Zobrazeno 1 - 10
of 64
pro vyhledávání: '"K W Kastrup"'
Autor:
K W Kastrup
Publikováno v:
Acta Paediatrica. 77:43-46
Oestradiol stimulates growth and development in Turner's syndrome. Previous results with low-dose oestradiol on growth rate are reviewed. The effect of oestradiol in low concentrations on somatomedin generation, GH secretion and directly on osseous t
Autor:
Anders Juul, Ole Lander Svendsen, Ulla Feldt-Rasmussen, Martin Lange, K W Kastrup, Jørn Müller
Publikováno v:
Capital Region of Denmark
The aim was to reevaluate a group of adults treated for idiopathic childhood onset GH deficiency (GHD) after 18 yr without GH treatment. Twenty-six (11 females) patients participated. All but two had isolated GHD. Childhood diagnosis was established
Autor:
Jens Otto Lunde Jørgensen, Rune Weis Naeraa, Kim Brixen, Claus Højbjerg Gravholt, Jens Sandahl Christiansen, K. W. Kastrup, Leif Mosekilde
Publikováno v:
Pediatrics. 110:889-896
Background. Most girls with Turner syn- drome (TS) receive growth hormone (GH) treatment dur- ing childhood and adolescence, but controlled data on the effects on body composition and glucose metabolism are lacking. Objective. To study the effects of
Autor:
Jørn Müller, Søren A. Pedersen, Jens H. Henriksen, Sören Möller, K W Kastrup, Susanne Rasmussen, Niels E. Skakkebæk, Jehangir Mistry, Anders Juul, Eva Mosfeldt-Laursen, Herbert Yu, Michael Højby Rasmussen, Thomas H. Scheike
Publikováno v:
Scopus-Elsevier
Circulating insulin-like growth factor-I (IGF-I) is predominantly bound in the trimeric complex comprised of IGF binding protein-3 (IGFBP-3) and acid-labile subunit (ALS). Circulating concentrations of IGF-I, IGFBP-3 and ALS are believed to reflect t
Autor:
Jørn Müller, Anders Juul, Kim F. Michaelsen, Niels E. Skakkebæk, Søren A. Pedersen, Thomas H. Scheike, Susanne Rasmussen, K W Kastrup, Kirsten Holm
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:2497-2502
Serum levels of total insulin-like growth factor I (IGF-I) and IGF-binding protein-3 (IGFBP-3) reflect endogenous GH secretion in healthy children, which makes them good diagnostic markers for screening of GH deficiency (GHD) in short children, altho
Publikováno v:
European Journal of Pediatrics. 153:72-77
Girls with Turner syndrome are mainly characterized by growth retardation and gonadal insufficiency. In order to evaluate the effect of growth hormone (GH) and/or low dose 17 beta-oestradiol (E2) on growth and pubertal development, 39 Turner girls wi
Autor:
Niels E. Skakkebæk, Kim F. Michaelsen, J. T. Jørgensen, Henrik B. Mortensen, K W Kastrup, Katharina M. Main
Publikováno v:
Acta Paediatrica. 80:1150-1157
Fifteen prepubertal short stature children (10 girls, 5 boys), mean age 9.6 years (range 5.2-12.7 years), with normal response to growth hormone stimulation tests (group A) or partial growth hormone deficiency (GHD) of idiopathic nature (group B) wer
Autor:
Ulla Feldt-Rasmussen, Jørn Müller, Martin Lange, Ole Lander Svendsen, K W Kastrup, Anders Juul
Publikováno v:
Clinical endocrinology. 62(1)
Objective Despite seemingly adequate growth hormone (GH) treatment during childhood, children with GH deficiency (GHD) have reduced bone mineral density (BMD) at final height. The aim was to evaluate BMD and bone mineral content (BMC) in adults treat
Autor:
K W, Kastrup, K V, Andersen
Publikováno v:
Ugeskrift for laeger. 163(12)