Results 41 to 50 of about 57,391 (186)
Congenital imperforate hymen with hydrocolpos and hydronephrosis associated with severe hydramnios and increase of maternal ovarian steroidogenic enzymes [PDF]
This is a clinical research paperStudy Objective: To study clinical features of patient presented with severe hydramnios, associated with hydronephrosis, that was antenatally diagnosed and has been successfully treated immediately after birth.
Foster, H +3 more
core +1 more source
Ovarioleukodystrophy due to EIF2B5 mutations [PDF]
Ovarioleukodystrophy – the co-occurrence of leukodystrophy and premature ovarian failure – is a rare presentation which is now recognised to be part of the clinical spectrum of vanishing white matter disease.
Faulkner, Howard +4 more
core +2 more sources
Background Ovarian antibodies as detected by indirect immunofluorescence have been used to detect ovarian autoimmunity, but to our knowledge the rate of false positive findings using this method has never been reported.
Nelson Lawrence M +3 more
doaj +1 more source
The effects of uterine artery embolisation and surgical treatment on ovarian function in women with uterine fibroids [PDF]
Objective The aim of this study was to evaluate and compare both ovarian function and menstrual characteristics following uterine artery embolisation (UAE) and surgery. Design Subgroup of women from a randomised controlled trial.
Beavis +23 more
core +1 more source
Traditional Chinese Medicine and Its Role in Women’s Health [PDF]
This paper is a literature review of traditional Chinese medicine and its role in women’s health. A search was performed and a group of 208 articles were initially found using the Liberty Summons search engine.
Smith, Ezekiel
core +1 more source
A hidden cause of infertility in hypothyroid patients [PDF]
Methylene tetrahydrofolate reductase (MTHFR) gene mutations could be the cause of infertility in hypothyroid patients. Hence, it is worthy to screen for MTHFR gene mutations in infertile hypothyroid females and their partners if infertility persists ...
Ahmed, Soha Magdy +4 more
core +1 more source
Objective: To investigate markers of premature menopause (
Elinor Chelsom Vogt +23 more
doaj +1 more source
CSB-PGBD3 Mutations Cause Premature Ovarian Failure. [PDF]
Premature ovarian failure (POF) is a rare, heterogeneous disorder characterized by cessation of menstruation occurring before the age of 40 years. Genetic etiology is responsible for perhaps 25% of cases, but most cases are sporadic and unexplained.
Yingying Qin +10 more
doaj +1 more source
Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis [PDF]
Meiosis is unique to germ cells and essential for reproduction. During the first meiotic division, homologous chromosomes pair, recombine, and form chiasmata.
Choi, Y +8 more
core +5 more sources
Premature ovarian failure: problems and prospects (literature review)
Relevance. Premature ovarian failure is a condition characterized by loss of ovarian function in women under 40 years of age, occurring against the background of dysfunction or depletion of ovarian follicles, which leads to oligo/amenorrhea ...
Tatyana Yu. Pestrikova +1 more
doaj +1 more source

