Search Results - Stokvis-Brantsma, WH

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  1. 1
    Final Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment in Three Dosages and Low Dose Estrogens

    Final Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment in Three Dosages and Low Dose Estrogens by van Pareren, Yvonne K., de Muinck Keizer-Schrama, Sabine M. P. F., Stijnen, Theo, Sas, Theo C. J., Jansen, Maarten, Otten, Barto J., Hoorweg-Nijman, J. J. Gera, Vulsma, Thomas, Stokvis-Brantsma, Wilhelmina H., Rouwé, Catrienus W., Reeser, H. Maarten, Gerver, Willem-Jan, Gosen, Jos J., Rongen-Westerlaken, Ciska, Drop, Stenvert L. S.

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  2. 2
    GH treatment and its effect on bone mineral density, bone maturation and growth in short children born small for gestational age: 3-year results of a randomized, controlled GH trial

    GH treatment and its effect on bone mineral density, bone maturation and growth in short children born small for gestational age: 3-year results of a randomized, controlled GH tria... by Arends, N. J. T., Boonstra, V. H., Mulder, P. G. H., Odink, R. J. H., Stokvis-Brantsma, W. H., Rongen-Westerlaken, C., Mulder, J. C., Delemarre-Van de Waal, H., Reeser, H. M., Jansen, M., Waelkens, J. J. J., Hokken-Koelega, A. C. S.

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  3. 3
    Growth hormone (GH) secretion in patients with an inactivating defect of the GH-releasing hormone (GHRH) receptor is pulsatile: evidence for a role for non-GHRH inputs into the generation of GH pulses

    Growth hormone (GH) secretion in patients with an inactivating defect of the GH-releasing hormone (GHRH) receptor is pulsatile: evidence for a role for non-GHRH inputs into the gen... by Roelfsema, F, Biermasz, N R, Veldman, R G, Veldhuis, J D, Frölich, M, Stokvis-Brantsma, W H, Wit, J M

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  4. 4
    Isolated GH deficiency with dominant inheritance : New mutations, new insights

    Isolated GH deficiency with dominant inheritance : New mutations, new insights by BINDER, G, KELLER, E, MIX, M, MASSA, G. G, STOKVIS-BRANTSMA, W. H, WIT, J. M, RANKE, M. B

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  5. 5
    Loss-of-function mutations in the immunoglobulin superfamily member 1 gene ( IGSF1 ) cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement

    Loss-of-function mutations in the immunoglobulin superfamily member 1 gene ( IGSF1 ) cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement by Schoenmakers, N, Dr, Sun, Y, Bak, B, van Trotsenburg, ASP, Oostdijk, W, Voshol, P, Cambridge, E, White, JK, le Tissier, P, Gharavy, SNM, Martinez-Barbera, JP, Stokvis-Brantsma, WH, Vulsma, T, Kempers, MJ, Persani, L, Campi, I, Bonomi, M, Beck-Peccoz, P, Zhu, H, Davis, TME, Hokken-Koelega, ACS, Del Blanco, D Gorbenko, Rangasami, JJ, Ruivenkamp, CAL, Laros, JFJ, Kriek, M, Kant, SG, Bosch, CAJ, Biermasz, NR, Appelman-Dijkstra, NM, Corssmit, EP, Hovens, GCJ, Pereira, AM, den Dunnen, JT, Wade, MG, Breuning, MH, Hennekam, RC, Dattani, MT, Wit, JM, Bernard, DJ, Chatterjee, K

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