Zobrazeno 1 - 10
of 141
pro vyhledávání: '"I. Tekesin"'
Autor:
I. Tekesin, Oliver Graupner
Publikováno v:
Journal of clinical ultrasound : JCUREFERENCES. 49(2)
PURPOSE This retrospective study aims to determine whether the maxilla-mandible-nasion (MMN) angle can be reliably measured in the first trimester, to describe normal ranges, and to determine if significant changes occur in foetuses with aneuploidies
Autor:
O Graunpner, I Tekesin
Publikováno v:
Ultraschall in der Medizin - European Journal of Ultrasound.
Autor:
I. Tekesin, Oliver Graupner
Publikováno v:
Journal of perinatal medicine. 47(9)
ObjectiveTo determine whether the measurement of inferior facial angle (IFA) and prefrontal space ratio (PFSR) in two-dimensional (2D) ultrasound images in the first trimester of pregnancy is reliable and to describe these markers in normal and aneup
Autor:
O Graupner, I Tekesin
Publikováno v:
Interdisziplinärer Kongress | Ultraschall 2018 – 42. Dreiländertreffen SGUM | DEGUM | ÖGUM.
Autor:
I Tekesin
Publikováno v:
Interdisziplinärer Kongress | Ultraschall 2018 – 42. Dreiländertreffen SGUM | DEGUM | ÖGUM.
Autor:
I. Tekesin
Publikováno v:
Journal of perinatal medicineReferences. 47(2)
Objectives To assess the diagnostic value of an early anomaly scan in fetuses with increased nuchal translucency (NT) in the prediction of aneuploidy. Methods In this study we analyzed the data of pregnant women obtained at their first trimester scre
Autor:
I. Tekesin, F. Uhlemann
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 51:274-275
Autor:
V. Pietzsch, B. Benoit, Rabih Chaoui, A. Sarut Lopez, Karl O. Kagan, Kai-Sven Heling, I. Tekesin, K. Karl
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 38:722-726
We describe a case series of six fetuses with open spina bifida (OSB) from four different prenatal units, where the anomaly was detected at the routine 11-13-week ultrasound examination. Crown-rump length ranged from 49 to 78 mm. All cases were first
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Autor:
M. Duchoslav, M. Guillaud-Bataille, R. Weikard, A.M. Dutrillaux, R.M. Brunner, P. Parma, B. Dutrillaux, S. Brüderlein, J. Dolezel, S. Ganapathiraju, C. Denis, L.-J. Hsieh, H. Xie, E. Hřibová, T.F. Barth, D.L. Adelson, L. De Lorenzi, C. Richon, Ö. Altug-Teber, S. Toujani, A.A. Schäffer, M.J. Puertas, T.L. Lear, J.E. Womack, M. Cuacos, M. Walter, G.P. Di Meo, S.-L. Shi, T. Goldammer, K.G. Heller, M.D. Mudry, L. Iannuzzi, S.A. Brooks, P. Möller, A. Viardot, E. Bailey, J. Macas, I. Tekesin, S. Wegener, M.N. Miziara, A.C. Brasileiro-Vidal, L. Molteni, D. Incarnato, R.-H. Teng, M.E.J. Amaral, H. Mozdarani, Y.-C. Li, R. Berger, J. Doležel, A. Eggen, A. Bernheim, H. Waxin, M. Bonin, A.J. Lukaszewski, F.-J. Tsai, L.J. Campbell, D.S. Perez, P. Vosough, D.I. Smith, Y.-M. Cheng, A.D. Bolzán, D. Kopecky, P.-P. Liu, C.C. Lin, I. Melzner, D.C. Allen, O. Riess, R. Brunner, R. Agarwala, C.D. James, H.K. Müller-Hermelink, M. González-García, R.R. Lemos, J.M. Vega, S. McAvoy, K. Nieselt, A. Perucatti, S. Debarshi, H. Heilbronner, W. dos S. Soares Filho, S. Popov, M. Volleth, M. Doleželová, A. De Giovanni, M. González-Sánchez, U.A. Mau-Holzmann, C.D. Town, M. Nieves, A. Mohseni-Meybodi, R.N. MacKinnon, M. Guerra, K.N. Mohan, B.S. Rani, M. Rosato, S. Selvam, A. Mader, P. Dessen, J.S. Kadandale, A.P. Moraes, A. Dufke, H. Stappert
Publikováno v:
Cytogenetic and Genome Research. 119:I-IV