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VERSION:2.0
PRODID:-//Vrije Universiteit Amsterdam//NONSGML v1.0//EN
NAME:PhD defence T.E. König
METHOD:PUBLISH
BEGIN:VEVENT
DTSTART:20260416T134500
DTEND:20260416T151500
DTSTAMP:20260416T134500
UID:2026/phd-defence-t-e-konig@8F96275E-9F55-4B3F-A143-836282E12573
CREATED:20260417T141725
LOCATION:Hoofdgebouw, Aula De Boelelaan 
 1105 1081 HV  Amsterdam
SUMMARY:PhD defence T.E. König
X-ALT-DESC;FMTTYPE=text/html: <html> <body> <p>Ovarian responsiveness 
 to gonadotropins</p> <p>A central theme emerging from this thesis is 
 that ovarian ageing and ovarian responsiveness are the result of a co
 mplex interplay between follicle quantity, oocyte quality, endocrine 
 regulation, and genetic variation. While ovarian reserve tests inform
  expectations regarding stimulation outcomes, they do not solely dete
 rmine reproductive potential. Similarly, although genetic variants in
  FSHR modulate ovarian sensitivity, they do not significantly influen
 ce live birth outcomes nor justify routine dose escalation. The studi
 es presented in this thesis further demonstrate that diminished ovari
 an reserve does not equate to a lack of functional ovarian responsive
 ness. Overall, the findings support a cautious, individualized, and e
 vidence-based approach to ovarian stimulation, in which age, ovarian 
 reserve, and biological variability are jointly considered, rather th
 an relying on single biomarkers or empiric dose escalation.</p><p>Mor
 e information on the <a href="https://hdl.handle.net/1871.1/45d37537-
 db7c-4a91-89e3-cf58e248870b" data-new-window="true" target="_blank" r
 el="noopener noreferrer">thesis</a></p> </body> </html>
DESCRIPTION: A central theme emerging from this thesis is that ovarian
  ageing and ovarian responsiveness are the result of a complex interp
 lay between follicle quantity, oocyte quality, endocrine regulation, 
 and genetic variation. While ovarian reserve tests inform expectation
 s regarding stimulation outcomes, they do not solely determine reprod
 uctive potential. Similarly, although genetic variants in FSHR modula
 te ovarian sensitivity, they do not significantly influence live birt
 h outcomes nor justify routine dose escalation. The studies presented
  in this thesis further demonstrate that diminished ovarian reserve d
 oes not equate to a lack of functional ovarian responsiveness. Overal
 l, the findings support a cautious, individualized, and evidence-base
 d approach to ovarian stimulation, in which age, ovarian reserve, and
  biological variability are jointly considered, rather than relying o
 n single biomarkers or empiric dose escalation. More information on t
 he <a href="https://hdl.handle.net/1871.1/45d37537-db7c-4a91-89e3-cf5
 8e248870b" data-new-window="true" target="_blank" rel="noopener noref
 errer">thesis</a> Ovarian responsiveness to gonadotropins
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