Results 111 to 120 of about 3,699 (217)
Uterus transplantation: an experimental study in the rat model [PDF]
One of the last frontiers to conquer in infertility research is to find a treatment for uterine factor infertility, which affects around 2500 Swedish women. These women cannot become pregnant or carry a pregnancy due to absence of uterus or presence of
Akhi, Musammad Shamima Nazmin
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Development of the human prepuce and its innervation. [PDF]
Development of the human prepuce was studied over the course of 9-17 weeks of gestation in 30 specimens. Scanning electron microscopy revealed subtle surface features that were associated with preputial development, namely the appearance of epidermal ...
Baskin, Laurence S +3 more
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A Case of Late-Diagnosed Ovotesticular Disorder of Sex Development [PDF]
We report acase of!ovotesticular disorder of sex development!(DSD) with ambiguous genitalia, 46XX presenting the clinical, laboratory, imaging and operative findings and highlighting the pertinent features of this case.
Alves, F +7 more
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A case of septate uterus with double cervix and longitudinal septum of vagina [PDF]
The incidence of Mullerian duct anomalies is around 3% in patients with infertility or poor reproductive outcomes. Most Mullerian duct anomalies are associated with a single cervix.
Držislav Kalafatić +2 more
core +1 more source
Морфогенез маткових труб у перинатальному періоді онтогенезу людини [PDF]
Антенатальна діагностика, хірургічна корекція i профілактика патології плода – найсуттєвіший компонент репродуктивної стратегії та перинатології [1, 2].
Ахтемійчук, Юрій Танасович +2 more
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RARE MULLERIAN DUCT ANOMALY: ASYMMETRIC SEPTATE UTERUS
Robert's uterus (asymmetric septate uterus) is a rare and unique Mullerian duct anomaly, first reported by Robert H. in 1970. This malformation shows two uterine hemicavities, one being blind, causing hematometra, and the other cavity is communicating to a single cervix.
openaire +1 more source
Meckel-Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe [PDF]
Meckel-Gruber Syndrome is a rare autosomal recessive lethal ciliopathy characterized by the triad of cystic renal dysplasia, occipital encephalocele and postaxial polydactyly.
Addor, Marie-Claude +18 more
core +1 more source
A rare case of OHVIRA (obstructed hemivagina and ipsilateral renal anomaly) syndrome: Case report
Obstructed hemivagina and ipsilateral renal anomaly syndrome (OHVIRA) also known as Herlyn-Werner-Wunderlich syndrome is a rare type of Müllerian duct anomaly with concomitant mesonephric duct anomalies.
Natnael Alemu Bezabih +3 more
doaj +1 more source
Ovarian malignancy in a patient with Herlyn–Werner–Wunderlich syndrome: A rare clinical presentation
Herlyn–Werner–Wunderlich Syndrome (HWWS) is a rare congenital Mullerian duct anomaly, characterized by the presence of an obstructed hemivagina with uterus didelphys and an ipsilateral renal anomaly (OHVIRA).
Gilana Abinales Gonzales +1 more
doaj +1 more source
Progression of the field depends on convergence of information technology, operational technology and protocol-agnostic telecommunications. Making sense of the data, ability to curate data and perform data analytics at the edge (or mist rather than in ...
Datta, Shoumen
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