Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Hayri Ermiş"'
Autor:
Alkan Yildirim, Atıl Yüksel, Cenk Yasa, Lemi Ibrahimoglu, Hayri Ermiş, Ibrahim Kalelioglu, Ozlem Dural, Esra Gilbaz Akel, Recep Has, Aytul Corbacioglu Esmer
Publikováno v:
Journal of Clinical Ultrasound. 44:106-112
Purpose The aim of this prospective observational study was to identify the best method for use in diagnosing fetal nasal bone (NB) hypoplasia in the second trimester as a means of predicting trisomy 21 (Down syndrome). Methods The NB length (NBL), N
Autor:
Ismail Dolekcap, Kılıç Aydınlı, Mohammad Kazem Hosseini, Ali Benian, Ibrahim Kalelioglu, Görkem Zeybek, Ece Gumusoglu, Hayri Ermiş, Tuba Gunel
Publikováno v:
Turkish Journal of Obstetrics and Gynecology
Turkish Journal of Obstetrics and Gynecology, Vol 11, Iss 4, Pp 233-241 (2014)
Turkish Journal of Obstetrics and Gynecology, Vol 11, Iss 4, Pp 233-241 (2014)
Recent developments in molecular genetics improved our knowledge on fetal genome and physiology. Novel scientific innovations in prenatal diagnosis have accelerated in the last decade changing our vision immensely. Data obtained from fetal genomic st
Autor:
Alkan Yildirim, Harika Yumru, Lemi Ibrahimoglu, Hayri Ermiş, Ozlem Dural, Ibrahim Kalelioglu, Ömer Faruk Demir, Y. Dogan, Cenk Yasa, Recep Has, Atιl Yuksel, Aytul Corbacioglu Esmer
Publikováno v:
Fetal Diagnosis and Therapy. 36:190-195
Aim: To report our experience in selective termination of monochorionic twin pregnancies with bipolar cord coagulation and to analyze the pregnancy outcomes and complications based on the indication of the procedure. Methods: This is a retrospective
Autor:
Ömer Faruk Demir, Cenk Yasa, Y. Dogan, Alkan Yildirim, Hayri Ermiş, Atıl Yüksel, Ozlem Dural, Lemi Ibrahimoglu, Ibrahim Kalelioglu, Recep Has, Harika Yumru, Aytul Corbacioglu Esmer
Publikováno v:
Fetal Diagnosis and Therapy. 36:287-292
Aim: To review the perinatal outcome of twin-to-twin transfusion syndrome (TTTS) treated with fetoscopic laser coagulation in a developing country with detailed analysis according to the stage of the syndrome. Methods: This was a retrospective study
Autor:
Linda Wu, Andrew McLennan, Jennifer Sanderson, Ahm Kim, Faisal Qureshi, Irene T.M. Lindenburg, Aditi Majajan, Alkan Yildirim, Amanda Henry, Kara Juneau, Linus Bjäreborn, Suzanne M. Jacques, Magnus Nordenskjöld, Alma Aurioles-Garibay, Atıl Yüksel, Inge L. van Kamp, Satz Mengensatzproduktion, Ömer Faruk Demir, N. Scott Adzick, Roberto Romero, Patrick E. Bogard, Karin Pettersson, Mi-Young Lee, Mark P. Johnson, William H. Peranteau, Eric T. Wang, Druckerei Stückle, Gus Ridding, Sonia S. Hassan, Lemi Ibrahimoglu, Ibrahim Kalelioglu, John M.G. van Vugt, Kyu-Sang Kyeong, Harika Yumru, Nahla Khalek, Christopher Kingsley, Craig A. Struble, Annegret Geipel, Jae-Yoon Shim, Christoph Berg, Heiko Reutter, Maynor Garcia, Morassa Mohseni, Aytul Corbacioglu Esmer, Marinus A. Blankenstein, Hayri Ermiş, Tinnakorn Chaiworapongsa, Beverly G. Coleman, Jos W. R. Twisk, Paul Ryvkin, Peter Gustavsson, Lami Yeo, Alan W. Flake, Nikos Papadogiannakis, Cenk Yasa, Neama Meriki, Y. Dogan, Pil Ryang Lee, Recep Has, Ulrich Gembruch, Michael R. Mallmann, Lori J. Howell, Teresa Victoria, Hye-Sung Won, Andreas Müller, Ozlem Dural, Edgar Hernandez-Andrade, Holly L. Hedrick, Jacob Zahn, Jesse D. Vrecenak, Erik Iwarsson, Philip J. Schluter, Jon Hyett, Melanie A. J. Engels, Dick Oepkes, Hyunyoung Ahn, Stephanie Huang, Ellika Sahlin, Arnold Oliphant, Julie S. Moldenhauer, Agne Liedén, Alec W. Welsh, Thomas M. Boemers
Publikováno v:
Fetal Diagnosis and Therapy. 36:I-IV
Publikováno v:
Genetics and Molecular Research. 10:2653-2657
Hemolytic disease of the newborn is a clinical condition in which maternal and paternal Rh blood group antigens are incompatible and the mother is negative for the antigen whereas the father is positive. Analysis of fetal cells recovered from materna
Publikováno v:
Journal of the Turkish-German Gynecological Association, Vol 11, Iss 02, Pp 82-85 (2010)
Hemolytic disease of the newborn (HDN) is a clinic phenomenon which occurs during pregnancy due to the Rhesus (Rh) D alloimmunization between a Rh (-) pregnant woman, who has become sensitive to RhD antigens, and her Rh (+) fetus. As a result of the
Publikováno v:
Prenatal Diagnosis. 23:336-339
The short-stature homeobox-containing gene (SHOX) on chromosome Xp22.3 was recently identified as an important determinant of the stature phenotype. Deletions of the SHOX gene, some of them due to structural chromosome abnormalities, have been descri
Publikováno v:
Biotechnology & Biotechnological Equipment. 26:2913-2915
The antepartum and peripartum maternal infections cause great problems complicating pregnancy. The early diagnosis of the maternal infections causing different pathologies in the newborns is of gre...
Autor:
Recep Has, Alkan Yildirim, T. Sarac Sivrikoz, Atıl Yüksel, Halime Çali, Hayri Ermiş, Lemi Ibrahimoglu, Z. Sahinoglu, Ibrahim Kalelioglu
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 46:220-221