De novo malignancy after paediatric renal replacement therapy

Por Coutinho, H, Groothoff, J, Offringa, M, Gruppen, M, Heymans, H
Publicado em 2001

Intestinal permeability in relation to birth weight and gestational and postnatal age

Por van Elburg, R M, Fetter, W, Bunkers, C, Heymans, H
Publicado em 2003

Intestinal permeability in patients with coeliac disease and relatives of patients with coeliac disease.

Por van Elburg, R M, Uil, J J, Mulder, C J, Heymans, H S
Publicado em 1993

Impaired cognition and schooling in adults with end stage renal disease since childhood

Por Groothoff, J, Grootenhuis, M, Dommerholt, A, Gruppen, M, Offringa, M, Heymans, H
Publicado em 2002

The effect of brief neonatal exposure to cows' milk on atopic symptoms up to age 5

Por de Jong, M H, Scharp-Van, D, Aalberse, R, Heymans, H, Brunekreef, B
Publicado em 2002

Is encopresis always the result of constipation?

Por Benninga, M A, Büller, H A, Heymans, H S, Tytgat, G N, Taminiau, J A
Publicado em 1994

Use of tracheal auscultation for the assessment of bronchial responsiveness in asthmatic children.

Por Sprikkelman, A. B., Grol, M. H., Lourens, M. S., Gerritsen, J., Heymans, H. S., van Aalderen, W. M.
Publicado em 1996

Platelet-activating factor: mediator of the third pathway of platelet aggregation? A study in three patients with deficient platelet-activating factor synthesis.

Por Sturk, A, Schaap, M C, ten Cate, J W, Heymans, H S, Schutgens, R B, Przyrembel, H, Borst, P
Publicado em 1987

Phenylketonuria. The in vivo hydroxylation rate of phenylalanine into tyrosine is decreased.

Por van Spronsen, F J, Reijngoud, D J, Smit, G P, Nagel, G T, Stellaard, F, Berger, R, Heymans, H S
Publicado em 1998

Prognosis of extrahepatic biliary atresia.

Por Houwen, R H, Zwierstra, R P, Severijnen, R S, Bouquet, J, Madern, G, Vos, A, Bax, N M, Heymans, H S, Bijleveld, C M
Publicado em 1989

Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.

Por Heikoop, J C, van Roermund, C W, Just, W W, Ofman, R, Schutgens, R B, Heymans, H S, Wanders, R J, Tager, J M
Publicado em 1990

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementa...

Por Brul, S, Westerveld, A, Strijland, A, Wanders, R J, Schram, A W, Heymans, H S, Schutgens, R B, van den Bosch, H, Tager, J M
Publicado em 1988

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.

Por Schram, A W, Goldfischer, S, van Roermund, C W, Brouwer-Kelder, E M, Collins, J, Hashimoto, T, Heymans, H S, van den Bosch, H, Schutgens, R B, Tager, J M
Publicado em 1987

eLetters:

Por Host, A, Koletzko, B, Dreborg, S, Muraro, A, Wahn, U, Aggett, P, Bresson, J, Hernell, O, Lafeber, H, Michaelsen, K, Micheli, J, Rigo, J, Weaver, L, Heymans, H, Strobel, S, Vandenplas, Y
Publicado em 1999