Ovarian insufficiency
Genetics pathogenesis in the ovarian insufficiency
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A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing
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The significance of FMR1 CGG repeats in Chinese women with premature ovarian insufficiency and diminished ovarian reserve
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Original Article Correlation of serum vitamin D levels with ovarian reserve markers in patients with primary ovarian insufficiency
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Primary ovarian insufficiency in a xeroderma pigmentosum patient with consanguineous parents
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Successful pregnancy with donor eggs in-vitro fertilization after premature ovarian insufficiency in a tertiary hospital in a low-income setting: a case report
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THE ROLE OF GENE THERAPY IN PREMATURE OVARIAN INSUFFICIENCY MANAGEMENT
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ABSTRACT: Ovarian hypofunction or primary ovarian insufficiency (POI) is a common
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Blepharophimosis ptosis epicanthus inversus syndrome (BPES): A rare cause of primary ovarian insufficiency
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Primary ovarian insufficiency: different approaches in three cases and a review of literature
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Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation
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Occult Form of Premature Ovarian Insufficiency in Women with Infertility and Oligomenorrhea as Assessed by Poor Ovarian Response Criteria
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Effects of FSHR polymorphisms on premature ovarian insufficiency in human beings: a meta-analysis
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Original Article Ovarian IL-1α and IL-1β levels are associated with primary ovarian insufficiency
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Role of microRNAs in premature ovarian insufficiency
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Human amnion-derived mesenchymal stem cell (hAD-MSC) transplantation improves ovarian function in rats with premature ovarian insufficiency (POI) at least partly through a paracrine mechanism
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Primary ovarian insufficiency: an update
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No association between polymorphisms in PTEN and primary ovarian insufficiency in a Han Chinese population
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Primary Ovarian Insufficiency and Adolescent Vaccination
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Fertility Preservation in Premature Ovarian Insufficiency (POI) Secondary to FSH Receptor Gene (FSHR) Mutation: Is There a New Hope?
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