Y. Thomasse

Comment on: Prenatal exposure to acid‐suppressive drugs and the risk of allergic disease in the offspring: a cohort study

G. W. Ten Tusscher, A. Sprikkelman, N. Petrus, 2014, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[Three infants with constipation and muscular weakness: infantile botulism].

T. V. van Weerden, J. Arends, Y. Thomasse, 2005, Nederlands tijdschrift voor geneeskunde.

An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions.

N. de Leeuw, C. V. van Ravenswaaij-Arts, T. Dijkhuizen, 2009, European journal of medical genetics.

Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy.

F. Baas, E. Aronica, C. Angelini, 2013, Brain : a journal of neurology.

Hereditary tyrosinemia type I: A new clinical classification with difference in prognosis on dietary treatment

V. Fidler, H. Heymans, P. Clayton, 1994, Hepatology.