Zobrazeno 1 - 10
of 206
pro vyhledávání: '"Adeline K"'
Autor:
Eve Stern, Nadia Schoenmakers, Adeline K. Nicholas, Eran Kassif, Orit Pinhas Hamiel, Yonatan Yeshayahu
Publikováno v:
JCRPE, Vol 14, Iss 2, Pp 221-226 (2022)
Congenital hypothyroidism (CH) due to dyshormonogenesis may occur due to mutations in any of the key genes involved in thyroid hormone biosynthesis (TG, TPO, DUOX2, DUOXA2, SLC5A5, IYD, SLC26A4 and SLC26A7). Mutations in the thyroglobulin gene (TG) a
Externí odkaz:
https://doaj.org/article/a5779d85baa3427090de90f840d39211
Publikováno v:
Heliyon, Vol 9, Iss 2, Pp e13689- (2023)
The antidiabetic effects of the methanol extract of the stem bark of Ceiba pentandra (Cp) have been demonstrated in various experimental models. Besides, this extract is rich in 8-formyl-7-hydroxy-5-isopropyl-2-methoxy-3-methyl-1,4-naphthaquinone, 2,
Externí odkaz:
https://doaj.org/article/9d01bd78c7604e52892152168c5c1417
Autor:
Aslam Shiraz, Nagayasu Egawa, Daniël M. Pelt, Robin Crawford, Adeline K. Nicholas, Veronika Romashova, Peter Sasieni, Heather Griffin, John Doorbar
Publikováno v:
EBioMedicine, Vol 82, Iss , Pp 104157- (2022)
Summary: Background: Primary HPV screening, due to its low specificity, requires an additional liquid-based cytology (LBC) triage test. However, even with LBC triage there has been a near doubling in the number of patients referred for colposcopy in
Externí odkaz:
https://doaj.org/article/d0730386696d4a3ea2475e99548ec729
Autor:
Nikolina Zdraveska, Mirjana Kocova, Adeline K. Nicholas, Violeta Anastasovska, Nadia Schoenmakers
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Neonatal screening in Macedonia detects congenital hypothyroidism (CH) with an incidence of 1 in 1,585, and more than 50% of cases exhibit a normally located gland-in-situ (GIS). Monogenic mutations causing dyshormonogenesis may underlie GIS CH; addi
Externí odkaz:
https://doaj.org/article/39695879f4994480b45cb39e822b7ee6
Autor:
Briottet, X., Adeline, K., Bajjouk, T., Carrère, V., Chami, M., Constans, Y., Derimian, Y., Dupiau, A., Dumont, M., Doz, S., Fabre, S., Foucher, P.Y., Herbin, H., Jacquemoud, S., Lang, M., Le Bris, A., Litvinov, P., Loyer, S., Marion, R., Minghelli, A., Miraglio, T., Sheeren, D., Szymanski, B., Romand, F., Desjardins, C., Rodat, D., Cheul, B.
Publikováno v:
In ISPRS Open Journal of Photogrammetry and Remote Sensing April 2024 12
Autor:
Wuyt, Adeline K., Nguelefack-Mbuyo, Elvine P., Fofié, Christian K., Nguelefack, Télesphore B.
Publikováno v:
In Heliyon February 2023 9(2)
Autor:
Gomez, C., Adeline, K., Bacha, S., Driessen, B., Gorretta, N., Lagacherie, P., Roger, J.M., Briottet, X.
Publikováno v:
In Remote Sensing of Environment January 2018 204:18-30
Autor:
Bacchelli, Chiara, Moretti, Federico A., Carmo, Marlene, Adams, Stuart, Stanescu, Horia C., Pearce, Kerra, Madkaikar, Manisha, Gilmour, Kimberly C., Nicholas, Adeline K., Woods, C. Geoffrey, Kleta, Robert, Beales, Phil L., Qasim, Waseem, Gaspar, H. Bobby
Publikováno v:
In The Journal of Allergy and Clinical Immunology February 2017 139(2):634-642
Autor:
Wuyt, Adeline K.1, Nankam, Pamela A. Nono2, Nguelefack-Mbuyo, Elvine P.1, Nguelefack, Télesphore B.1 nguelefack@yahoo.fr
Publikováno v:
Cameroon Journal of Experimental Biology. 2022, Vol. 16 Issue 1, p76-79. 4p.
Autor:
Adeline K Nicholas, Eran Kassif, Nadia Schoenmakers, Orit Pinhas Hamiel, Eve Stern, Yonatan Yeshayahu
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 14:221-226
Congenital Hypothyroidism (CH) due to dyshormonogenesis may occur due to mutations in any of the key genes involved in thyroid hormone biosynthesis (TG, TPO, DUOX2, DUOXA2, SLC5A5, IYD, SLC26A4 and SLC26A7). Mutations in the Thyroglobulin gene (TG) a