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<italic>IGF1</italic> Haploinsufficiency: Phenotype and Response to Growth Hormone Treatment in 9 Patients.

Horm Res Paediatr
Joustra SD, Punt LD, van der Kaay DCM, van Setten PA, de Groote K, Kruijsen AR, Bocca G, de Munnik SA, Renes JS, de Bruin C, Losekoot M, van Duyvenvoorde HA, Wit JM, Joustra SD.   +13 more
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Biosynthetic Human Growth Hormone in the Treatment of Growth Hormone Deficiency

Acta Paediatrica, 1990
ABSTRACT. A total of 309 previously untreated children with growth hormone deficiency (GHD) (219 boys, 90 girls; mean age 8.4 ± 3.9 years, range 1.5‐19 years) were treated for up to 3 years in an ongoing trial designed to examine the long‐term efficacy and safety of biosynthetic somatropin (rhGH).
J H, Holcombe, P M, Conforti, A C, Wong, R G, Thompson, M W, Draper   +4 more
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Robinow Syndrome with Growth Hormone Deficiency: Treatment with Growth Hormone

Journal of Pediatric Endocrinology and Metabolism, 1999
We describe a 5 years and nine months old boy who presented with facial features, vertebral anomalies and dwarfism consistent with Robinow syndrome. Investigations revealed growth hormone (GH) deficiency to be the cause of his dwarfism. We reviewed data on four other patients with Robinow syndrome from the Genentech National Cooperative Growth Study ...
S, Castells, A, Chakurkar, Q, Qazi, W, Bastian   +3 more
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Changes with growth hormone treatment in growth hormone deficient children

Pediatrics International, 1995
AbstractA total of 54 previously untreated patients (15 girls, 39 boys) with poor growth due to idiopathic growth hormone deficiency (IGHD) were treated with human growth hormone (hGH), continuously up to 4 years. All of the patients had a peak hGH level which was below 10 ng/mL after at least two pharmacological tests and/or blunted physiologic hGH ...
G, Ocal, M, Berberoglu, S, Akçurin, N, Memioglu, A, Ikinciogullari   +4 more
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