H. Hammen

发表

Analysis of concentration and (13)C enrichment of D-galactose in human plasma.

U. Wendel, K. Loganathan, P. Schadewaldt, 2000, Clinical chemistry.

Endogenous galactose formation in galactose-1-phosphate uridyltransferase deficiency

J. Kotzka, U. Wendel, P. Schadewaldt, 2014, Archives of physiology and biochemistry.

Age dependence of endogenous galactose formation in Q188R homozygous galactosemic patients.

U. Wendel, P. Schadewaldt, H. Hammen, 2004, Molecular genetics and metabolism.

Assessment of Whole Body L-Leucine Oxidation by Noninvasive L-[1-13C]Leucine Breath Tests: A Reappraisal in Patients with Maple Syrup Urine Disease, Obligate Heterozygotes, and Healthy Subjects1

U. Wendel, P. Schadewaldt, H. Hammen, 1998, Pediatric Research.

Renal excretion of galactose and galactitol in patients with classical galactosaemia, obligate heterozygous parents and healthy subjects

K. Strassburger, U. Wendel, P. Schadewaldt, 2003, Journal of Inherited Metabolic Disease.

Renal clearance of branched-chain L-amino and 2-oxo acids in maple syrup urine disease

U. Wendel, A. Ott, P. Schadewaldt, 1999, Journal of Inherited Metabolic Disease.

Whole Body Branched-Chain L-Amino Acid Oxidation in Overnight Fasted Human Subjects

W. Renn, U. Wendel, P. Schadewaldt, 1997 .

Enzymatic-chemical preparation of quinoxaline derivatives from L-amino acids for gas chromatographic-mass spectrometric analyses.

U. Wendel, U. Matthiesen, P. Schadewaldt, 1995, Analytical biochemistry.

Significance of L-alloisoleucine in plasma for diagnosis of maple syrup urine disease.

U. Wendel, P. Schadewaldt, H. Hammen, 1999, Clinical chemistry.

Transamination and oxidative decarboxylation of L-isoleucine, L-alloisoleucine and related 2-oxo acids in perfused rat hind limb muscle.

W. Radeck, W. Staib, P. Schadewaldt, 1989, Biochimica et biophysica acta.

Human branched-chain L-amino acid aminotransferase: Activity and subcellular localization in cultured skin fibroblasts

U. Wendel, P. Schadewaldt, H. Hammen, 1995, Amino Acids.

Urinary Excretion of Pentose Phosphate Pathway-Associated Polyols in Early Postnatal Life

A. Koy, E. Mayatepek, U. Wendel, 2008, Neonatology.

Stable-isotope dilution analysis of galactose metabolites in human erythrocytes.

U. Wendel, P. Schadewaldt, H. Hammen, 2003, Rapid communications in mass spectrometry : RCM.

On the mechanism ofl-alloisoleucine formation: Studies on a healthy subject and in fibroblasts from normals and patients with maple syrup urine disease

U. Wendel, P. Schadewaldt, H. Hammen, 1990, Journal of Inherited Metabolic Disease.

Galactonate determination in urine by stable isotope dilution gas chromatography-mass spectrometry.

U. Wendel, P. Schadewaldt, H. Hammen, 2004, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Whole-Body l-Leucine Oxidation in Patients with Variant Form of Maple Syrup Urine Disease

U. Wendel, P. Schadewaldt, H. Hammen, 2001, Pediatric Research.

Longitudinal Assessment of Intellectual Achievement in Patients With Classical Galactosemia

U. Wendel, B. Hoffmann, S. Schweitzer-Krantz, 2010, Pediatrics.

The cladocera of a ditch at Tienhoven

H. Hammen, E. Notenboom-Ram, B. Korf, 1976, Hydrobiological Bulletin.

Formation of L-Alloisoleucine In Vivo : An L-[13C]Isoleucine Study in Man

U. Wendel, P. Schadewaldt, H. Hammen, 2000, Pediatric Research.

Determination of R- and S-3-methyl-2-oxopentanoate enantiomers in human plasma: suitable method for label enrichment analysis.

U. Wendel, P. Schadewaldt, H. Hammen, 1996, Journal of chromatography. B, Biomedical applications.

Transamination and Oxidative Decarboxylation Rates of Branched-Chain 2-Oxo Acids in Cultured Human Skin Fibroblasts

U. Wendel, W. Radeck, P. Schadewaldt, 1988, Pediatric Research.

Biochemical monitoring of pregnancy and breast feeding in five patients with classical galactosaemia – and review of the literature

G. Boers, M. Janssen, A. Bosch, 2009, European Journal of Pediatrics.