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10.1007/s10815-013-0164-1 http://scihub22266oqcxt.onion/10.1007/s10815-013-0164-1 C3969462!3969462!24390627     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Assist+Reprod+Genet 2014 ; 31 (4): 447-51 Nephropedia Template TP {{tp|p=24390627|t=2014. Vitrification of human blastocysts previously cryopreserved by slow controlled-rate freezing at the cleavage stage |pdf=|usr=}}{{24390627}} gab.com Text Vitrification of human blastocysts previously cryopreserved by slow controlled-rate freezing at the cleavage stage JO: J Assist Reprod Genet http://www.kidney.de/pget.php?&tw=1&pmid=24390627 #FOAvip Purpose: The objective of this study was to evaluate the efficiency of vitrified blastocysts derived from frozen-thawed cleavage stage embryos in terms of morphological survival and re-expansion status of the blastocoelic cavity. Results: After warming 162 blastocysts derived from fresh embryos (= control group) and 90 blastocysts from frozen-thawed cleavage stage embryos (= study group) and after 2?3 h of in vitro culture the percentage of blastocysts with morphological survival was not different between the two groups. After 24 h of in vitro culture, the percentage of fully expanded, hatching or hatched blastocysts was not different between both groups. Conclusion(s): The results show that blastocysts derived from frozen-thawed cleavage stage embryos can be cryopreserved successfully a second time by vitrification method. Re-cryopreservation by vitrification still needs to be approached with some caution because little data on long term safety of multiple freezing is available. Twit Text FOAVip Vitrification of human blastocysts previously cryopreserved by slow controlled-rate freezing at the cleavage stage ????J Assist Reprod Genet http://www.kidney.de/pget.php?&tw=1&pmid=24390627 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24390627 #FOAvip English Wikipedia <ref>{{Cite pmid|24390627}}</ref> Vitrification of human blastocysts previously cryopreserved by slow controlled-rate freezing at the cleavage stage #MMPMID24390627 Lierman S; Van den Abbeel E; De Sutter P J Assist Reprod Genet 2014[Apr]; 31 (4): 447-51 PMID24390627show ga Purpose: The objective of this study was to evaluate the efficiency of vitrified blastocysts derived from frozen-thawed cleavage stage embryos in terms of morphological survival and re-expansion status of the blastocoelic cavity. Results: After warming 162 blastocysts derived from fresh embryos (= control group) and 90 blastocysts from frozen-thawed cleavage stage embryos (= study group) and after 2?3 h of in vitro culture the percentage of blastocysts with morphological survival was not different between the two groups. After 24 h of in vitro culture, the percentage of fully expanded, hatching or hatched blastocysts was not different between both groups. Conclusion(s): The results show that blastocysts derived from frozen-thawed cleavage stage embryos can be cryopreserved successfully a second time by vitrification method. Re-cryopreservation by vitrification still needs to be approached with some caution because little data on long term safety of multiple freezing is available. äVitrification of human blastocysts previously cryopreserved by slow co(epmc).pdf DeepDyve Pubget Overpricing