Family with autosomal dominant hyperinsulinism associated with A456V mutation in the glucokinase gene von Dullaart, R.P.F., Hoogenberg, K., Rouwé, C W., Stulp, B. K.

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Genotype versus phenotype in families with androgen insensitivity syndrome von BOEHMER, Annemie L. M, BRÜGGENWIRTH, Hennie, KLEIJER, Wim J, VAN DER KWAST, Theo H, DE VROEDE, Monique A, DROP, Stenvert L. S, VAN ASSENDELFT, Cissy, OTTEN, Barto J, VERLEUN-MOOIJMAN, Marja C. T, NIERMEIJER, Martinus F, BRUNNER, Han G, ROUWE, Catrienus W, WAELKENS, J. J, OOSTDIJK, Wilma

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Normalization of height in girls with Turner syndrome after long-term growth hormone treatment: Results of a randomized dose-response trial von SAS, T. C. J, DE MUINCK KEIZER-SCHRAMA, S. M. P. F, GERVER, W.-J, GOSEN, J. J, RONGEN-WESTERLAKEN, C, DROP, S. L. S, STIJNEN, T, JANSEN, M, OTTEN, B. J, HOORWEG-NIJMAN, J. J. G, VULSMA, T, MASSA, G. G, ROUWE, C. W, REESER, H. M

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Total thyroidectomy in the treatment of thyroid carcinoma in childhood von Stael, A. P. M., Plukker, J. Th. M., Piers, D. A., Rouwé, C. W., Vermey, A.

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In utero diagnosis and treatment of fetal goitrous hypothyroidism, caused by maternal use of propylthiouracil von Van Loon, Aren J., Derksen, Joke Th. M., Bos, Arie F., Rouw, Catrienus W.

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Kinetics and metabolism of 11-deoxycortisol in a patient with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency von Kraan, G.P.B., van Wee, C.J., Wolthers, B.G., Rouwé, C.W., Drayer, N.M., de Bruin, R.

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Yearly stepwise increments of the growth hormone dose results in a better growth response after four years in girls with Turner syndrome von VAN TEUNENBROEK, A, DE MUINCK KEIZER-SCHRAMA, S. M. P. F, GOSEN, J. J, RONGEN-WESTERLAKEN, C, DROP, SITJNEN, T, JANSEN, M, OTTEN, B. J, DELEMARRE-VAN DE WAAL, H. A, VULSMA, T, WIT, J. M, ROUWE, C. W, REESER, H. M

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Final Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment in Three Dosages and Low Dose Estrogens von 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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Effect of Discontinuation of Long-Term Growth Hormone Treatment on Carbohydrate Metabolism and Risk Factors for Cardiovascular Disease in Girls with Turner Syndrome von van Pareren, Yvonne K., de Muinck Keizer-Schrama, Sabine M. P. F., Stijnen, Theo, Sas, Theo C. J., Drop, Stenvert L. S.

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17β-Hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de Novo mutations von BOEHMER, A. L. M, BRINKMANN, A. O, ROUWE, C. W, MENDONCA, B. B, RODRIGUES, C, BODE, H. H, DE RUITER, P. E, DE WAAL, H. A. D.-V, DROP, S. L. S, SANDKUIJL, L. A, HALLEY, D. J. J, NIERMEIJER, M. F, ANDERSSON, S, DE JONG, F. H, KAYSERILI, H, DE VROEDE, M. A, OTTEN, B. J

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Urinary steroid profile of a newborn suffering from pseudohypoaldosteronism von Wolthers, B.G., Kraan, G.P.B., van der Molen, J.C., Nagel, G.T., Rouwe, C.W., Lenting, F., Boersma, E.R.

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Surgical experience in children with differentiated thyroid carcinoma von Haveman, Jan Willem, van Tol, Karin M, Rouwé, Catrienus W, Piers, Do A, Plukker, John T M

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Reduction of excessive height in boys by bilateral percutaneous epiphysiodesis around the knee von ODINK, Roelof J, GERVER, Willem Jan, HEEG, Minne, ROUWE, Catrienus W, VAN WAARDE, Willie M. Bakker, SAUER, Pieter J

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17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations von Boehmer, A L, Brinkmann, A O, Sandkuijl, L A, Halley, D J, Niermeijer, M F, Andersson, S, de Jong, F H, Kayserili, H, de Vroede, M A, Otten, B J, Rouwé, C W, Mendonça, B B, Rodrigues, C, Bode, H H, de Ruiter, P E, Delemarre-van de Waal, H A, Drop, S L

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Yearly stepwise increments of the growth hormone dose results in a better growth response after four years in girls with Turner syndrome. Dutch Working Group on Growth Hormone von van Teunenbroek, A, de Muinck Keizer-Schrama, S M, Stijnen, T, Jansen, M, Otten, B J, Delemarre-van de Waal, H A, Vulsma, T, Wit, J M, Rouwé, C W, Reeser, H M, Gosen, J J, Rongen-Westerlaken, C, Drop, S L

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Yearly stepwise increments of the growth hormone dose results in a better growth response after four years in girls with Turner syndrome. Dutch Working Group on Growth Hormone von van Teunenbroek, A, de Muinck Keizer-Schrama, S M, Stijnen, T, Jansen, M, Otten, B J, Delemarre-van de Waal, H A, Vulsma, T, Wit, J M, Rouwé, C W, Reeser, H M, Gosen, J J, Rongen-Westerlaken, C, Drop, S L

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Genotype Versus Phenotype in Families with Androgen Insensitivity Syndrome von Boehmer, Annemie L. M., Brüggenwirth, Hennie, van Assendelft, Cissy, Otten, Barto J., Verleun-Mooijman, Marja C. T., Niermeijer, Martinus F., Brunner, Han G., Rouwé, Catrienus W., Waelkens, J. J., Oostdijk, Wilma, Kleijer, Wim J., van der Kwast, Theo H., de Vroede, Monique A., Drop, Stenvert L. S.

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Reduction of adult height in childhood acute lymphoblastic leukemia survivors after prophylactic cranial irradiation von Bongers, M.E.J., Francken, A.B., Rouwé, C., Kamps, W.A., Postma, A.

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Final height in central precocious puberty after long term treatment with a slow release GnRH agonist von Oostdijk, W, Rikken, B, Schreuder, S, Otten, B, Odink, R, Rouwé, C, Jansen, M, Gerver, W J, Waelkens, J, Drop, S

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Postprandial chylomicron clearance rate in late teenagers with diabetes mellitus type 1 von VAN WAARDE, Willie M, ODINK, Roel J, ROUWE, Catrienus, STELLAARD, Frans, WESTERS, Mariska, VONK, Roel J, SAUER, Pieter J. J, VERKADE, Henkjan J

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