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Publikováno v:
Pediatric Research. 82:796-800
BackgroundIn the neonatal period, the pituitary hormones including prolactin (PRL) and human growth hormone (hGH) are secreted in high amounts due to immature feedback mechanisms. As both hormones are secreted in part by the same somatomammotrophic c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbd111f9bcafbb668a80d66d87a15dbd
https://doi.org/10.1038/pr.2017.164
https://doi.org/10.1038/pr.2017.164
Publikováno v:
The Israel Medical Association journal : IMAJ. 21(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7ac5fba64d64f011c7d00bb12fb86ce
https://pubmed.ncbi.nlm.nih.gov/31529941
https://pubmed.ncbi.nlm.nih.gov/31529941
Publikováno v:
The Israel Medical Association journal : IMAJ. 21(3)
Treatment of patients with childhood growth hormone deficiency is usually terminated at the end of puberty. Follow-up into adult age is rare, even more so in patients with congenital isolated growth hormone deficiency (cIGHD).To assess the clinical a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8a992420685c646a832a3a5dfebca21
https://pubmed.ncbi.nlm.nih.gov/30905105
https://pubmed.ncbi.nlm.nih.gov/30905105
Publikováno v:
Growth Hormone & IGF Research. 27:46-52
Congenital MPHD is a rare condition caused by mutations in pituitary transcription factors genes: PROP1, POU1F1 (PIT1), HESX1, LHX3, LHX4.We evaluated in a retrospective study the effects on growth and development in 29 patients with congenital MPHD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e24edce7031ffc913e87e42961401541
https://doi.org/10.1016/j.ghir.2016.01.004
https://doi.org/10.1016/j.ghir.2016.01.004
Publikováno v:
Anthropologischer Anzeiger; Bericht uber die biologisch-anthropologische Literatur. 76(2)
The relationship between the length of the second and fourth ring finger (2D:4D ratio) is a sexually dimorphic trait, higher in females than in males. It is established during early prenatal development under the influence of sex hormones, as demonst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14b9f5b8002d5f24505edb69c1599fcd
https://pubmed.ncbi.nlm.nih.gov/30816406
https://pubmed.ncbi.nlm.nih.gov/30816406
Publikováno v:
Pediatric endocrinology reviews : PER. 14(1)
In recent years more and more genetic defects along the GHRH-GH-IGF-I axis have been reported. Mutations of the IGF-I receptor (R) are a rare abnormality of whom only the heterozygote progenies survive.To summarize, from the literature, data on birth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b7e0e95befd87c74fc0cd68a049d3a6
https://pubmed.ncbi.nlm.nih.gov/28508613
https://pubmed.ncbi.nlm.nih.gov/28508613
Publikováno v:
Obesity Research & Clinical Practice. 8:e55-e62
To evaluate changes in adiposity in congenital GH/IGF-1 deficient children during hGH or IGF-1 treatment.27 children with congenital isolated growth hormone deficiency (cIGHD) treated with hGH for 2.5-15.2 years (mean 10.0 ± 3.4), 18 children wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2adc22065caf1c67ef86a53617b487c7
https://doi.org/10.1016/j.orcp.2012.11.001
https://doi.org/10.1016/j.orcp.2012.11.001
Publikováno v:
Journal of investigative medicine : the official publication of the American Federation for Clinical Research. 64(2)
The relationship between triglyceridemia and diabetes mellitus remains unclear. This study evaluated the risk of diabetes and impaired fasting glucose associated with a wide range of triglyceride levels. A longitudinal retrospective study was carried
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf99d780a9013977b4d208b773dd9291
https://pubmed.ncbi.nlm.nih.gov/26911628
https://pubmed.ncbi.nlm.nih.gov/26911628
Publikováno v:
Growth hormoneIGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society. 25(4)
To describe the growth, development and puberty in children with congenital IGHD before and during hGH treatment.Patients with cIGHD treated by hGH between the years 1958-1992.All patients were diagnosed, treated and followed in our clinic.Data were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6895fc874a5cc3b5f332c8d0beafff9a
https://pubmed.ncbi.nlm.nih.gov/26077773
https://pubmed.ncbi.nlm.nih.gov/26077773