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Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 1, 1994
Oxygen free radicals and antioxidants in cystic fibrosis: the concept of an oxidant-antioxidant imbalanceB M Winklhofer-Roob
Current Opinion in Clinical Nutrition and Metabolic Care|August 10, 2000
Cystic fibrosis: nutritional status and micronutrientsB M Winklhofer-Roob
European Journal of Pediatrics|August 1, 1991
Human leucocyte class I and II antigens in coeliac disease: a study in an Austrian paediatric populationB M Winklhofer-Roob, E Rossipal, G Lanzer
Journal of Lipid Research|February 11, 1998
RRR-alpha-tocopherol can be substituted for by Trolox in determination of kinetic parameters of LDL oxidizability by copperA R Bergmann, P Ramos, H Esterbauer, et al.
Clinical Chemistry|January 1, 1997
Reference values for plasma concentrations of vitamin E and A and carotenoids in a Swiss population from infancy to adulthood, adjusted for seasonal influencesB M Winklhofer-Roob, M A van't Hof, D H Shmerling
Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1992
Progressive idiopathic cholestasis presenting with profuse watery diarrhoea and recurrent infections (Byler's disease)B M Winklhofer-Roob, D H Shmerling, R Solèr, et al.
The American Journal of Clinical Nutrition|May 1, 1996
Long-term oral vitamin E supplementation in cystic fibrosis patients: RRR-alpha-tocopherol compared with all-rac-alpha-tocopheryl acetate preparationsB M Winklhofer-Roob, M A van't Hof, D H Shmerling
Acta Paediatrica (Oslo, Norway : 1992)|October 1, 1995
Response to oral beta-carotene supplementation in patients with cystic fibrosis: a 16-month follow-up studyB M Winklhofer-Roob, M A van't Hof, D H Shmerling
The American Journal of Clinical Nutrition|May 1, 1996
Response to a single oral dose of all-rac-alpha-tocopheryl acetate in patients with cystic fibrosis and in healthy individualsB M Winklhofer-Roob, P E Tuchschmid, L Molinari, et al.
The American Journal of Clinical Nutrition|January 1, 1992
Short-term changes in erythrocyte alpha-tocopherol content of vitamin E-deficient patients with cystic fibrosisB M Winklhofer-Roob, D H Shmerling, M G Schimek, et al.
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