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Browsing by Author Wit, J.M.

Full Text	Issue Date	Title	Author(s)
	2012	IGF1, IGF1R and SHOX mutation analysis in short children born small for gestational age and short children with normal birth size (idiopathic short stature).	Caliebe, J.; Broekman, S.; Boogaard, M.W. van den, et al
	2009	Intelligence of very preterm or very low birthweight infants in young adulthood.	Weisglas-Kuperus, N.; Hille, E.T.; Duivenvoorden, H.J., et al
	1995	Long-term results of growth hormone therapy in children with short stature, subnormal growth rate and normal growth hormone respons to secretagogues	Wit, J.M.; Boersma, B.; Muinck Keizer-Schrama, S.M.P.F. de, 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
	2008	Mental and motor development before and during growth hormone treatment in infants and toddlers with Prader-Willi syndrome.	Festen, D.A.; Wevers, M.; Lindgren, A.C., et al
	2010	Pediatric oncologists' attitudes towards involving adolescents in decision-making concerning research participation.	Vries, M.C. de; Wit, J.M.; Engberts, D.P., et al
	2007	Psychomotor development in infants with Prader-Willi syndrome and associations with sleep-related breathing disorders.	Festen, D.A.; Wevers, M.; Weerd, A.W. de, et al
	1996	PT-1: Clinical aspects	Pfaffle, R.W.; Kim, C.; Otten, B.J., et al
	2008	Randomized controlled GH trial: effects on anthropometry, body composition and body proportions in a large group of children with Prader-Willi syndrome.	Festen, D.A.; Wijngaarden, R. de Lind van; Eekelen, Marielle van, et al
	2008	Screening rules for growth to detect celiac disease: a case-control simulation study.	Dommelen, P van; Grote, F.K.; Oostdijk, W., et al
	2011	The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated protein	Duyvenvoorde, H.A. van; Doorn, J. van; Koenig, J., et al
	2010	Short stature associated with a novel heterozygous mutation in the insulin-like growth factor 1 gene.	Duyvenvoorde, H.A. van; Setten, P.A. van; Walenkamp, M.J., et al
	2007	Thyroid hormone levels in children with Prader-Willi syndrome before and during growth hormone treatment.	Festen, D.A.; Visser, T.J.; Otten, B.J., 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