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Results: 1-17 |
Results: 17
3-M syndrome: description of six new patients with review of the literature
Authors: van der Wall, G Otten, BJ Brunner, HG van der Burgt, I
Citation: G. Van Der Wall et al., 3-M syndrome: description of six new patients with review of the literature, CLIN DYSMOR, 10(4), 2001, pp. 241-252
Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial
Authors: Noordam, C van der Burgt, I Sengers, RCA Delemarre-van de Waal, HA Otten, BJ
Citation: C. Noordam et al., Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial, ACT PAEDIAT, 90(8), 2001, pp. 889-894
Can GnRH-agonist treatment cause slipped capital femoral epiphysis?
Authors: Kempers, MJE Noordam, C Rouwe, CW Otten, BJ
Citation: Mje. Kempers et al., Can GnRH-agonist treatment cause slipped capital femoral epiphysis?, J PED END M, 14(6), 2001, pp. 729-734
Growth hormone (GH) secretion in children with Noonan syndrome: frequentlyabnormal without consequences for growth or response to GH treatment
Authors: Noordam, C van der Burgt, I Sweep, CGJ Delemarre-van de Waal, HA Sengers, RCA Otten, BJ
Citation: C. Noordam et al., Growth hormone (GH) secretion in children with Noonan syndrome: frequentlyabnormal without consequences for growth or response to GH treatment, CLIN ENDOCR, 54(1), 2001, pp. 53-59
Newborn screening for congenital adrenal hyperplasia in the Netherlands
Authors: Van der Kamp, HJ Noordam, K Elvers, B Van Baarle, M Otten, BJ Verkerk, PH
Citation: Hj. Van Der Kamp et al., Newborn screening for congenital adrenal hyperplasia in the Netherlands, PEDIATRICS, 108(6), 2001, pp. 1320-1324
Genotype versus phenotype in families with androgen insensitivity syndrome
Authors: Boehmer, ALM Bruggenwirth, H Van Assendelft, C Otten, BJ Verleun-Mooijman, MCT Niermeijer, MF Brunner, HG Rouwe, CW Waelkens, JJ Oostdijk, W Kleijer, WJ Van der Kwast, TH De Vroede, MA Drop, SLS
Citation: Alm. Boehmer et al., Genotype versus phenotype in families with androgen insensitivity syndrome, J CLIN END, 86(9), 2001, pp. 4151-4160
Calcaneal ultrasound imaging in healthy children and adolescents: Relationof the ultrasound parameters BUA and SOS to age, body weight, height, footdimensions and pubertal stage
Authors: van den Bergh, JPW Noordam, C Ozyilmaz, A Hermus, ARMR Smals, AGH Otten, BJ
Citation: Jpw. Van Den Bergh et al., Calcaneal ultrasound imaging in healthy children and adolescents: Relationof the ultrasound parameters BUA and SOS to age, body weight, height, footdimensions and pubertal stage, OSTEOPOR IN, 11(11), 2000, pp. 967-976
Maternal uniparental disomy 7 - review and further delineation of the phenotype
Authors: Kotzot, D Balmer, D Baumer, A Chrzanowska, K Hamel, BCJ Ilyina, H Krajewska-Walasek, M Lurie, IW Otten, BJ Schoenle, E Tariverdian, G Schinzel, A
Citation: D. Kotzot et al., Maternal uniparental disomy 7 - review and further delineation of the phenotype, EUR J PED, 159(4), 2000, pp. 247-256
Final height after gonadotrophin releasing hormone agonist treatment for central precocious puberty: The Dutch experience
Authors: Mul, D Oostdijk, W Otten, BJ Rouwe, C Jansen, M Delemarre-van de Waal, HA Waelkens, JJJ Drop, SLS
Citation: D. Mul et al., Final height after gonadotrophin releasing hormone agonist treatment for central precocious puberty: The Dutch experience, J PED END M, 13, 2000, pp. 765-772
Immunological tolerance in an HLA non-identical chimeric twin (vol 61, pg 190, 2000)
Authors: Vietor, HE Hamel, BCJ van Bree, SPMJ van der Meer, EMW Smeets, DFCM Otten, BJ Holl, RA Claas, FHJ
Citation: He. Vietor et al., Immunological tolerance in an HLA non-identical chimeric twin (vol 61, pg 190, 2000), HUMAN IMMUN, 61(7), 2000, pp. 720-720
Immunological tolerance in an HLA non-identical chimeric twin
Authors: Vietor, HE Hamel, BCJ van Bree, SPMJ van der Meer, EMW Smeets, DFCM Otten, BJ Holl, RA Claas, FHJ
Citation: He. Vietor et al., Immunological tolerance in an HLA non-identical chimeric twin, HUMAN IMMUN, 61(3), 2000, pp. 190-192
Radial defects and testicular dysfunction: a new syndrome?
