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P Devroey

Showing results (391-400 of 406) with videos related to

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Contributions to Gynecology and Obstetrics|January 1, 1987
Gamete intra-fallopian transfer versus in vitro fertilization and embryo transfer in endometriosisP Devroey, P Braeckmans, M Camus, et al.
Human Reproduction Update|September 8, 2011
Contemporary genetic technologies and female reproduction, B C J M Fauser, K Diedrich, et al.
Human Reproduction (Oxford, England)|October 1, 1988
Hyperstimulation: the need for cryopreservation of embryosE Van den Abbeel, J Van der Elst, L Van Waesberghe, et al.
Archives of Gynecology and Obstetrics|May 10, 2002
Plasma and follicular fluid concentrations of LHRH antagonist cetrorelix (Cetrotide) in controlled ovarian stimulation for IVFM Ludwig, C Albano, F Olivennes, et al.
Molecular Human Reproduction|June 13, 2003
Preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1AA De Vos, K Sermon, M De Rijcke, et al.
Human Reproduction (Oxford, England)|October 26, 2011
The reliability of the histological diagnosis of endometritis in asymptomatic IVF cases: a multicenter observer studyJ C Kasius, F J M Broekmans, D M D S Sie-Go, et al.
Human Reproduction (Oxford, England)|November 15, 2005
Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disordersI Mateizel, N De Temmerman, U Ullmann, et al.
Human Reproduction (Oxford, England)|February 12, 2011
Observer agreement in the evaluation of the uterine cavity by hysteroscopy prior to in vitro fertilizationJ C Kasius, F J M Broekmans, S Veersema, et al.
Human Reproduction (Oxford, England)|June 26, 2016
Ovarian hyperstimulation syndrome: review and new classification criteria for reporting in clinical trialsP Humaidan, S M Nelson, P Devroey, et al.
Molecular Human Reproduction|August 6, 2003
Improving clinical preimplantation genetic diagnosis for cystic fibrosis by duplex PCR using two polymorphic markers or one polymorphic marker in combination with the detection of the DeltaF508 mutationV Goossens, K Sermon, W Lissens, et al.
Pageof 41

Showing results (391-400 of 406) with videos related to

Sort By:
Pageof 41
Contributions to Gynecology and Obstetrics|January 1, 1987
Gamete intra-fallopian transfer versus in vitro fertilization and embryo transfer in endometriosisP Devroey, P Braeckmans, M Camus, et al.
Human Reproduction Update|September 8, 2011
Contemporary genetic technologies and female reproduction, B C J M Fauser, K Diedrich, et al.
Human Reproduction (Oxford, England)|October 1, 1988
Hyperstimulation: the need for cryopreservation of embryosE Van den Abbeel, J Van der Elst, L Van Waesberghe, et al.
Archives of Gynecology and Obstetrics|May 10, 2002
Plasma and follicular fluid concentrations of LHRH antagonist cetrorelix (Cetrotide) in controlled ovarian stimulation for IVFM Ludwig, C Albano, F Olivennes, et al.
Molecular Human Reproduction|June 13, 2003
Preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1AA De Vos, K Sermon, M De Rijcke, et al.
Human Reproduction (Oxford, England)|October 26, 2011
The reliability of the histological diagnosis of endometritis in asymptomatic IVF cases: a multicenter observer studyJ C Kasius, F J M Broekmans, D M D S Sie-Go, et al.
Human Reproduction (Oxford, England)|November 15, 2005
Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disordersI Mateizel, N De Temmerman, U Ullmann, et al.
Human Reproduction (Oxford, England)|February 12, 2011
Observer agreement in the evaluation of the uterine cavity by hysteroscopy prior to in vitro fertilizationJ C Kasius, F J M Broekmans, S Veersema, et al.
Human Reproduction (Oxford, England)|June 26, 2016
Ovarian hyperstimulation syndrome: review and new classification criteria for reporting in clinical trialsP Humaidan, S M Nelson, P Devroey, et al.
Molecular Human Reproduction|August 6, 2003
Improving clinical preimplantation genetic diagnosis for cystic fibrosis by duplex PCR using two polymorphic markers or one polymorphic marker in combination with the detection of the DeltaF508 mutationV Goossens, K Sermon, W Lissens, et al.
Pageof 41