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Browsing by Author Vulsma, T.

Full Text	Issue Date	Title	Author(s)
	2007	Loss of integrity of thyroid morphology and function in children born to mothers with inadequately treated Graves' disease.	Kempers, M.J.E.; Trotsenburg, A.S. van; Rijn, R.R. van, et al
	2012	Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement	Sun, Y; Bak, B.; Schoenmakers, N., et al
	2009	Morphological abnormalities in children with thyroidal congenital hypothyroidism.	Kempers, M.J.E.; Ozgen, H.M.; Vulsma, T., et al
	2006	Neonatal screening for congenital hypothyroidism based on thyroxine, thyrotropin, and thyroxine-binding globulin measurement: potentials and pitfalls.	Kempers, M.J.E.; Lanting, C.I.; Heijst, A.F.J. van, et al
	2007	Neonatal screening for congenital hypothyroidism in the Netherlands: cognitive and motor outcome at 10 years of age.	Kempers, M.J.E.; Sluijs-Veer, L. van der; Nijhuis-Van der Sanden, M.W.G., et al
	2008	Quality of life, developmental milestones, and self-esteem of young adults with congenital hypothyroidism diagnosed by neonatal screening.	Veer, L van der Sluijs; Kempers, M.J.E.; Last, B.F., et al
	1996	Yearly stepwise increments of the growth syndrome dose results in a better growth response after four years in girls with Turner Syndrome	Teunenbroek, A. van; Muinck Keizer-Schrama, S.M.P.F. de; Stijnen, T., et al