Works matching Fetal growth disorders


Results: 1019
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    Neurodevelopment at 2 years and umbilical artery Doppler in cases of very preterm birth after prenatal hypertensive disorder or suspected fetal growth restriction: EPIPAGE-2 prospective population-based cohort study.

    Published in:
    2020
    By:
    • Delorme, P.;
    • Kayem, G.;
    • Lorthe, E.;
    • Sentilhes, L.;
    • Zeitlin, J.;
    • Subtil, D.;
    • Rozé, J. C.;
    • Vayssière, C.;
    • Durox, M.;
    • Ancel, P. Y.;
    • Pierrat, V.;
    • Goffinet, F.;
    • Arnaud, Catherine;
    • Blanc, Julie;
    • Boileau, Pascal;
    • Debillon, Thierry;
    • D'Ercole, Claude;
    • Desplanches, Thomas;
    • Diguisto, Caroline;
    • Foix‐L'Hélias, Laurence
    Publication type:
    journal article
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    Is There a Correlation between Apelin and Insulin Concentrations in Early Second Trimester Amniotic Fluid with Fetal Growth Disorders?

    Published in:
    Journal of Clinical Medicine, 2023, v. 12, n. 9, p. 3166, doi. 10.3390/jcm12093166
    By:
    • Vrachnis, Dionysios;
    • Antonakopoulos, Nikolaos;
    • Fotiou, Alexandros;
    • Pergialiotis, Vasilios;
    • Loukas, Nikolaos;
    • Valsamakis, Georgios;
    • Iavazzo, Christos;
    • Stavros, Sofoklis;
    • Maroudias, Georgios;
    • Panagopoulos, Periklis;
    • Vlahos, Nikolaos;
    • Peppa, Melpomeni;
    • Stefos, Theodoros;
    • Mastorakos, George
    Publication type:
    Article
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    Maternal plasma syndecan-1: a biomarker for fetal growth restriction.

    Published in:
    Journal of Maternal-Fetal & Neonatal Medicine, 2023, v. 36, n. 1, p. 1, doi. 10.1080/14767058.2022.2150074
    By:
    • Juusela, Alexander;
    • Jung, Eunjung;
    • Gallo, Dahiana M.;
    • Bosco, Mariachiara;
    • Suksai, Manaphat;
    • Diaz-Primera, Ramiro;
    • Tarca, Adi L.;
    • Than, Nandor Gabor;
    • Gotsch, Francesca;
    • Romero, Roberto;
    • Chaiworapongsa, Tinnakorn
    Publication type:
    Article
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    Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 24, p. 4724, doi. 10.1093/hmg/ddp435
    By:
    • Azzi, Salah;
    • Rossignol, Sylvie;
    • Steunou, Virginie;
    • Sas, Theo;
    • Thibaud, Nathalie;
    • Danton, Fabienne;
    • Le Jule, Maryline;
    • Heinrichs, Claudine;
    • Cabrol, Sylvie;
    • Gicquel, Christine;
    • Le Bouc, Yves;
    • Netchine, Irene
    Publication type:
    Article
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