Bedei IA - Search Results

1

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. J Clin Med. 2022 Aug 5;11(15):4588. doi: 10.3390/jcm11154588. J Clin Med. 2022. PMID: 35956203 Free PMC article.

2

First-trimester screening for trisomy 21 with adjustment for biochemical results of previous pregnancies.

Wright D, Syngelaki A, Birdir C, Bedei I, Nicolaides KH. Wright D, et al. Fetal Diagn Ther. 2011;30(3):194-202. doi: 10.1159/000328710. Epub 2011 Jun 25. Fetal Diagn Ther. 2011. PMID: 21709403

3

Natural history of pulmonary atresia with intact ventricular septum (PAIVS) and critical pulmonary stenosis (CPS) and prediction of outcome.

Wolter A, Markert N, Wolter JS, Kurkevych A, Degenhardt J, Ritgen J, Stressig R, Enzensberger C, Bedei I, Vorisek C, Schenk J, Graupner O, Khalil M, Thul J, Jux C, Axt-Fliedner R. Wolter A, et al. Arch Gynecol Obstet. 2021 Jul;304(1):81-90. doi: 10.1007/s00404-020-05929-0. Epub 2021 Feb 14. Arch Gynecol Obstet. 2021. PMID: 33585987 Free PMC article.

4

Chances and Challenges of New Genetic Screening Technologies (NIPT) in Prenatal Medicine from a Clinical Perspective: A Narrative Review.

Bedei I, Wolter A, Weber A, Signore F, Axt-Fliedner R. Bedei I, et al. Genes (Basel). 2021 Mar 29;12(4):501. doi: 10.3390/genes12040501. Genes (Basel). 2021. PMID: 33805390 Free PMC article. Review.

5

Fetal therapy of LUTO (lower urinary tract obstruction) - a follow-up observational study.

Keil C, Bedei I, Sommer L, Koemhoff M, Axt-Fliedner R, Köhler S, Weber S. Keil C, et al. J Matern Fetal Neonatal Med. 2022 Dec;35(25):8536-8543. doi: 10.1080/14767058.2021.1988562. Epub 2021 Oct 15. J Matern Fetal Neonatal Med. 2022. PMID: 34652254 Free article.

6

Analysis of the Results of Sonographic Screening Examinations According to the Maternity Guidelines Before and After the Introduction of the Extended Basic Screening (IIb Screening) in Hesse.

Schmand C, Misselwitz B, Hudel H, Bedei I, Wolter A, Schenk J, Keil C, Köhler S, Axt-Fliedner R. Schmand C, et al. Ultraschall Med. 2023 Aug;44(4):e175-e183. doi: 10.1055/a-1778-3585. Epub 2022 Mar 18. Ultraschall Med. 2023. PMID: 35304733 English.

7

Congenital hip dysplasia after open fetoscopic repair for open spina bifida.

Keil C, Bedei I, Belfort M, Köhler S, Sanz Cortes M, Axt-Fliedner R, Espinoza J. Keil C, et al. Ultrasound Obstet Gynecol. 2023 Jan;61(1):118. doi: 10.1002/uog.26069. Ultrasound Obstet Gynecol. 2023. PMID: 36099428 Free article. No abstract available.

8

The Evolution and Developing Importance of Fetal Magnetic Resonance Imaging in the Diagnosis of Congenital Cardiac Anomalies: A Systematic Review.

Mamalis M, Bedei I, Schoennagel B, Kording F, Reitz JG, Wolter A, Schenk J, Axt-Fliedner R. Mamalis M, et al. J Clin Med. 2022 Nov 28;11(23):7027. doi: 10.3390/jcm11237027. J Clin Med. 2022. PMID: 36498602 Free PMC article. Review.

9

The Value of Delta Middle Cerebral Artery Peak Systolic Velocity for the Prediction of Twin Anemia-Polycythemia Sequence-Analysis of a Heterogenous Cohort of Monochorionic Twins.

de Sainte Fare A, Bedei I, Wolter A, Schenk J, Widriani E, Keil C, Koehler S, Bahlmann F, Strizek B, Gembruch U, Berg C, Axt-Fliedner R. de Sainte Fare A, et al. J Clin Med. 2022 Dec 19;11(24):7541. doi: 10.3390/jcm11247541. J Clin Med. 2022. PMID: 36556157 Free PMC article.

10

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. Prenat Diagn. 2023 Feb;43(2):183-191. doi: 10.1002/pd.6302. Epub 2023 Jan 31. Prenat Diagn. 2023. PMID: 36600414

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