Zobrazeno 1 - 10
of 166
pro vyhledávání: '"W. Sorgo"'
Publikováno v:
International Journal of Obesity. 31:1509-1519
To investigate clinical and laboratory markers of pubertal development in a large sample of obese children and adolescents.Analysis of parameters of sexual maturation in 1232 obese individuals (582 boys) aged 6-18 years (mean 13.0+/-2.42 years). Clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d8f985d5d97b656f1ecc40cda1e22e8
https://doi.org/10.1038/sj.ijo.0803691
https://doi.org/10.1038/sj.ijo.0803691
Autor:
Martin Wabitsch, Josef Högel, Stefan A. Wudy, Eberhard Heinze, J. Homoki, Marlene Bleicher, W. Sorgo
Publikováno v:
Hormone Research in Paediatrics. 58:229-232
Objective: To investigate the possible contribution of plasma cortisol and growth hormone (GH) as reflected by insulin-like growth factor-I (IGF-I)/insulin-like growth factor-binding protein-3 (IGFBP-3) on insulin action in short-statured children. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6a5353c6439d47e708e587e4b9089a7
https://doi.org/10.1159/000066266
https://doi.org/10.1159/000066266
Publikováno v:
Acta neurochirurgica. 1(2-3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93f0d388ced9f6dd172639da474b48d7
https://pubmed.ncbi.nlm.nih.gov/24539094
https://pubmed.ncbi.nlm.nih.gov/24539094
Publikováno v:
Hormone Research in Paediatrics. 51:20-24
Excess secretion of growth hormone is a rare diagnosis in children or adolescents with tall stature. An oral glucose tolerance test (OGT) with determination of growth hormone is generally recommended to exclude this disorder. In order to test the val
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86a830b1c6dd83bd5fad688595f69fd2
https://doi.org/10.1159/000023308
https://doi.org/10.1159/000023308
Publikováno v:
Diabetologia. 41:542-547
Overweight in insulin-dependent diabetes mellitus (IDDM) has been repeatedly reported, especially in girls during adolescence. Potential pathophysiologic factors include tight metabolic control, insulin dose, treatment regimen, puberty and genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9892a301f7872c26541e360c120ea332
https://doi.org/10.1007/s001250050944
https://doi.org/10.1007/s001250050944
Publikováno v:
Monatsschrift Kinderheilkunde. 145:249-254
Fragestellung: Das gehaufte Auftreten eines Diabetes bei Wachstumshormonuberproduktion (Akromegalie, hypophysarer Gigantismus) ist lange bekannt. Methode: Im oralen Glukosetoleranztest (OGT) wurden Blutzucker und Insulin alle 30 min bestimmt. Zwei Pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f672cd2952cb56dc5923a5d1e1983856
https://doi.org/10.1007/s001120050123
https://doi.org/10.1007/s001120050123
Publikováno v:
Monatsschrift Kinderheilkunde. 145:230-234
Das Syndrom der persistierenden Muller-Strukturen (SPMS) ist definiert durch den Nachweis von Muller-Strukturen (Tuben, Uterus, proximale Vagina) bei Patienten mit vollstandig mannlich differenziertem auseren Genitale und normalem, mannlichen Chromos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5efaf47fa07e6d325ad273472a7b802
https://doi.org/10.1007/s001120050119
https://doi.org/10.1007/s001120050119
Autor:
Klaus-Peter Günther, Walther Vogel, W. Sorgo, Walter M. Teller, Rolf E. Brenner, Eberhard Heinze, Ingo Kennerknecht, Walter Just, Volker Schneider, A. Wolf, Gotthold Barbi, Petra von Saurma
Publikováno v:
American Journal of Medical Genetics. 59:62-67
We report on 12- and 14-year-old sisters with a 46,XY chromosome constitution, normal female external genitalia, and absence of gonadal tissue. Except for omphalocele, right renal agenesis and malrotation of the colon in the elder sister, the interna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8b9f06adee8fc2586c5a89bad9c0d20
https://doi.org/10.1002/ajmg.1320590114
https://doi.org/10.1002/ajmg.1320590114
Autor:
Ingo Kennerknecht, Renate Oberhoffer, Torsten Mattfeldt, Walther Vogel, W. Sorgo, Giovanni Negri, Walter M. Teller
Publikováno v:
American Journal of Medical Genetics. 47:1166-1170
We report on 2 phenotypic sisters, one with 46,XY; the other with 46,XX. The 2 girls had similar related internal malformations, including agonadism, hypoplasia of the right pulmonary artery, hypoplasia of the right lung, isolated dextrocardia with c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::014e83a80a8308e94b51dfa1e3fca521
https://doi.org/10.1002/ajmg.1320470807
https://doi.org/10.1002/ajmg.1320470807
Autor:
R. J. Jäger, L. Gortner, B. Heymer, W. Sorgo, M. Graf, R. Oberhoffer, Peter Bartmann, Milo Zachmann, H.P. Streb, U. Lattermann, Cecilia Ebensperger, Walter M. Teller
Publikováno v:
Hormone Research. 35:124-131
A full-term 46,XY female newborn presented with respiratory failure due to a right-sided diaphragmatic hernia. During surgical repair, exploration revealed isolated dextrocardia and hypoplasia of the right lung. Neither gonads nor wolffian or müller
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e72d9c50da9ff19687239b1397a0fe36
https://doi.org/10.1159/000181887
https://doi.org/10.1159/000181887