Zobrazeno 1 - 10
of 142
pro vyhledávání: '"N Yordam"'
Publikováno v:
European Journal of Endocrinology. 131:504-508
Hatun Ş, Yordam N, Çalikoǧlu AS. Serum 3α-androstandiol glucuronide measurements in children with congenital adrenal hyperplasia. Eur J Endocrinol 1994;131:504–8. ISSN 0804–4643 To determine the value of 3α-androstanediol glucuronide (3-AG)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc163e407d7f9f094b4929039d795326
https://doi.org/10.1530/eje.0.1310504
https://doi.org/10.1530/eje.0.1310504
Publikováno v:
Pediatric endocrinology reviews : PER. 1
Newborn screening for congenital hypothyroidism (CH) is one of the major achievements of preventive medicine, as the condition occurs frequently (1/4000 newborns) and results in brain damage if not detected and treated in the first few days of life.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::45844527c38393a7bd0933416e02c886
https://pubmed.ncbi.nlm.nih.gov/16444156
https://pubmed.ncbi.nlm.nih.gov/16444156
Autor:
Katherine J. Borthwick, Uwe Kornak, Fiona E. Karet, Seza Ozen, Aysin Bakkaloglu, N Yordam, N Kandemir, G N Shah, Rezan Topaloglu, H Mocan, W S Sly
The rare bone thickening disease osteopetrosis occurs in various forms, one of which is accompanied by renal tubular acidosis (RTA), and is known as Guibaud-Vainsel syndrome or marble brain disease. Clinical manifestations of this autosomal recessive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff1ebf1dc8d0b0fee24f75355b1e3788
http://hdl.handle.net/11655/14234
http://hdl.handle.net/11655/14234
Publikováno v:
Hormone research. 56(1-2)
To show the importance of priming prior to growth hormone (GH) stimulation tests in the diagnosis of GH deficiency, the effect of different doses and schedules of testosterone (T) on GH levels.Eighty-four prepubertal and early pubertal boys whose hei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98d4cf7bdb07939a1aec4f873eea5c63
https://pubmed.ncbi.nlm.nih.gov/12324717
https://pubmed.ncbi.nlm.nih.gov/12324717
Autor:
N, Kandemir, N, Yordam
Publikováno v:
The Turkish journal of pediatrics. 43(4)
It is a general belief that early and adequate thyroid hormone replacement achieves normalization of growth as well as disappearance of clinical sings and symptoms of hypothyroidism. Due to the lack of comprehensive growth studies, height prognosis h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::624e85f7032b3f2230e10b617c95b879
https://pubmed.ncbi.nlm.nih.gov/11765159
https://pubmed.ncbi.nlm.nih.gov/11765159
Autor:
G. Gilli, U. Heinrich, D.A. Price, S.J. Rose, R.G. Rosenfeld, Christine P Burren, Maryam Razzaghy-Azar, A. Al-Ashwal, P Rochiccioli, M B Ranke, M.A. Preece, Katie A. Woods, P.G. Chatelain, N. Yordam, M. Tauber, Martin O. Savage, P.A. Crock
Publikováno v:
Hormone research. 55(3)
Objective: Classical growth hormone insensitivity syndrome (GHIS) comprises a dysmorphic phenotype, extreme short stature (height SDS < 3), normal GH and low IGF-I and IGFBP-3. Wide clinical variation is recognised with classical and atypical forms.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c6065daa1401a8dac3c8046cad9e0a5
https://pubmed.ncbi.nlm.nih.gov/11549873
https://pubmed.ncbi.nlm.nih.gov/11549873
Publikováno v:
The Turkish journal of pediatrics. 40(3)
In this study the presence of pituitary-hypothalamic abnormalities was searched by magnetic resonance (MR) imaging in 30 children (18 males and 12 females, aged 7.4 to 23 years) with isolated growth hormone deficiency (IGHD). Small anterior pituitary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5f4f8190d5c40cd610fee7fa82ca3617
https://pubmed.ncbi.nlm.nih.gov/9763902
https://pubmed.ncbi.nlm.nih.gov/9763902
Publikováno v:
The Turkish journal of pediatrics. 40(1)
From a total of 118 patients treated for growth hormone deficiency, 37 (23 boys, 14 girls) have reached their final height. Twenty-five patients had isolated growth hormone deficiency (IGHD) and 12 had multiple pituitary hormone deficiency (MPHD). Gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ae766ff0a12f62076430d8e609f688de
https://pubmed.ncbi.nlm.nih.gov/9673529
https://pubmed.ncbi.nlm.nih.gov/9673529
Publikováno v:
The Turkish journal of pediatrics. 39(3)
We report two cases of Leprechaunism with the classical features. The first case had hyperglycemia and severe hyperinsulinemia. The postmortem examination of the second child revealed enlargement of both ovaries, islet cell hyperplasia in the pancrea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf6e8eb188080781364e3011f340a122
https://pubmed.ncbi.nlm.nih.gov/9339119
https://pubmed.ncbi.nlm.nih.gov/9339119
Publikováno v:
The Journal of clinical endocrinology and metabolism. 82(2)
The GH receptor (GHR) is a member of the cytokine receptor superfamily; GH binding protein is the solubilized extracellular domain of the GHR. Abnormalities in the GHR produce an autosomal recessive form of GH resistance, the Laron syndrome, characte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::608fd4dce553a2e05d04e940cba82397
https://pubmed.ncbi.nlm.nih.gov/9024232
https://pubmed.ncbi.nlm.nih.gov/9024232