Growth hormone (GH) treatment has been used in children with intrauterine growth retardation (IUGR) to promote growth with success in several short- and long-term clinical trials. Intermittent GH therapy has also been advocated in children with IUGR. This study was designed to evaluate the growth of children with IUGR after discontinuation of a two-year trial of GH treatment. Sixteen children (12 F, 4 M) who had received GH (Genotropin(R)) at age 5.3 (1.3) years at a dose of 0.2 IU/kg/day for 2 years (Group 1) and 10 (6 F, 4 M) controls of age 4.3 (1.7) years without treatment (Group 2) were followed after completion of the trial over a median period of 4 years. Height SDS of the GH-treated group showed an increase from -3.0 (0.5) to -1.9 (...
textabstractWe assessed the effectiveness and safety of 3 yr combined GH and GnRH agonist ...
OBJECTIVE: Data on the GH-induced catch-up growth of severely GH-deficient children affected by mono...
GH is often used to treat children with idiopathic short stature despite the lack of definitive, lon...
textabstractObjective: To assess the long-term effect of prepubertal high-dose GH treatment on growt...
Recombinant human GH therapy to children with idiopathic short stature (ISS) increases growth veloci...
Recombinant human growth hormone (GH) has been used to increase growth and adult height in children ...
Although recombinant techniques have enabled the production of limitless amounts of human growth hor...
BACKGROUND: In recent years, several studies have been published showing different responses to gro...
The growth-promoting effect of continuous GH treatment was eval-uated over 5 yr in 79 children with ...
OBJECTIVE: To investigate which pretreatment variables most significantly affect long-term growth re...
Abstract Background Growth hormone deficiency (GHD) is the commonest endocrine cause of short statur...
Item does not contain fulltextRecombinant human GH therapy to children with idiopathic short stature...
Biologically inactive growth hormone (GH) due to genetic mutations is a rare cause of short stature,...
Forty prepubertal subjects (25 boys and 15 girls) with idiopathic short stature, aged 3.8–14.6 yr, w...
Cushing's disease is associated with growth failure in childhood and adolescence. Growth and final h...
textabstractWe assessed the effectiveness and safety of 3 yr combined GH and GnRH agonist ...
OBJECTIVE: Data on the GH-induced catch-up growth of severely GH-deficient children affected by mono...
GH is often used to treat children with idiopathic short stature despite the lack of definitive, lon...
textabstractObjective: To assess the long-term effect of prepubertal high-dose GH treatment on growt...
Recombinant human GH therapy to children with idiopathic short stature (ISS) increases growth veloci...
Recombinant human growth hormone (GH) has been used to increase growth and adult height in children ...
Although recombinant techniques have enabled the production of limitless amounts of human growth hor...
BACKGROUND: In recent years, several studies have been published showing different responses to gro...
The growth-promoting effect of continuous GH treatment was eval-uated over 5 yr in 79 children with ...
OBJECTIVE: To investigate which pretreatment variables most significantly affect long-term growth re...
Abstract Background Growth hormone deficiency (GHD) is the commonest endocrine cause of short statur...
Item does not contain fulltextRecombinant human GH therapy to children with idiopathic short stature...
Biologically inactive growth hormone (GH) due to genetic mutations is a rare cause of short stature,...
Forty prepubertal subjects (25 boys and 15 girls) with idiopathic short stature, aged 3.8–14.6 yr, w...
Cushing's disease is associated with growth failure in childhood and adolescence. Growth and final h...
textabstractWe assessed the effectiveness and safety of 3 yr combined GH and GnRH agonist ...
OBJECTIVE: Data on the GH-induced catch-up growth of severely GH-deficient children affected by mono...
GH is often used to treat children with idiopathic short stature despite the lack of definitive, lon...