Show
Sort by
-
La lymphohistiocytose familiale érythrophagocytaire : à propos de cinq observations avec étude cytophotométrique de l'A.D.N. nucléaire
-
A case of retinoblastoma, associated with histiocytosis-X and mosaicism of a deleted D-group chromosome (13q14→q31)
-
Bilateral pneumothorax as an early sign in a child with histiocytosis-X
-
Skeletafwijkingen bij kinderen met acute lymfoblasten leukemie
-
'Malignant lymfoma' with favourable outcome
-
An unusual case of acquired hypolipemia and LCAT deficiency. Proc. 57th European Atherosclerosis Society Congress, Lissabon 1991, p. 90.
-
Zeldzame Tumoren. Hoofdst. 25 in 'Kinderoncologie' - P.A. Voûte, J. de Kraker, H.N. Caron, ed. - Bohn Stafley Van Loghum, Houten, 1997, pp. 334-350.
-
An unusual case of acquired hypolipaemia and LCAT deficiency. Molecular Biology of Atherosclerosis, P-oceedings of the 57th European Atherosclerosis Society Meeting, Ed. M.J. Halpern, John Libbey & Cie Ltd, Chapter 28, 1992, pp. 137-139.