A total of 21 patients with somatotropic deficiency have been enrolled in a clinical trial of biosynthetic growth hormone (bio-GH) and pituitary growth hormone (pit-GH). Five of them not previously treated (naïve) and 7 previously treated with pit-GH, received bio-GH; 9 received only pit-GH. Biosynthetic-GH was given 12 UI/m2/week. Height velocities during treatment rose, for naïve patients, from 3.6 +/- 0.3 cm/year (before treatment) to 8.7 +/- 1.3 cm/year (after 12 months treatment). For previously treated patients, after a period at least 6 months without any GH therapy, the increase in height was from 2.5 +/- 0.9 cm/year to 6.8 cm/year; and for the patients who received only pit-GH was from 3.4 +/- 1.2 cm/year to 8.0 +/- 1.1 cm/year. No...
Girls with Turner syndrome were divided according to age (group A 6-12 years, and group B 12-19 year...
In subjects with an isolated GH deficiency the inhibition of puberty by GnRH-analogue administration...
RASopathies are developmental disorders caused by heterozygous germline mutations in genes encoding ...
A total of 21 patients with somatotropic deficiency have been enrolled in a clinical trial of biosyn...
Until 1985 growth hormone (GH) was obtained from pituitary extracts, and was available in limited am...
18 prepubertal growth-hormone (GH)-deficient children were treated with twice-daily subcutaneous inj...
Growth failure is commonly described in polytransfused thalassaemia major patients (Th) with or with...
Biologically inactive growth hormone (GH) due to genetic mutations is a rare cause of short stature,...
Dana S HardinOhio State University and Columbus Children’s Hospital, Columbus, Ohio, USAAb...
Although recombinant techniques have enabled the production of limitless amounts of human growth hor...
Objective - Impairment of linear growth is a common clinical feature in patients with \u3b2-thalassa...
Recombinant human GH therapy to children with idiopathic short stature (ISS) increases growth veloci...
The availability of recombinant human growth hormone (GH) and the optimization of substitutive thera...
<em>The opportunities of receiving of genetically engineered medications, e.g. somatotropic hormone ...
Item does not contain fulltextRecombinant human GH therapy to children with idiopathic short stature...
Girls with Turner syndrome were divided according to age (group A 6-12 years, and group B 12-19 year...
In subjects with an isolated GH deficiency the inhibition of puberty by GnRH-analogue administration...
RASopathies are developmental disorders caused by heterozygous germline mutations in genes encoding ...
A total of 21 patients with somatotropic deficiency have been enrolled in a clinical trial of biosyn...
Until 1985 growth hormone (GH) was obtained from pituitary extracts, and was available in limited am...
18 prepubertal growth-hormone (GH)-deficient children were treated with twice-daily subcutaneous inj...
Growth failure is commonly described in polytransfused thalassaemia major patients (Th) with or with...
Biologically inactive growth hormone (GH) due to genetic mutations is a rare cause of short stature,...
Dana S HardinOhio State University and Columbus Children&rsquo;s Hospital, Columbus, Ohio, USAAb...
Although recombinant techniques have enabled the production of limitless amounts of human growth hor...
Objective - Impairment of linear growth is a common clinical feature in patients with \u3b2-thalassa...
Recombinant human GH therapy to children with idiopathic short stature (ISS) increases growth veloci...
The availability of recombinant human growth hormone (GH) and the optimization of substitutive thera...
<em>The opportunities of receiving of genetically engineered medications, e.g. somatotropic hormone ...
Item does not contain fulltextRecombinant human GH therapy to children with idiopathic short stature...
Girls with Turner syndrome were divided according to age (group A 6-12 years, and group B 12-19 year...
In subjects with an isolated GH deficiency the inhibition of puberty by GnRH-analogue administration...
RASopathies are developmental disorders caused by heterozygous germline mutations in genes encoding ...