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Full Text	Issue Date	Title	Author(s)
	2012	Evaluation of cognitive and motor development in toddlers with congenital hypothyroidism diagnosed by neonatal screening	van der Sluijs Veer, L.; Kempers, M.J.; Wiedijk, B.M.; Last, B.F.; Grootenhuis, M.A.; Vulsma, T.
	2012	Health- related quality of life and self-worth in 10-year old children with congenital hypothyroidism diagnosed by neonatal screening	van der Sluijs Veer, L.; Kempers, M.J.; Maurice-Stam, H.; Last, B.F.; Vulsma, T.; Grootenhuis, M.A.
	2012	Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm.	Lindsay, M.E.; Schepers, D.; Bolar, N.A.; Doyle, J.J.; Gallo, E.; Fert-Bober, J.; Kempers, M.J.E.; Fishman, E.K.; Chen, Y.; Myers, L.; Bjeda, D.; Oswald, G.; Elias, A.F.; Levy, H.P.; Anderlid, B.M.; Yang, M.H.; Bongers, M.H.F.; Timmermans, J.; Braverman, A.C.; Canham, N.; Mortier, G.R.; Brunner, H.G.; Byers, P.H.; Eyk, J. Van; Laer, L. van; Dietz, H.C.; Loeys, B.L.
	2012	Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement	Sun, Y; Bak, B.; Schoenmakers, N.; van Trotsenburg, A.S.; Oostdijk, W.; Voshol, P.; Cambridge, E.; White, J.K.; le Tissier, P.; Gharavy, S.N.; Martinez-Barbera, J.P.; Stokvis-Brantsma, W.H.; Vulsma, T.; Kempers, M.J.; Persani, L.; Campi, I.; Bonomi, M.; Beck-Peccoz, P.; Zhu, H.; Davis, T.M.; Hokken-Koelega, A.C.; Del Blanco, D.G.; Rangasami, J.J.; Ruivenkamp, C.A.; Laros, J.F.; Kriek, M.; Kant, S.G.; Bosch, C.A.; Biermasz, N.R.; Appelman-Dijkstra, N.M.; Corssmit, E.P.; Hovens, G.C.; Pereira, A.M.; Dunnen, J.T. den; Wade, M.G.; Breuning, M.H.; Hennekam, R.C.; Chatterjee, K.; Dattani, M.T.; Wit, J.M.; Bernard, D.J.
	2012	Inflammation aggravates disease severity in Marfan syndrome patients.	Radonic, T.; Witte, P. de; Groenink, M.; Waard, V. de; Lutter, R.; Eijk, M. van; Jansen, J.L.M.; Timmermans, J.; Kempers, M.J.; Scholte, A.J.H.A.; Hilhorst-Hofstee, Y.; Berg, M.P van den; Tintelen, J.P. van; Pals, G.; Baars, M.J.; Mulder, B.J.; Zwinderman, A.H.
	2012	Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency	Krone, N.; Reisch, N.; Idkowiak, J.; Dhir, V.; Ivison, H.E.; Hughes, B.A.; Rose, I.T.; O'Neil, D.M.; Vijzelaar, R.; Smith, M.J.; Macdonald, F.; Cole, T.R.; Adolphs, N.; Barton, J.S.; Blair, E.M.; Braddock, S.R.; Collins, F.; Cragun, D.L.; Dattani, M.T.; Day, R.; Dougan, S.; Feist, M.; Gottschalk, M.E.; Gregory, J.W.; Haim, M.; Harrison, R.; Olney, A.H.; Hauffa, B.P.; Hindmarsh, P.C.; Hopkin, R.J.; Jira, P.E.; Kempers, M.J.; Kerstens, M.N.; Khalifa, M.M.; Kohler, B.; Maiter, D.; Nielsen, S.; O'Riordan, S.M.; Roth, C.L.; Shane, K.P.; Silink, M.; Stikkelbroeck, N.; Sweeney, E.; Szarras-Czapnik, M.; Waterson, J.R.; Williamson, L.; Hartmann, M.F.; Taylor, N.F.; Wudy, S.A.; Malunowicz, E.M.; Shackleton, C.H.; Arlt, W.
