Search Results - "von Kaisenberg, C S"

Phenotyping and outcome on contemporary management in a German cohort of patients with peripartum cardiomyopathy by 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

“…Peripartum cardiomyopathy (PPCM) is a life-threatening heart disease developing towards the end of pregnancy or in the months following delivery in previously…”
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Lymphatic vessel hypoplasia in fetuses with Turner syndrome by von Kaisenberg, C.S., Nicolaides, K.H., Brand-Saberi, B.

“…Turner syndrome is associated with subcutaneous accumulation of fluid in the neck region that can be visualized sonographically from 10–14 weeks of gestation…”
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Fetal parvovirus B19 infection by Von Kaisenberg, C. S., Jonat, W.

“…Parvovirus B19 infection during pregnancy causes up to 27% cases of non‐immune hydrops in anatomically normal fetuses. The virus is believed to cause arrest of…”
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Fetal transabdominal biometry at 11–14 weeks of gestation by Von Kaisenberg, C. S., Fritzer, E., Kühling, H., Jonat, W.

“…Objective To establish comprehensive transabdominal ultrasonographic reference ranges for viable normal singleton human fetuses at 11–14 weeks' gestation…”
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First-trimester placental growth factor as a marker for hypertensive disorders and SGA by Cowans, N. J., Stamatopoulou, A., Matwejew, E., von Kaisenberg, C. S., Spencer, K.

“…Objective The objective of this study was to examine first‐trimester maternal serum placental growth factor (PlGF) levels in pregnancies which later develop…”
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Glycosaminoglycans and proteoglycans in the skin of aneuploid fetuses with increased nuchal translucency by von Kaisenberg, C.S., Prols, F., Nicolaides, K.H., Maass, N., Meinhold‐Heerlein, I., Brand‐Saberi, B.

“…BACKGROUND: First trimester increased fetal nuchal translucency is associated with fetal aneuploidies. One of the mechanisms of pathophysiology could be an…”
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Hyaluronan in the nuchal skin of chromosomally abnormal fetuses by Böhlandt, S., von Kaisenberg, C.S., Wewetzer, K., Christ, B., Nicolaides, K.H., Brand-Saberi, B.

“…Nuchal skin oedema at 10–14 weeks gestation, observed by ultrasonography as increased nuchal translucency (NT), is found in ~70% of fetuses with trisomies 21,…”
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Screening for trisomy 21 by fetal nuchal translucency and maternal age: a multicenter project in Germany, Austria and Switzerland by 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.

“…Objective To examine the effectiveness of screening for trisomy 21 by a combination of maternal age and fetal nuchal translucency thickness at 10–14 weeks of…”
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Collagen type VI gene expression in the skin of trisomy 21 fetuses by Von Kaisenberg, C.S., Brand-Saberi, B., Christ, B., Vallian, S., Farzaneh, F., Nicolaides, K.H.

“…Objective: To determine whether the mechanism for the retention of interstitial fluid in trisomy 21 fetuses presenting with nuchal translucency at 10–14 weeks'…”
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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 by von Kaisenberg, C.S., Wilting, J., Dörk, T., Nicolaides, K.H., Meinhold-Heerlein, I., Hillemanns, P., Brand-Saberi, B.

“…Fetuses with Turner's syndrome or trisomies 21, 18 and 13 show excess of skin, which can be visualized by ultrasonography as increased nuchal translucency at…”
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Severe fetal brain damage subsequent to acute maternal hypoxemic deterioration in COVID‐19 by Düppers, A. L., Bohnhorst, B., Bültmann, E., Schulz, T., Higgins‐Wood, L., Kaisenberg, C. S.

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A case of fetal parvovirus B19 myocarditis, terminal cardiac heart failure, and perinatal heart transplantation by von Kaisenberg, C S, Bender, G, Scheewe, J, Hirt, S W, Lange, M, Stieh, J, Kramer, H H, Jonat, W

“…We report a case of fetal cardiomegaly secondary to myocarditis as a result of intrauterine parvovirus B19 infection. The fetus was delivered through caesarean…”
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A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset by Gasiorek-Wiens, A., Kotsis, S., Staboulidou, I., Stumm, M., Wegner, R. D., Soergel, P., Schippert, C., von Kaisenberg, C. S.

“…Objective (1) To validate the mixture model in a single operator dataset and (2) to compare the detection rates for fetal chromosomal defects obtained from the…”
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Maternal serum ADAM-12 as a potential marker for different adverse pregnancy outcomes by Matwejew, E, Cowans, N J, Stamatopoulou, A, Spencer, K, von Kaisenberg, C S

“…To investigate first-trimester ADAM-12 levels in pregnancies which later develop hypertensive and growth complications. First-trimester serum samples (11(+0)…”
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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 by Metzke‐Heidemann, S., Kuhling‐von Kaisenberg, H., Caliebe, A., Janssen, D., Jonat, W., Grote, W., von Kaisenberg, C.S.

“…From the study of numerical and structural chromosomal abnormalities, there is convincing evidence and accumulating information of a direct karyotype to…”
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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 by Brodowski, L, Schröder-Heurich, B, Hubel, C A, Vu, T H, von Kaisenberg, C S, von Versen-Höynck, F

“…Maternal endothelial dysfunction is a cental feature of preeclampsia (PE), a hypertensive disorder of pregnancy. Factors in the maternal circulation are…”
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Prox1 is a marker of ectodermal placodes, endodermal compartments, lymphatic endothelium and lymphangioblasts by Rodriguez-Niedenführ, M, Papoutsi, M, Christ, B, Nicolaides, K H, von Kaisenberg, C S, Tomarev, S I, Wilting, J

“…The lymphatic endothelium has mostly been thought to be derived by sprouting from specialized veins. Recently it has been shown that mice deficient for the…”
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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 by 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

“…Prox1 is a transcription factor with two highly conserved domains, a homeobox and a prospero domain. It has been shown that Prox1 knock-out mice die during…”
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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 by 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.

“…Objective The aim of this article is to study secondary cranial signs in fetuses with spina bifida in a precisely defined screening period between 18 + 0 and…”
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Morphological classification of nuchal skin in human fetuses with trisomy 21, 18, and 13 at 12-18 weeks and in a trisomy 16 mouse by von Kaisenberg, C S, Krenn, V, Ludwig, M, Nicolaides, K H, Brand-Saberi, B

“…An increase in the nuchal translucency that can be detected at 10-14 weeks of gestation by ultrasound forms the basis for a screening test for chromosomal…”
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