Y. Oyelese, C. C. Lees, E. Jauniaux
doi : 10.1002/uog.26085
C. Siristatidis, M. Papapanou, V. Karageorgiou, W. P. Martins, I. Bellos, D. M. Teixeira, N. Vlahos
doi : 10.1002/uog.26019
To compare the reported rate of any congenital anomaly and perinatal outcome of pregnancy following blastocyst- vs cleavage-stage embryo transfer using a pairwise meta-analysis and to evaluate the same outcomes following fresh-blastocyst, frozen-blastocyst, fresh-cleavage or frozen-cleavage embryo transfer using a network meta-analysis.
A. Arechvo, A. Wright, A. Syngelaki, P. von Dadelszen, L. A. Magee, R. Akolekar, D. Wright, K. H. Nicolaides
doi : 10.1002/uog.26084
To examine the relationship between the English index of multiple deprivation (IMD) and the incidence of pre-eclampsia (PE), evaluate the distribution of IMD in a cohort of ethnically diverse pregnant women in South East England and assess whether IMD improves the prediction of PE compared with that provided by the ‘history-only’ competing-risks model (based on maternal characteristics and medical history).
J. N. Anderson, R. L. Deter, I. A. Datoc, L. Mack, M. Gandhi, W. Lee, Y. J. Blumenfeld
doi : 10.1002/uog.26102
Previous small studies used individualized growth assessment (IGA) to characterize prenatal growth velocities of singletons and twins. We aimed to compare second-trimester growth velocities of individual anatomical parameters between monochorionic diamniotic (MCDA) twins, dichorionic diamniotic (DCDA) twins and singleton fetuses in a larger study.
C. Vedel, T. D. Hjortshøj, D. S. Jørgensen, A. Tabor, L. Rode, K. Sundberg, C. K. Ekelund, O. B. Petersen
doi : 10.1002/uog.26075
To estimate the prevalence of chromosomal conditions in all fetuses and children with major congenital heart defect (CHD) in Denmark between 2008 and 2018.
T. Miyoshi, Y. Maeno, T. Matsuda, Y. Ito, N. Inamura, K.-S. Kim, I. Shiraishi, K. Kurosaki, T. Ikeda, H. Sago, Collaborators, Japan Fetal Arrhythmia Group
doi : 10.1002/uog.26113
Although many studies have supported the efficacy of transplacental treatment for fetal supraventricular tachyarrhythmia, the long-term neurodevelopmental outcome after antenatal antiarrhythmic treatment is not well understood.
C. Egloff, J. Sibiude, C. Vauloup-Fellous, A. Benachi, E. Bouthry, F. Biquard, A. Hawkins-Villarreal, N. Houhou-Fidouh, L. Mandelbrot, A. J. Vivanti, O. Picone
doi : 10.1002/uog.26039
Congenital cytomegalovirus (CMV) infection is the leading cause of non-genetic hearing and neurological deficits. The aim of our study was to evaluate the efficacy and safety of valacyclovir (VCV) treatment in preventing CMV transmission to the fetus after maternal primary infection.
D. Di Mascio, G. Rizzo, A. Khalil, F. D'Antonio, The ENSO Working Group
doi : 10.1002/uog.26054
To investigate the role of fetal brain magnetic resonance imaging (MRI) in detecting associated anomalies in fetuses with congenital cytomegalovirus (CMV) infection and normal neurosonography.
M. Sanz Cortes, R. Corroenne, B. Johnson, H. Sangi-Haghpeykar, G. Mandy, S. VanLoh, A. Nassr, J. Espinoza, R. Donepudi, A. A. Shamshirsaz, W. E. Whitehead, M. Belfort
doi : 10.1002/uog.26070
To determine if preoperative cervical length in the low–normal range increases the risk of adverse perinatal outcome in patients undergoing fetoscopic spina bifida repair.
L. Joyeux, J. van der Merwe, M. Aertsen, P. A. Patel, A. Khatoun, M. G. M. C. Mori da Cunha, S. De Vleeschauwer, J. Parra, E. Danzer, M. McLaughlin, D. Stoyanov, T. Vercauteren, S. Ourselin, E. Radaelli, P. de Coppi, F. Van Calenbergh, J. Deprest
doi : 10.1002/uog.24907
A contributing factor to unsuccessful prenatal spina bifida aperta (SBA) repair via an open approach may be incomplete neurosurgical repair causing persistent in-utero leakage of cerebrospinal fluid (CSF) and exposure of the fetal spinal cord to amniotic fluid.
A. Dall'Asta, R. Ramirez Zegarra, E. Corno, I. Mappa, J. L. A. Lu, E. Di Pasquo, G. Morganelli, M. Abou-Dakn, C. Germano, R. Attini, B. Masturzo, G. Rizzo, T. Ghi
doi : 10.1002/uog.24981
To evaluate the relationship between the fetal head-circumference-to-maternal-height (HC/MH) ratio measured shortly before delivery and the occurrence of Cesarean section (CS) for labor dystocia.
T. Tellum, B. Bracco, L. V. De Braud, J. Knez, R. Ashton-Barnett, T. Amin, P. Chaggar, D. Jurkovic
doi : 10.1002/uog.26073
To study the reproductive outcomes of women with a unicornuate uterus and compare them to those of women with no congenital uterine anomaly.
E. M. M. Yamaguti, E. T. Sontag dos Reis, W. P. Martins, M. N. Nadai, N. F. Soares, F. da Silva Costa, C. S. Vieira
doi : 10.1002/uog.26023
To describe the feasibility of an ultrasound-guided repositioning technique for partially expelled intrauterine devices (IUDs) without use of sedation.
U. Agarwal, J. Lim, C. Pottinger, E.-K. Suk, R. Chaoui
doi : 10.1002/uog.26062
J. Fourgeaud, B. Regnault, H. Faury, N. Da Rocha, A. Jamet, J. Stirnemann, M. Eloit, P. Perot, M. Leruez-Ville, M. Driessen, Collaborators
doi : 10.1002/uog.26074
C. Keil, I. Bedei, M. Belfort, S. Köhler, M. Sanz Cortes, R. Axt-Fliedner, J. Espinoza
doi : 10.1002/uog.26069
X.-M. Lin, D.-Z. Li
doi : 10.1002/uog.26120
Prenatal genetic testing provides information about the genetic constitution of a fetus, which determines perinatal decision-making and management. Next-generation sequencing has revolutionized the paradigm of clinical genetic testing.
J. Han, D.-Z. Li
doi : 10.1002/uog.26123
Cytomegalovirus (CMV) is the most frequent cause of congenital viral infection, with a prevalence of 0.5–1% among all live births1. Congenital CMV is an important non-hereditary cause of sensorineural hearing loss and neurological deficits.
Y. Matsubara, N. Inamura, N. Takada, T. Fujita
doi : 10.1002/uog.26099
doi : 10.1002/uog.26106
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