	2011	Effects of naproxen and sulphasalazine or methotrexate on hypothalamic-pituitary-adrenal axis activity in patients with rheumatoid arthritis	Eijsbouts, A.M.M.; Kempers, M.J.E.; Hoogen, F.H. Van den; Laan, R.F.J.M.; Hermus, A.R.M.M.; Ross, H.A.; Sweep, F.C.; Putte, L.B.A. van de
	2011	Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study	Kempers, M.J.E.; Kuiper, R.P.; Ockeloen, C.W.; Chappuis, P.O.; Hutter, P.; Rahner, N.; Schackert, H.K.; Steinke, V.; Holinski-Feder, E.; Morak, M.; Kloor, M.; Buttner, R.; Verwiel, E.T.P.; Krieken, J.H. van; Nagtegaal, I.D.; Goossens, M.; Post, R.S. van der; Niessen, R.C.; Sijmons, R.H.; Kluijt, I.; Hogervorst, F.B.L.; Leter, E.M.; Gille, J.J.P.; Aalfs, C.M.; Redeker, E.J.; Hes, F.J.; Tops, C.M.; Nesselrooij, B.P. van; Gijn, M.E. van; Gomez Garcia, E.B.; Eccles, D.M.; Bunyan, D.J.; Syngal, S.; Stoffel, E.M.; Culver, J.O.; Palomares, M.R.; Graham, T.; Velsher, L.; Papp, J.; Olah, E.; Chan, T.L.; Leung, S.Y.; Geurts van Kessel, A.H.M.; Kiemeney, L.A.L.M.; Hoogerbrugge, N.; Ligtenberg, M.J.L.
	2009	Morphological abnormalities in children with thyroidal congenital hypothyroidism.	Kempers, M.J.E.; Ozgen, H.M.; Vulsma, T.; Merks, J.H.; Zwinderman, K.H.; Vijlder, J.J. de; Hennekam, R.C.M.
	2009	Human acid-labile subunit deficiency: clinical, endocrine and metabolic consequences.	Domene, H.M.; Hwa, V.; Argente, J.; Wit, J.M.; Camacho-Hubner, C.; Jasper, H.G.; Pozo, J.; Duyvenvoorde, H.A. van; Yakar, S.; Fofanova-Gambetti, O.V.; Rosenfeld, R.G.; Hermus, A.R.M.M.; Twickler, T.B.; Kempers, M.J.E.
	2009	Effect of naproxen on the hypothalamic-pituitary-adrenal axis in healthy volunteers.	Eijsbouts, A.M.M.; Kempers, M.J.E.; Kramer, R.S.; Hopman, M.T.E.; Hoogen, F.H.J. van den; Laan, R.F.J.M.; Hermus, A.R.M.M.; Sweep, C.G.J.; Putte, L.B.A. van de
	2009	Systematic review: diagnostic procedures to differentiate unilateral from bilateral adrenal abnormality in primary aldosteronism.	Kempers, M.J.E.; Lenders, J.W.M.; Outheusden, L. van; Wilt, G.J. van der; Schultze Kool, L.J.; Hermus, A.R.M.M.; Deinum, J.
	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.; Vulsma, T.; Grootenhuis, M.A.
	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.; Doorn, J. van; Gerver, W.J.; Noordam, C.; Losekoot, M.; Karperien, M.; Wit, J.M.; Hermus, A.R.
	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; Smets, A.M.; Smit, B.J.; Vijlder, J.J. de; Vulsma, T.
	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.; Lanting, C.I.; Kooistra, L.; Wiedijk, B.M.; Last, B.F.; Vijlder, J.J. de; Grootenhuis, M.A.; Vulsma, T.
	2006	[Central congenital hypothyroidism due to Graves' disease in the mother]	Liebrand, C.A.; Mol, A.C. de; Kempers, M.J.E.; Noordam, C.
	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; Trotsenburg, A.S. van; Wiedijk, B.M.; Vijlder, J.J. de; Vulsma, T.
	2006	Intellectual and motor development of young adults with congenital hypothyroidism diagnosed by neonatal screening	Kempers, M.J.E.; Sluijs-Veer, L. van der; Nijhuis-Van der Sanden, M.W.G.; Kooistra, L.; Wiedijk, B.M.; Faber, I.R.; Last, B.F.; Vijlder, J.J. de; Grootenhuis, M.A.; Vulsma, T.

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