O-8 Investigation of microsatellite instability in human preimplantation embryos von Xanthopoulou, L, Serhal, P, Doshi, A, Delhanty, J.D.A, SenGupta, S

Volltext

Variable aneuploidy mechanisms in embryos from couples with poor reproductive histories undergoing preimplantation genetic screening von Mantzouratou, A., Mania, A., Fragouli, E., Xanthopoulou, L., Tashkandi, S., Fordham, K., Ranieri, D.M., Doshi, A., Nuttall, S., Harper, J.C., Serhal, P., Delhanty, J.D.A.

Volltext

O-078 Mosaic embryos – are they accurately detected by PGT-A? von Popa, T, Whitney, E, Kanani, M, Xanthopoulou, L, Bakosi, E, Davis, C, O'Neill, H, Ottolini, C

Volltext

Chromosome Breakage in Human Preimplantation Embryos from Carriers of Structural Chromosomal Abnormalities in Relation to Fragile Sites, Maternal Age, and Poor Sperm Factors von Xanthopoulou, L., Ghevaria, H., Mantzouratou, A., Serhal, P., Doshi, A., Delhanty, J.D.A.

Volltext

P27 Implementation of array-CGH technology in Preimplantation Genetic Diagnosis for rob(13;14)(q10;q10) Robertsonian translocations von Xanthopoulou, L, Ghevaria, H, Cawood, S, Serhal, P, SenGupta, S.B, Delhanty, J.D.A

Volltext

When is old too old for preimplantation genetic diagnosis for reciprocal translocations? von Xanthopoulou, L., Mantzouratou, A., Mania, A., Ghevaria, H., Ghebo, C., Serhal, P., Delhanty, J. D. A.

Volltext

The nature and origin of binucleate cells in human preimplantation embryos: relevance to placental mesenchymal dysplasia von Xanthopoulou, L, Delhanty, J.D.A, Mania, A, Mamas, T, Serhal, P, SenGupta, S.B, Mantzouratou, A

Volltext

P2 Sex chromosome abnormalities in embryos from women undergoing PGS: Focus on meiotic errors involving the X-chromosome von Ghevaria, H, Mantzouratou, A, Xanthopoulou, L, Serhal, P, Harper, J.C, Delhanty, J.D

Volltext

Session 67: Scientific challenges in early pregnancy achievement von Fouladi-Nashta, A., Marei, W. F., Schust, D., Sugimoto, J., Oda, T., Jinno, Y., Hayashi, Y., Mizutani, E., Kitaori, T., Katano, K., Ozaki, Y., Suzumori, N., Kung, F., Huang, K. H., Hsu, T. Y., Sarasa, J., Enciso, M., Xanthopoulou, L., Bowles, M., Delhanty, J., Wells, D.

Volltext

PGD for an intrachromosomal insertion 7 in a male and a female balanced carrier von Xanthopoulou, L, Mantzouratou, A, Ranieri, DM, Delhanty, J

Volltext

REPRODUCTIVE (EPI) GENETICS von Sertyel, S., Kolankaya, A., Yigit, A., Cengiz, F., Kunacaf, G., Akman, M. A., Gurgan, T., Yu, B., DeCherney, A., Segars, J., Russanova, V., Howard, B., Serafini, P., Kimati, C., Hassun, P., Cuzzi, J., Peres, M., Riboldi, M., Gomes, C., Fettback, P., Alegretti, J., motta, E., Lappa, C., Ottolini, C. S., Summers, M. C., Sage, K., Rogers, S., Griffin, D. K., Handyside, A. H., Thornhill, A. R., Ubaldi, F., Capalbo, A., Wright, G., Elliott, T., Maggiulli, R., Rienzi, L., Nagy, Z. P., Cinar Yapan, C., Beyazyurek, C., Ekmekci, C. G., Altin, G., Yesil, M., Yelke, H., Kahraman, S., Khalil, M., Rittenberg, V., Khalaf, Y., El-toukhy, T., Alvaro Mercadal, B., Imbert, R., Demeestere, I., De Leener, A., Englert, Y., Costagliola, S., Delbaere, A., Zimmermann, B., Ryan, A., Baner, J., Gemelos, G., Dodd, M., Rabinowitz, M., Hill, M., Sandalinas, M., Garcia-Guixe, E., Jimenez-Macedo, A., Gimenez, C., Wemmer, N., Potter, D., Keller, J., Cater, E., Lynch, C., Jenner, L., Berrisford, K., Campbell, A., Keown, N., Rouse, H., Craig, A., Fishel, S., Palomares, A. R., Lendinez Ramirez, A. M., Martinez, F., Ruiz Galdon, M., Reyes Engel, A., Mamas, T., Xanthopoulou, L., Heath, C., Doshi, A., Serhal, P., SenGupta, S. B., Plaza, S., Templin, C., Saguet, F., Claustres, M., Girardet, A., Biricik, A., Colamaria, S., Bono, S., Spizzichino, L., Fiorentino, F., Alegretti, J. R.

