Results 251 to 260 of about 585,185 (390)

Multiple pregnancy with complete hydatidiform mole and coexisting normal fetus: systematic review and meta‐analysis of clinical outcomes from non‐randomized studies

open access: yesUltrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective Complete hydatidiform mole and coexisting normal fetus (CHMCF) is a rare condition for which there is significant heterogeneity in diagnosis, counseling and management of complications. The objective of this study was to summarize the prevalence of clinical outcomes in reported cases of CHMCF.
N. Salmeri   +8 more
wiley   +1 more source

Correlation Between Serum and Urine β-hCG in Gestational Trophoblastic Neoplasia: A Step Toward Non-Invasive Disease Monitoring. [PDF]

open access: yesInt J Womens Health
Kurniadi A   +6 more
europepmc   +1 more source

A New, Simplified Endoscopic Scoring System for Predicting Clinical Outcome in Gastric Low-Grade Intraepithelial Neoplasia: The “E-Cout System”

open access: green
Nanjun Wang   +10 more
openalex   +1 more source

Diagnostic accuracy of ultrasound models for assessment of ovarian tumors: systematic review and meta‐analysis

open access: yesUltrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective Accurate preoperative classification of ovarian tumors is essential for guiding treatment. There is an increasing body of data evaluating ultrasound‐based models for this purpose in diverse clinical settings. The aim of this systematic review and meta‐analysis was to generate up‐to‐date evidence on the diagnostic accuracy of the most
E. Lems   +7 more
wiley   +1 more source

Table S8 from Exploring the complex relationship between gut microbiota and risk of colorectal neoplasia using bidirectional Mendelian Randomization analysis

open access: gold
Wanxin Li   +19 more
openalex   +1 more source

Diagnosis and medical management of ocular surface squamous neoplasia

open access: yesExpert Review of Ophthalmology, 2017
I. Sayed-Ahmed   +3 more
semanticscholar   +1 more source

Whole‐genome paternal uniparental disomy identified through prenatal single‐nucleotide polymorphism‐based cell‐free DNA screening

open access: yesUltrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective Prenatal single‐nucleotide polymorphism (SNP)‐based cell‐free DNA (cfDNA) screening can identify genome‐wide paternal uniparental disomy (GW‐UPDpat), including cases with complete hydatidiform mole with a coexisting fetus (CHMCF), those with placental mesenchymal dysplasia (PMD) and those with a mosaic/chimeric GW‐UPDpat syndrome ...
P. Benn   +5 more
wiley   +1 more source

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