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Page 1
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.
Freud LR, Galloway S, Crowley TB, Moldenhauer J, Swillen A, Breckpot J, Borrell A, Vora NL, Cuneo B, Hoffman H, Gilbert L, Nowakowska B, Geremek M, Kutkowska-Kaźmierczak A, Vermeesch JR, Devriendt K, Busa T, Sigaudy S, Vigneswaran T, Simpson JM, Dungan J, Gotteiner N, Gloning KP, Digilio MC, Unolt M, Putotto C, Marino B, Repetto G, Fadic M, Garcia-Minaur S, Achón Buil A, Thomas MA, Fruitman D, Beecroft T, Hui PW, Oskarsdottir S, Bradshaw R, Criebaum A, Norton ME, Lee T, Geiger M, Dunnington L, Isaac J, Wilkins-Haug L, Hunter L, Izzi C, Toscano M, Ghi T, McGlynn J, Romana Grati F, Emanuel BS, Gaiser K, Gaynor JW, Goldmuntz E, McGinn DE, Schindewolf E, Tran O, Zackai EH, Yan Q, Bassett AS, Wapner R, McDonald-McGinn DM. Freud LR, et al. Among authors: gloning kp. Am J Obstet Gynecol. 2024 Mar;230(3):368.e1-368.e12. doi: 10.1016/j.ajog.2023.09.005. Epub 2023 Sep 16. Am J Obstet Gynecol. 2024. PMID: 37717890
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants.
Bedei I, Gehrke T, Gloning KP, Meyer-Wittkopf M, Willner D, Krapp M, Scharf A, Degenhardt J, Heling KS, Kozlowski P, Trautmann K, Jahns KM, Geipel A, Baumüller JE, Wilhelm L, Gottschalk I, Schröer A, Graf A, Wolter A, Schenk J, Weber A, Van den Veyver IB, Axt-Fliedner R. Bedei I, et al. Among authors: gloning kp. Prenat Diagn. 2023 Feb;43(2):192-206. doi: 10.1002/pd.6320. Epub 2023 Feb 9. Prenat Diagn. 2023. PMID: 36726284
Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcome.
Bedei I, Gloning KP, Joyeux L, Meyer-Wittkopf M, Willner D, Krapp M, Scharf A, Degenhardt J, Heling KS, Kozlowski P, Trautmann K, Jahns KM, Geipel A, Tekesin I, Elsässer M, Wilhelm L, Gottschalk I, Baumüller JE, Birdir C, Schröer A, Zöllner F, Wolter A, Schenk J, Gehrke T, Spaeth A, Axt-Fliedner R. Bedei I, et al. Among authors: gloning kp. Prenat Diagn. 2023 Feb;43(2):183-191. doi: 10.1002/pd.6302. Epub 2023 Jan 31. Prenat Diagn. 2023. PMID: 36600414
Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?
Bedei IA, Graf A, Gloning KP, Meyer-Wittkopf M, Willner D, Krapp M, Hentze S, Scharf A, Degenhardt J, Heling KS, Kozlowski P, Trautmann K, Jahns K, Geipel A, Tekesin I, Elsässer M, Wilhelm L, Gottschalk I, Baumüller JE, Birdir C, Zöllner F, Wolter A, Schenk J, Gehrke T, Keil C, Espinosa J, Axt-Fliedner R. Bedei IA, et al. Among authors: gloning kp. J Clin Med. 2022 Aug 5;11(15):4588. doi: 10.3390/jcm11154588. J Clin Med. 2022. PMID: 35956203 Free PMC article.
Postponing Early intrauterine Transfusion with Intravenous immunoglobulin Treatment; the PETIT study on severe hemolytic disease of the fetus and newborn.
Zwiers C, van der Bom JG, van Kamp IL, van Geloven N, Lopriore E, Smoleniec J, Devlieger R, Sim PE, Ledingham MA, Tiblad E, Moise KJ Jr, Gloning KP, Kilby MD, Overton TG, Jørgensen DS, Schou KV, Paek B, Walker M, Parry E, Oepkes D, de Haas M. Zwiers C, et al. Among authors: gloning kp. Am J Obstet Gynecol. 2018 Sep;219(3):291.e1-291.e9. doi: 10.1016/j.ajog.2018.06.007. Epub 2018 Jun 11. Am J Obstet Gynecol. 2018. PMID: 29902448
Thymus Growth and Fetal Immune Responses in Diabetic Pregnancies.
Warncke K, Lickert R, Eitel S, Gloning KP, Bonifacio E, Sedlmeier EM, Becker P, Knoop J, Beyerlein A, Ziegler AG. Warncke K, et al. Among authors: gloning kp. Horm Metab Res. 2017 Nov;49(11):892-898. doi: 10.1055/s-0043-120671. Epub 2017 Nov 14. Horm Metab Res. 2017. PMID: 29136677
Prenatal sonographic diagnosis of skeletal dysplasias.
Schramm T, Gloning KP, Minderer S, Daumer-Haas C, Hörtnagel K, Nerlich A, Tutschek B. Schramm T, et al. Among authors: gloning kp. Ultrasound Obstet Gynecol. 2009 Aug;34(2):160-70. doi: 10.1002/uog.6359. Ultrasound Obstet Gynecol. 2009. PMID: 19548204 Free article.
43 results