the enzymatic colorimetric phenylalanine assay in the setting of neonatal screening for phenylketonuria. In memoriam Horst Bickel. / Andreas Schulze, Ertan Mayatepek, Georg F. Hoffmann, 2002. - 11 S.
In: Clinica chimica acta, ISSN 1873-3492. 317(2002), 1, Seite 27-37
DOI: 10.1016/S0009-8981(01)00736-7
- Okun, Jürgen G.: A method for quantitative acylcarnitine profiling in human skin fibroblasts using unlabelled palmitic acid : diagnosis of fatty acid oxidation disorders and differentiation between biochemical phenotypes of MCAD deficiency / Jürgen G Okun, Stefan Kölker, Andreas Schulze, Dirk Kohlmüller, Katharina Olgemöller, Martin Lindner… , 19 September 2002. - 8 S.
In: Biochimica et biophysica acta, ISSN 1879-2618. 1584(2002), 2, Seite 91-98
DOI: 10.1016/S1388-1981(02)00296-2
- Meyburg, Jochen: Acylcarnitine profiles of preterm infants over the first four weeks of life / Jochen Meyburg, Andreas Schulze, Dirk Kohlmueller, Johannes Pöschl, Otwin Linderkamp, Georg F. Hoffm… , April 22, 2002. - 4 S.
In: Pediatric research, ISSN 1530-0447. 52(2002), 5, Seite 720-723
DOI: 10.1203/00006450-200211000-00018
- Dunckelmann, Robert: 2-ketoglutarate dehydrogenase deficiency with intermittent 2-ketoglutaric aciduria / R.J. Dunckelmann, F. Ebinger, A. Schulze, R.J.A. Wanders, D. Rating, E. Mayatepek, 31. Dezember 2000. - 4 S.
In: Neuropediatrics, ISSN 1439-1899. 31(2000), 01, Seite 35-38
DOI: 10.1055/s-2000-15295
- Schulze, Andreas: Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency : Diagnostic tools for a new inborn error of metabolism / Andreas Schulze, Thomas Hess, Ron Wevers, Ertan Mayatepek, Peter Bachert, Bart Marescau, Michael V. … , October 1997. - 6 S.
In: The journal of pediatrics, ISSN 1097-6833. 131(1997), 4, Seite 626-631
DOI: 10.1016/S0022-3476(97)70075-1
- Schulze, Andreas: Sakaguchi reaction : a useful method for screening guanidinoacetate-methyltransferase deficiency / A. Schulze, E. Mayatepek, D. Rating, H.J. Bremer, 01 September 1996. - 1 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 19(1996), 5, Seite 706
DOI: 10.1007/BF01799854
- Mayatepek, Ertan: Atypical vitamin B12-unresponsive methylmalonic aciduria in a sibship with severe progressive encephalomyelopathy : a new genetic disease? / E. Mayatepek, G.F. Hoffmann, R. Baumgartner, A. Schulze, C. Jakobs, F.K. Trefz, H.J. Bremer, May 1996. - 6 S.
In: European journal of pediatrics, ISSN 1432-1076. 155(1996), 5, Seite 398-403
DOI: 10.1007/BF01955272
