Bibliotecas PUC-SP - Busca Integrada

Cefuroxime plasma and CSF levels in children with meningitis.

de réir Corbeel, L, Van Acker, G, Eeckels, R, Vandepitte, J, Verbist, L
Foilsithe / Cruthaithe 1979

Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.

de réir Corbeel, L. M., Colombo, J. P., Van Sande, M., Weber, A.
Foilsithe / Cruthaithe 1969

Ultrastructural abnormalities of bronchial cilia in children with recurrent airway infections and bronchiectasis.

de réir Corbeel, L, Cornillie, F, Lauweryns, J, Boel, M, van den Berghe, G
Foilsithe / Cruthaithe 1981

Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).

de réir de Boer, M, de Klein, A, Hossle, J P, Seger, R, Corbeel, L, Weening, R S, Roos, D
Foilsithe / Cruthaithe 1992

Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridization.

de réir Weening, R S, Corbeel, L, de Boer, M, Lutter, R, van Zwieten, R, Hamers, M N, Roos, D
Foilsithe / Cruthaithe 1985

Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspects.

de réir Corbeel, L, Tada, K, Colombo, J P, Eeckels, R, Eggermont, E, Jaeken, J, Den Tandt, W, Harvengt, L, Delhaye, J, Deloecker, W
Foilsithe / Cruthaithe 1975