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Results: 1-12 |
Results: 12
Growth hormone deficiency in Prader-Willi syndrome
Authors: Eiholzer, U Bachmann, S L'Allemand, D
Citation: U. Eiholzer et al., Growth hormone deficiency in Prader-Willi syndrome, ENDOCRINOLO, 10(4), 2000, pp. 50S-56S
Consensus statement - Prader-Willi syndrome: Growth hormone (GH)/insulin-like growth factor axis deficiency and GH treatment
Authors: Lee, PDK Allen, DB Angulo, MA Cappa, M Carrel, AL Castro-Magana, M Chiumello, G Davies, PSW Eiholzer, U Grugni, G Hauffa, BP Hintz, RL Lammer, C Mogul, HR Myers, SE Partsch, CJ Pescovitz, OH Ritzen, EM Rosenfeld, RG Sipila, I Wilson, DM
Citation: Pdk. Lee et al., Consensus statement - Prader-Willi syndrome: Growth hormone (GH)/insulin-like growth factor axis deficiency and GH treatment, ENDOCRINOLO, 10(4), 2000, pp. 71S-73S
Does growth hormone therapy improve motor development in infants with Prader-Willi syndrome?
Authors: Eiholzer, U Malich, S I'Allemand, D
Citation: U. Eiholzer et al., Does growth hormone therapy improve motor development in infants with Prader-Willi syndrome?, EUR J PED, 159(4), 2000, pp. 299-299
Cardiovascular risk factors improve during 3 years of growth hormone therapy in Prader-Willi syndrome
Authors: l'Allemend, D Eiholzer, U Schlumpf, M Steinert, H Riesen, W
Citation: D. L'Allemend et al., Cardiovascular risk factors improve during 3 years of growth hormone therapy in Prader-Willi syndrome, EUR J PED, 159(11), 2000, pp. 835-842
Symptomatic versus substitution growth hormone therapy in short children: From auxology towards a comprehensive multidimensional assessment of short stature and related interventions
Authors: Haverkamp, F Eiholzer, U Ranke, MB Noeker, M
Citation: F. Haverkamp et al., Symptomatic versus substitution growth hormone therapy in short children: From auxology towards a comprehensive multidimensional assessment of short stature and related interventions, J PED END M, 13(4), 2000, pp. 403-408
Growth hormone normalises height, prediction of final height and hand length in children with Prader-Willi syndrome after 4 years of therapy
Authors: Eiholzer, U l'Allemand, D
Citation: U. Eiholzer et D. L'Allemand, Growth hormone normalises height, prediction of final height and hand length in children with Prader-Willi syndrome after 4 years of therapy, HORMONE RES, 53(4), 2000, pp. 185-192
Body composition abnormalities in children with Prader-Willi syndrome and long-term effects of growth hormone therapy
Authors: Eiholzer, U l'Alleman, D van der Sluis, I Steinert, H Gasser, T Ellis, K
Citation: U. Eiholzer et al., Body composition abnormalities in children with Prader-Willi syndrome and long-term effects of growth hormone therapy, HORMONE RES, 53(4), 2000, pp. 200-206
Is there growth hormone deficiency in Prader-Willi syndrome? - Six arguments to support the presence of hypothalamic growth hormone deficiency in Prader-Willi syndrome
Authors: Eiholzer, U Bachmann, S I'Allemand, D
Citation: U. Eiholzer et al., Is there growth hormone deficiency in Prader-Willi syndrome? - Six arguments to support the presence of hypothalamic growth hormone deficiency in Prader-Willi syndrome, HORMONE RES, 53, 2000, pp. 44-52
Phenotypic heterogeneity of growth and psychometric intelligence in Prader-Willi syndrome: Variable expression of a contiguous gene syndrome or parent-child resemblance?
Authors: Malich, S Largo, RH Schinzel, A Molinari, L Eiholzer, U
Citation: S. Malich et al., Phenotypic heterogeneity of growth and psychometric intelligence in Prader-Willi syndrome: Variable expression of a contiguous gene syndrome or parent-child resemblance?, AM J MED G, 91(4), 2000, pp. 298-304
Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine
Authors: Pannain, S Feldman, M Eiholzer, U Weiss, RE Scherberg, NH Refetoff, S
Citation: S. Pannain et al., Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine, J CLIN END, 85(8), 2000, pp. 2786-2792
Male hypogonadism caused by homozygous deletion of exon 10 of the luteinizing hormone (LH) receptor: Differential action of human chorionic gonadotropin and LH
Authors: Gromoll, J Eiholzer, U Nieschlag, E Simoni, M
Citation: J. Gromoll et al., Male hypogonadism caused by homozygous deletion of exon 10 of the luteinizing hormone (LH) receptor: Differential action of human chorionic gonadotropin and LH, J CLIN END, 85(6), 2000, pp. 2281-2286
Body fat determined by skinfold measurements is elevated despite underweight in infants with Prader-Labhart-Willi syndrome
Authors: Eiholzer, U Blum, WF Molinari, L
Citation: U. Eiholzer et al., Body fat determined by skinfold measurements is elevated despite underweight in infants with Prader-Labhart-Willi syndrome, J PEDIAT, 134(2), 1999, pp. 222-225
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