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Browsing by Author Wit, J.M.

Full Text	Issue Date	Title	Author(s)
	2011	Genome-wide screening in human growth plates during puberty in one patient suggests a role for RUNX2 in epiphyseal maturation.	Emons, J.; Dutilh, B.E.; Decker, E., et al
	2004	Genotype-phenotype correlation in patients suspected of having sotos syndrome.	Boer, L.M.; Kant, S.; Karperien, M., et al
	1997	Growth before and during growth hormone treatment in children operated for craniopharyngioma	Hogeveen, M.; Noordam, C.; Otten, B.J., et al
	1995	Growth hormone treatment in two dose regiments in girls with Turner syndrome: final height results	Massa, G.G.; Otten, B.J.; Muinck Keizer-Schrama, S.M.P.F. de, et al
	2008	Homozygous and heterozygous expression of a novel mutation of the acid-labile subunit.	Duyvenvoorde, H.A. van; Kempers, M.J.E.; Twickler, T.B., et al
	2009	Human acid-labile subunit deficiency: clinical, endocrine and metabolic consequences.	Domene, H.M.; Hwa, V.; Argente, J., 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
	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