Authors: Tuerlings, JHAM Otten, BJ Hamilton, CJCM Brunner, HG
Citation: Jham. Tuerlings et al., Radial defects and testicular dysfunction: a new syndrome?, CLIN DYSMOR, 8(3), 1999, pp. 203-205
Influence of peritoneal loss of GHBP, IGF-I and IGFBP-3 on serum levels inchildren with ESRD
Authors: van der Kamp, HJ Otten, BJ Swinkels, LMJW Sweep, CGJ Monnens, LAH Schroder, CH
Citation: Hj. Van Der Kamp et al., Influence of peritoneal loss of GHBP, IGF-I and IGFBP-3 on serum levels inchildren with ESRD, NEPH DIAL T, 14(1), 1999, pp. 257-258
Precocious puberty in boys.
Authors: Brunner, HG Otten, BJ
Citation: Hg. Brunner et Bj. Otten, Precocious puberty in boys., N ENG J MED, 341(23), 1999, pp. 1763-1765
A limited repertoire of mutations of the luteinizing hormone (LH) receptorgene in familial and sporadic patients with male LH-independent precociouspuberty
Authors: Kremer, H Martens, JWM van Reen, M Verhoef-Post, M Wit, JM Otten, BJ Drop, SLS Delemarre-van de Waal, HA Pombo-Arias, M De Luca, F Potau, N Buckler, JMH Jansen, M Parks, JS Latif, HA Moll, GW Epping, W Saggese, G Mariman, ECM Themmen, APN Brunner, HG
Citation: H. Kremer et al., A limited repertoire of mutations of the luteinizing hormone (LH) receptorgene in familial and sporadic patients with male LH-independent precociouspuberty, J CLIN END, 84(3), 1999, pp. 1136-1140
Normalization of height in girls with Turner syndrome after long-term growth hormone treatment: Results of a randomized dose-response trial
Authors: Sas, TCJ Keizer-Schrama, SMPFD Stijnen, T Jansen, M Otten, BJ Hoorweg-Nijman, JJG Vulsma, T Massa, GG Rouwe, CW Reeser, HM Gerver, WJ Gosen, JJ Rongen-Westerlaken, C Drop, SLS
Citation: Tcj. Sas et al., Normalization of height in girls with Turner syndrome after long-term growth hormone treatment: Results of a randomized dose-response trial, J CLIN END, 84(12), 1999, pp. 4607-4612
17 beta-hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations
Authors: Boehmer, ALM Brinkmann, AO Sandkuijl, LA Halley, DJJ Niermeijer, MF Andersson, S de Jong, FH Kayserili, H de Vroede, MA Otten, BJ Rouwe, CW Mendonca, BB Rodrigues, C Bode, HH de Ruiter, PE Delemarre-van de Waal, HA Drop, SLS
Citation: Alm. Boehmer et al., 17 beta-hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations, J CLIN END, 84(12), 1999, pp. 4713-4721
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