Phenotyping and outcome on contemporary management in a German cohort of patients with peripartum cardiomyopathy von Haghikia, A, Podewski, E, Libhaber, E, Labidi, S, Fischer, D, Roentgen, P, Tsikas, D, Jordan, J, Lichtinghagen, R, von Kaisenberg, C. S, Struman, Ingrid, Bovy, Nicolas, Sliwa, K, Bauersachs, J, Hilfiker-Kleiner, Denise

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Lymphatic vessel hypoplasia in fetuses with Turner syndrome von von Kaisenberg, C.S., Nicolaides, K.H., Brand-Saberi, B.

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Fetal parvovirus B19 infection von Von Kaisenberg, C. S., Jonat, W.

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First-trimester placental growth factor as a marker for hypertensive disorders and SGA von Cowans, N. J., Stamatopoulou, A., Matwejew, E., von Kaisenberg, C. S., Spencer, K.

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Glycosaminoglycans and proteoglycans in the skin of aneuploid fetuses with increased nuchal translucency von von Kaisenberg, C.S., Prols, F., Nicolaides, K.H., Maass, N., Meinhold‐Heerlein, I., Brand‐Saberi, B.

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Fetal transabdominal biometry at 11–14 weeks of gestation von Von Kaisenberg, C. S., Fritzer, E., Kühling, H., Jonat, W.

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Severe fetal brain damage subsequent to acute maternal hypoxemic deterioration in COVID‐19 von Düppers, A. L., Bohnhorst, B., Bültmann, E., Schulz, T., Higgins‐Wood, L., Kaisenberg, C. S.

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Hyaluronan in the nuchal skin of chromosomally abnormal fetuses von Böhlandt, S., von Kaisenberg, C.S., Wewetzer, K., Christ, B., Nicolaides, K.H., Brand-Saberi, B.

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Lymphatic capillary hypoplasia in the skin of fetuses with increased nuchal translucency and Turner's syndrome: comparison with trisomies and controls von von Kaisenberg, C.S., Wilting, J., Dörk, T., Nicolaides, K.H., Meinhold-Heerlein, I., Hillemanns, P., Brand-Saberi, B.

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Collagen type VI gene expression in the skin of trisomy 21 fetuses von Von Kaisenberg, C.S., Brand-Saberi, B., Christ, B., Vallian, S., Farzaneh, F., Nicolaides, K.H.

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Screening for trisomy 21 by fetal nuchal translucency and maternal age: a multicenter project in Germany, Austria and Switzerland von Gasiorek‐Wiens, A., Tercanli, S., Kozlowski, P., Kossakiewicz, A., Minderer, S., Meyberg, H., Kamin, G., Germer, U., Bielicki, M., Hackelöer, B. J., Sarlay, D., Kuhn, P., Klapp, J., Bahlmann, F., Pruggmayer, M., Schneider, K. T. M., Seefried, W., Fritzer, E., von Kaisenberg, C. S.

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Role of vitamin D in cell-cell interaction of fetal endothelial progenitor cells and umbilical cord endothelial cells in a preeclampsia-like model von Brodowski, L, Schröder-Heurich, B, Hubel, C A, Vu, T H, von Kaisenberg, C S, von Versen-Höynck, F

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Phenotypical variation in cousins with the identical partial trisomy 9 (pter‐q22.2) and 7 (q35‐qter) at 16 and 23 weeks gestation von Metzke‐Heidemann, S., Kuhling‐von Kaisenberg, H., Caliebe, A., Janssen, D., Jonat, W., Grote, W., von Kaisenberg, C.S.

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Cranial and cerebral signs in the diagnosis of spina bifida between 18 and 22 weeks of gestation: a German multicentre study von Bahlmann, F., Reinhard, I., Schramm, T., Geipel, A., Gembruch, U., von Kaisenberg, C. S., Schmitz, R., Stupin, J., Chaoui, R., Karl, K., Kalache, K., Faschingbauer, F., Ponnath, M., Rempen, A., Kozlowski, P.

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Maternal Serum ADAM-12 as a Potential Marker for Different Adverse Pregnancy Outcomes von Matwejew, E., Cowans, N.J., Stamatopoulou, A., Spencer, K., von Kaisenberg, C.S.

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A Case of Fetal Parvovirus B19 Myocarditis, Terminal Cardiac Heart Failure, and Perinatal Heart Transplantation von von Kaisenberg, C.S., Bender, G., Scheewe, J., Hirt, S.W., Lange, M., Stieh, J., Kramer, H.H., Jonat, W.

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A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset von Gasiorek-Wiens, A., Kotsis, S., Staboulidou, I., Stumm, M., Wegner, R. D., Soergel, P., Schippert, C., von Kaisenberg, C. S.

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Prox1 is a marker of ectodermal placodes, endodermal compartments, lymphatic endothelium and lymphangioblasts von Rodriguez-niedenführ, M, Papoutsi, M, Christ, B, Nicolaides, K H, von Kaisenberg, Cs, Tomarev, S I, Wilting, J

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The homeobox transcription factor Prox1 is highly conserved in embryonic hepatoblasts and in adult and transformed hepatocytes, but is absent from bile duct epithelium von Dudas, J, Papoutsi, M, Hecht, M, Elmaouhoub, A, Saile, B, Christ, B, Tomarev, S I, von Kaisenberg, C S, Schweigerer, L, Ramadori, G, Wilting, J

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Severe fetal growth restriction at 26–32 weeks: key messages from the TRUFFLE study von Bilardo, C. M., Hecher, K., Visser, G. H. A., Papageorghiou, A. T., Marlow, N., Thilaganathan, B., Van Wassenaer‐Leemhuis, A., Todros, T., Marsal, K., Frusca, T., Arabin, B., Brezinka, C., Derks, J. B., Diemert, A., Duvekot, J. J., Ferrazzi, E., Ganzevoort, W., Martinelli, P., Ostermayer, E., Schlembach, D., Valensise, H., Thornton, J., Wolf, H., Lees, C., Calda, P., Gordjin, S., Gyselaers, W., Klaritsch, P., Lobmaier, S., Manz, M., Napolitano, R., Prefumo, F., Schild, R., Stampalija, T., von Holsbeke, C., von Kaisenberg, C.

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