Publications by authors named "Udo Wendel"

46Publications

Endogenous galactose formation in galactose-1-phosphate uridyltransferase deficiency.

Arch Physiol Biochem 2014 Dec 30;120(5):228-39. Epub 2014 Sep 30.

Institute of Clinical Biochemistry and Pathobiochemistry, German Diabetes Center at the Heinrich-Heine-University Duesseldorf, Leibniz Center for Diabetes Research , Duesseldorf , Germany and.

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December 2014

Clinical and neurocognitive outcome in symptomatic isovaleric acidemia.

Orphanet J Rare Dis 2012 Jan 25;7. Epub 2012 Jan 25.

Center for Pediatrics and Adolescent Medicine, Albert-Ludwigs-Universität Freiburg, Germany.

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January 2012

Cross-sectional analysis of speech and cognitive performance in 32 patients with classic galactosemia.

J Inherit Metab Dis 2011 Apr 24;34(2):421-7. Epub 2011 Feb 24.

Department of General Pediatrics, University Children's Hospital, Heinrich-Heine-University Düsseldorf, Siegen, Germany.

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April 2011

Longitudinal assessment of intellectual achievement in patients with classical galactosemia.

Pediatrics 2010 Feb 25;125(2):e374-81. Epub 2010 Jan 25.

Deutsches Diabetes Zentrum, Abteilung Klinische Biochemie und Pathobiochemie, Auf'm Hennekamp 65, D-40225 Düsseldorf, Germany.

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February 2010

Biochemical and genetic analysis of 3-methylglutaconic aciduria type IV: a diagnostic strategy.

Brain 2009 Jan 16;132(Pt 1):136-46. Epub 2008 Nov 16.

Department of Paediatrics, Nijmegen Center for Mitochondrial Disorders, Radbound University Medical Center Nijmegen, The Netherlands.

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January 2009

Urinary excretion of pentose phosphate pathway-associated polyols in early postnatal life.

Neonatology 2009 5;95(3):256-61. Epub 2008 Nov 5.

Department of General Pediatrics, University Children's Hospital, Düsseldorf, Germany.

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May 2009

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

Eur J Pediatr 2009 Jun 24;168(6):721-9. Epub 2008 Sep 24.

German Diabetic Centre, Department of Clinical Biochemistry and Pathobiochemistry, UKD, University of Düsseldorf, Düsseldorf, Germany.

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June 2009

Outcome and long-term follow-up of 36 patients with tetrahydrobiopterin deficiency.

Mol Genet Metab 2008 Mar 3;93(3):295-305. Epub 2007 Dec 3.

Division of Clinical Chemistry and Biochemistry, University Children's Hospital, Steinwiesstrasse 75, CH-8032 Zürich, Switzerland.

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March 2008

Cystic renal dysplasia as a leading sign of inherited metabolic disease.

Pediatr Nephrol 2007 Dec 19;22(12):2119-24. Epub 2007 Jul 19.

Department of General Pediatrics, University Children's Hospital, Heinrich-Heine-University, Moorenstrasse 5, 40225, Düsseldorf, Germany.

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December 2007