Zobrazeno 1 - 10
of 122
pro vyhledávání: '"H H, Bode"'
Autor:
M. S. A. Kumar, A. R. Gwosdow, J. A. Spencer, N. A. O'Connell, Abdul B. Abou-Samra, H. H. Bode, R. K. Agarwal
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 263:E461-E466
Interleukin-1 (IL-1) has been shown to stimulate corticosterone release from the adrenal gland directly, and indirectly through activation of the hypothalamic-pituitary-adrenal axis. The aim of this paper was to determine whether IL-1-stimulated cort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb42752520aa417ee4297fede8eec212
https://doi.org/10.1152/ajpendo.1992.263.3.e461
https://doi.org/10.1152/ajpendo.1992.263.3.e461
Autor:
A L, Boehmer, A O, Brinkmann, L A, Sandkuijl, D J, Halley, M F, Niermeijer, S, Andersson, F H, de Jong, H, Kayserili, M A, de Vroede, B J, Otten, C W, Rouwé, B B, Mendonça, C, Rodrigues, H H, Bode, P E, de Ruiter, H A, Delemarre-van de Waal, S L, Drop
Publikováno v:
The Journal of clinical endocrinology and metabolism. 84(12)
17Beta-hydroxysteroid dehydrogenase-3 (17betaHSD3) deficiency is an autosomal recessive form of male pseudohermaphroditism caused by mutations in the HSD17B3 gene. In a nationwide study on male pseudohermaphroditism among all pediatric endocrinologis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96f4284f72aa41dd4ad0a211c7d1058b
https://pubmed.ncbi.nlm.nih.gov/10599740
https://pubmed.ncbi.nlm.nih.gov/10599740
Publikováno v:
American journal of medical genetics. 83(1)
Males with X-linked Kallmann syndrome (XLKS) may have renal agenesis. We studied a large kindred with a history of eight males affected by XLKS born in five generations. Their XLKS was shown to be due to an intragenic mutation of the KAL-1 gene. We a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1829537c1f63675274d74e880ea2e121
https://pubmed.ncbi.nlm.nih.gov/10076881
https://pubmed.ncbi.nlm.nih.gov/10076881
Publikováno v:
The Journal of pediatrics. 134(2)
The purpose of this study was to evaluate the usefulness of 17 hydroxyprogesterone (17OHP) determination in dried filter paper blood samples from patients with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency. It was hypothesized th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::79eef3aff1396e74e21f8a16c65a077a
https://pubmed.ncbi.nlm.nih.gov/9931518
https://pubmed.ncbi.nlm.nih.gov/9931518
Publikováno v:
Pediatric research. 28(5)
The hypothalamic-pituitary-ovarian hormone secretion patterns were evaluated in two women with 45,X Turner syndrome, spontaneous sexual development, and monthly menstrual periods. Each women had serum gonadotropin and sex steroid determinations durin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ea42fa13053fd88c744fb7b2d91a60b
https://pubmed.ncbi.nlm.nih.gov/2255575
https://pubmed.ncbi.nlm.nih.gov/2255575
Publikováno v:
The American journal of physiology. 258(1 Pt 1)
The effect of varying doses of purified human interleukin 1 (IL-1) on rectal temperature (Tr), hypothalamic corticotropin-releasing hormone (CRH), pituitary and plasma adrenocorticotropic hormone (ACTH), and plamsa corticosterone was examined in inta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9937a0f9378be606bab809a97bba2838
https://pubmed.ncbi.nlm.nih.gov/2154118
https://pubmed.ncbi.nlm.nih.gov/2154118
Autor:
Anthony Walker, M Irama, D S Peat, J Senkungu, Richard J M Coward, J Axton, Peter W. Mathieson, D Nansera, J Ellis, H H Bode
Publikováno v:
Kidney International. (6):569-573
Acute renal disease is common in sub-Saharan Africa, with high mortality. Its etiology is poorly understood; quartan malaria owing to Plasmodium malariae was implicated in previous series. Few previous studies have included histological data; further
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e51e729c555553be583c6cbcef3f5a
Publikováno v:
Infusionstherapie und klinische Ernahrung. Sonderheft. 3
The jejunoileal bypass is, of all the current therapeutic possibilities, the only permanent method for the successful treatment of a patient with hypothalamic obesity. Pre-operatively, it is advisable, however, to reduce the body weight by exclusive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46247bc97fda43c0ea5dff5253696aef
https://pubmed.ncbi.nlm.nih.gov/1078530
https://pubmed.ncbi.nlm.nih.gov/1078530
Publikováno v:
The New England journal of medicine. 318(10)
It has been suggested that complete catch-up growth is achieved with treatment in patients with juvenile acquired hypothyroidism. We tested this assumption by examining long-term growth in 18 girls (mean [+/- SD] age, 11.4 +/- 2.7 years; bone age, 6.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e4db5b0c87df8dd63ccfb50ab1c7638c
https://pubmed.ncbi.nlm.nih.gov/3344006
https://pubmed.ncbi.nlm.nih.gov/3344006