Volltext

SELECTED ORAL COMMUNICATION SESSION, SESSION 68: EMBRYOLOGY - THE OOCYTE Wednesday 6 July 2011 14:00 - 15:45 von Vassena, R., Boue, S., Gozalez-Roca, E., Aran, B., Auer, H., Veiga, A., Izpisua Belmonte, J. C., Ermini, B., Stoop, D., Haentjens, P., De Vos, M., Polyzos, N., Verheyen, G., Devroey, P., Montag, M., Ebner, T., Xanthopoulou, L., Mantzouratou, A., Mania, A., Ghevaria, H., Ghebo, C., Serhal, P., Delhanty, J. D. A., Martikainen, H., Niinimaki, M., Suikkari, A. M., Hiraoka, K., Tamaki, T., Matsumura, Y., Kiriake, C., Uto, H., Yoshida, H., Kitamura, S., Monzo, C., Assou, S., Haouzi, D., Bruno, C., Dechaud, H., Hamamah, S.

Volltext

Human susceptibility to aneuploidy and the link to infertility von Mantzouratou, A, Xanthopoulou, L, Mania, A, Tashkandi, S, Harper, JC, Serhal, P, Delhanty, JDA

Volltext

Detection of chromosomal aneuploidy in embryos from PGD cases for monogenic disorders von Mamas, T, Kakourou, G, Dhanjal, S, Cawood, S, Doshi, A, Serhal, P, Xanthopoulou, L, Mantzouratou, A, Delhanty, J, Harper, JC, SenGupta, S

Volltext

Posters Reproductive Genetics (PGD/PGS) von Crippa, A., Magli, M. C., Robles, F., Capoti, A., Ferraretti, A. P., Gianaroli, L., Gallina, A., Bonaparte, E., Moretti, M., Colpi, G. M., Nerva, F., Contalbi, G., Vacalluzzo, L., Tabano, S., Grati, F. R., Gazzano, G., Sirchia, S. M., Simoni, G., Miozzo, M., Handyside, A., Gabriel, A., Thornhill, A. R., Clemente, E., Reitter, C., Affara, N., Griffin, D. K., Macek, M., Feldmar, P., Kluckova, H., Hrehorcak, M., Diblik, J., Paulasova, P., Turnovec, M., Vilimova, S., Fontes, L., Haddad, L., Borges, E., Iaconelli, A., Braga, D. P. A. F., Vianna-Morgante, A. M., Komsky, A., Kasterstein, E., Komarovsky, D., Bern, O., Maslansky, B., Kaplan, T., Raziel, A., Friedler, S., Gidoni, Y., Ben-Ami, I., Ron-El, R., Strassburger, D., Maggiulli, R., Monahan, D., Neri, Q. V., Hu, J. C. Y., Rosenwaks, Z., Palermo, G. D., Beyazyurek, C., Ekmekci, G. C., Tac, H. A., Ajredin, N., Verlinsky, O., Fiorentino, F., Kahraman, S., Camp, M., Hesters, L., Le Lorc'h, M., Frydman, R., Romana, S., Frydman, N., Perez Sanz, J., Matorras, R., Arluzea, J., Romin, Y., Bilbao, J., Gonzalez-Santiago, N., Manova-Todorova, K., Koff, A., Rivera-Pomar, J. M., de la Hoz-Torres, C., Xanthopoulou, L., Ghevaria, H., Mantzouratou, A., Serhal, P., Doshi, A., Delhanty, J. D., Ye, Y., Qian, Y., Jin, F., Munne, S., Gutierrez, C., Wagner, C., Hill, D., Wiemer, K., Fischer, J., Kaplan, B., Danzer, H., Surrey, M., Opsahl, M.

Volltext

Meiotic Behaviour of Chromosomes Involved in Structural Chromosomal Abnormalities Determined by Preimplantation Genetic Diagnosis von Xanthopoulou, L

Volltext

Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy von Enciso, M, Sarasa, J, Xanthopoulou, L, Bristow, S, Bowles, M, Fragouli, E, Delhanty, J, Wells, D

Volltext bestellen

Corneal biomechanics before and after cross-linking in patients with keratoconus von Feld, S, Flockerzi, E, Daas, L, Xanthopoulou, K, Sideroudi, H, Langenbucher, A, Seitz, B

Volltext

Reperfusion therapies and in-hospital outcomes for ST-elevation myocardial infarction in Europe: the ACVC-EAPCI EORP STEMI Registry of the European Society of Cardiology von Zeymer, Uwe, Ludman, Peter, Danchin, Nicolas, Kala, Petr, Laroche, Cécile, Sadeghi, Masoumeh, Caporale, Roberto, Shaheen, Sameh Mohamed, Legutko, Jacek, Iakobsishvili, Zaza, Alhabib, Khalid F, Motovska, Zuzana, Studencan, Martin, Mimoso, Jorge, Becker, David, Alexopoulos, Dimitrios, Kereseselidze, Zviad, Stojkovic, Sinisa, Zelveian, Parounak, Goda, Artan, Mirrakhimov, Erkin, Bajraktari, Gani, Al-Farhan, Hasan, Šerpytis, Pranas, Raungaard, Bent, Marandi, Toomas, Moore, Alice May, Quinn, Martin, Karjalainen, Pasi Paavo, Tatu-Chitolu, Gabriel, Gale, Chris P, Maggioni, Aldo P, Weidinger, Franz

Volltext

Autophagy Blockage Up-Regulates HLA-Class-I Molecule Expression in Lung Cancer and Enhances Anti-PD-L1 Immunotherapy Efficacy von Xanthopoulou, Erasmia, Lamprou, Ioannis, Mitrakas, Achilleas G, Michos, Georgios D, Zois, Christos E, Giatromanolaki, Alexandra, Harris, Adrian L, Koukourakis, Michael I

Volltext