Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Sanyukta Runkel"'
Publikováno v:
Clinical Genetics. 52:96-99
We report here a case of partial trisomy of the short arm of chromosome 3 combined with partial monosomy 5p due to malsegregation of a balanced maternal translocation t(3;5). The newborn demonstrated esophageal atresia and complex cerebral malformati
Autor:
Sanyukta Runkel, Gilbert Schönfelder, Achim Schneider, Jörn Rentzsch, Christiane Richter-Ehrenstein
Publikováno v:
Breast Cancer Research and Treatment. 106:343-349
Development of new capillary blood vessels is essential for the growth of cancer. Two distinct processes, vasculogenesis and angiogenesis implement the formation of the new vascular network. Recently, it was demonstrated that vasculogenesis creates t
Publikováno v:
Fetal Diagnosis and Therapy. 13:35-38
Advances in ultrasound technology and sonographer’s experience lead to the description of many rare syndromes and malformations through prenatal diagnosis. Diaphragmatic hernia is a rather common malformation but can be an indicator of different sy
Autor:
M.F. Press, T. Cunze, H.J. Schröder, W. Lichtenegger, E. Halberstadt, T. Schill, Nadia Harbeck, A. Huber, A. Fischer, A. von Daimling, T. Strohmeyer, Ch. Thomssen, C. Zoll, C. Marth, R. Lissner, P.G. Knapstein, D. Macchiella, G. Daxenbichler, T. Beck, B. Wartusch, H. Günes, B. Föst, R. Conradi, F. Kainer, O. Dapunt, E. Petru, W. Friedmann, C. Villena-Heinsen, U. Schwuléra, G. Büge, G.B. Lipford, A. Lopens, T. Nebe, G. Huber, G. Weber, R. Höpfl, S. Anthuber, S. Al-Hasani, Klara Fizi, L. Pache, S. Wilhelm, W.G. Rossmanith, A. Schiller, B. Gerber, U. Ulrich, O. Wilhelm, P. Berger, B. Lechner, E. Kaiserling, W. Schmidt, W. Küpker, J.W. Kreider, M. Frank, A. Luttkus, Sanyukta Runkel, B. Djuricic, P. Dettmar, W. Kuhn, W. Nathrath, M. Neises, H. Schaider, H.G. Bender, W. Kühnel, H. Graeff, S. Ditz, E. Bierhoff, P. Mallmann, J. Bläser, R. Felberbaum, C. Rybakowski, A. Jensen, A. Bergant, K. Marzusch, J.W. Dudenhausen, W. Weikel, G. Fleckenstein, S. Herzog, B.U. Sevin, K. Heim, H.-P. Horny, S. Rimbach, N. Ruth, N.D. Christensen, K. Ulm, E. Merz, Veronika Schlamp, H. Meden, J. Keckstein, R. Kimmig, J. Haas, W. Bunk, D. Wallwiener, E. Çetin, K. Diedrich, M.P. Dierich, Annette Krause, G.E. Morfill, F. Melchert, W. Rath, R. Moll, H. Tschesche, Andrea Steinbron, A. Wischnik, R. Berger, W. Wuttke, W. Schröder, M. Cervar, Ch. Sohn, S. Mielke, U. Janssen, P. Ruck, Cosima Brucker, K. Maag, O.D. Wiestler, M. Kolben, G. Bastert, H. Zwierzina, C. Brumm, E. Melchert, C. Anthuber, K. Wayss, M. Schmitt, B. Hüneke, Antje Keberle, Rita K. Schmutzler, D. Krebs, T. Reissmann, B. Aydeniz, G.v. Herder, W. Schulze, G. Kuhn, W. Paschen, J. Gnirs, G. Desoye, I. Tossounidis, F. Bahlmann, C. Larcher, Petra Ziffer, K.T.M. Schneider, J. Dietl, S. Meyer, F. Jänicke, R. Osmers, G. Pirschner, U. Bartels, C. Diedrich, Angela Reles, A. Zeimet, A. Homann, R. Handgretinger, Ines Schönborn, K. Friese, I. Pündmann, D. Labeit, D. Mink
Publikováno v:
Gynäkologisch-geburtshilfliche Rundschau. 35:I-IV
Publikováno v:
Gynäkologisch-geburtshilfliche Rundschau. 35:68-72
Fragestellung: Die Vaskularisation bei Mammakarzinomen hat sich als ein unabhangiger Prognoseparameter erwiesen. Diese Arbeit untersucht am menschlichen Mammakarzinom die Neo-Vaskularisation und das Tumorwachstum im Xenotransplantat und die Gewebsoxy
Publikováno v:
Clinical Genetics. 57:148-150
Larsen syndrome shows a broad spectrum of clinical manifestation ranging from a lethal form of the disorder to a mild clinical expression with absence of major diagnostic features. Here we show that even intrafamilial manifestation may vary extremely
Publikováno v:
Fetal Diagnosis and Therapy. 15:301-303
We report on a case of embryonic anomaly detected at 9 + 5 gestational weeks. The lower part of the embryo was located in the coelomic cavity. Lower extremities could not be depicted. The abdominal wall showed the appearance of omphalocoele. After te
Publikováno v:
International Journal of Radiation Biology. 60:65-70
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 84:111-113
The coincidence of HELLP syndrome and cortical blindness is an uncommon but very dramatic event, for the patient as well as the obstetrician. This report describes the first case of HELLP-syndrome-associated cortical blindness occuring suddenly in th
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 79:99-101
We present a case of congenital cystic adenomatoid malformation of the lung (CCAM) diagnosed at 23 weeks of gestation with concomitant fetal hydrops. The sonographical picture of CCAM disappeared in the third trimester of pregnancy and fetal hydrops