Udo Wendel

A familial progressive neurodegenerative disease with 2-oxoglutaric aciduria

U. Langenbeck, G. Hoffmann, P. Heidemann, 1982, European Journal of Pediatrics.

Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism

B. Hamel, U. Wendel, W. Ruitenbeek, 1996, Journal of Inherited Metabolic Disease.

Maple syrup urine disease: Mutation analysis in Turkish patients

T. Coşkun, M. Henneke, K. Özgül, 2002, Journal of Inherited Metabolic Disease.

Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle

H. T. ter Laak, H. Laak, U. Wendel, 1996, Neurology.