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Browsing by Author Trotsenburg, A.S. van
Showing results 1 to 5 of 5
| Full Text | Issue Date | Title | Author(s) | | 2011 | Familial neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin II gene | Fost, M. de; Trotsenburg, A.S. van; Santen, H.M. van; Endert, E.; Elzen, C. van den, et al |
| 2010 | Efficacy and safety of oxandrolone in growth hormone-treated girls with turner syndrome. | Menke, L.A.; Sas, T.C.J.; Muinck Keizer-Schrama, S.M.P.F. de; Zandwijken, G.R.; Ridder, M.A. de, et al |
| 2009 | Efficacy and safety of long-term continuous growth hormone treatment in children with Prader-Willi syndrome. | Lind van Wijngaarden, R.F. de; Siemensma, E.P.; Festen, D.A.; Otten, B.J.; Mil, E.G. van, et al |
| 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., 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; Trotsenburg, A.S. van; Wiedijk, B.M., et al |
Showing results 1 to 5 of 5
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