Zobrazeno 1 - 10
of 800
pro vyhledávání: '"J. de Schepper"'
Autor:
M. Thomas, D. Beckers, C. Brachet, H. Dotremont, M.-C. Lebrethon, P. Lysy, G. Massa, N. Reynaert, R. Rooman, S. van der Straaten, M. Roelants, J. De Schepper
Publikováno v:
International Journal of Endocrinology, Vol 2018 (2018)
Objectives. Information on the efficacy of GH treatment in short SGA children starting their treatment in adolescence is limited. Therefore, adult height (AH), total height gain, and pubertal height gain were evaluated in short SGA children who start
Externí odkaz:
https://doaj.org/article/a22a6198c18743169b28d71373a6b4cf
Publikováno v:
International Journal of Endocrinology, Vol 2018 (2018)
Background. Intracytoplasmic sperm injection (ICSI) conception presents the early embryo with a radically different environment, which may lead to permanent alterations to key cardiometabolic processes. Blood pressure, indicators of insulin resistanc
Externí odkaz:
https://doaj.org/article/b739af6e511a46ae9aac47220a8077fe
Autor:
M Willems, C Olsen, B Caljon, Y Heremans, V Vloeberghs, J De schepper, H Tournaye, D Van Saen, E Goossens
Publikováno v:
Human Reproduction. 37
Study question Which genes are differentially expressed between patients with and without testicular fibrosis? Summary answer This study revealed three X-related genes MXRA5, DCX and VC3BX, which may be involved in Klinefelter-related testicular fibr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c341fd85a600ac0f113033cb873efe5
https://doi.org/10.1093/humrep/deac107.083
https://doi.org/10.1093/humrep/deac107.083
Publikováno v:
Tijdschrift voor psychiatrie. 63(6)
Prader-Willi syndrome (PWS) is a genetic syndrome characterized by dysmorphic features and endocrine, cognitive and psychiatric problems. Psychiatric problems interfere with the transition from pediatric to adult care. Psychiatric expertise is needed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec8a1daa71343c89250ad1b2f6c28f52
https://pubmed.ncbi.nlm.nih.gov/34231862
https://pubmed.ncbi.nlm.nih.gov/34231862
Autor:
Etienne Cavalier, Michaël R. Laurent, J. De Schepper, Jean-Marc Kaufman, Bruno Lapauw, Jean-Jacques Body, Evelien Gielen, Olivier Bruyère, Serge Rozenberg, Stefan Goemaere, Pierre Bergmann
Publikováno v:
Maturitas, 138
MATURITAS
MATURITAS
This narrative review discusses several aspects of the management of osteoporosis in patients under 50 years of age. Peak bone mass is genetically determined but can also be affected by lifestyle factors. Puberty constitutes a vulnerable period. Idio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2b5b7f000efa62df2e67c85061a0ba9
https://pubmed.ncbi.nlm.nih.gov/32631584
https://pubmed.ncbi.nlm.nih.gov/32631584
Akademický článek
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Akademický článek
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Autor:
Koen Huysentruyt, E. De Wachter, Yvan Vandenplas, J. De Schepper, Konstantinos Gerasimidis, Bruno Hauser, B Nichols
BACKGROUND: The measurement of handgrip force (HGF) is recommended by the combined ESPEN-ESPGHAN-ECFS guidelines on nutrition care in cystic fibrosis (CF) patients. This recommendation is however based on data in small groups of adult CF patients, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efb6125310734224a5b5f137346de38b
https://europepmc.org/articles/PMC6512541/
https://europepmc.org/articles/PMC6512541/
Akademický článek
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Autor:
Jaak Billen, Sammy Goemaere, Roger Bouillon, Tom Fiers, Dorien Baetens, An Desloovere, Martine Cools, Adam Raes, Dirk Vanderschueren, Ivo Jans, E. De Baere, J. De Schepper, JM Kaufman
Publikováno v:
Bone. 81:89-96
Background Bi-allelic CYP24A1 mutations can cause idiopathic infantile hypercalcemia (IIH), adult-onset nephrocalcinosis, and possibly bone metabolism disturbances. It is currently unclear if heterozygous carriers experience clinical problems or bioc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a2604a85724209879cf043c858f51f2
https://doi.org/10.1016/j.bone.2015.06.018
https://doi.org/10.1016/j.bone.2015.06.018