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Profil bibliographique

Vivian Kwun Sin Ng

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

5Publications signalées
62Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Maternal and fetal healthcareVenous Thromboembolism Diagnosis and ManagementMuscle Physiology and DisordersMaternal and Perinatal Health InterventionsIon channel regulation and function

Les publications récentes

Accès ouvert 2023 article OpenAlex

Conservative management for placenta accreta spectrum disorders: experience of a regional hospital from 2013 to 2021

Yiu Fai Wong, Tsz Kin Lo, Viola Ying Tze Chan, Vivian Kwun Sin Ng et autres

Introduction: Conservative management by leaving the placenta in situ for placenta accreta spectrum (PAS) disorders can preserve the uterus with reduced surgical complications.This study aims to review the outcomes of planned conservative management for PAS disorders between January 2013 and December 2021. …

cn, hk (code pays fourni par la source)

2 citations Hong Kong Journal of Gynaecology Obstetrics and Midwifery
2022 article OpenAlex

Four cases of cervical varices without placenta praevia: Presentation, diagnosis, managements, and literature review

Chun Kit Wong, Catherine Man Wai Hung, Vivian Kwun Sin Ng, Wai Kuen Yung et autres

Cervical varices are a rare condition characterized by recurrent antepartum hemorrhage and less than 20 cases were reported in the literature. It is usually associated with placenta previa. We herein describe four cases of cervical varices without placenta previa. Meticulous speculum examination, …

cn (code pays fourni par la source)

4 citations Journal of obstetrics and gynaecology research
Accès ouvert 2021 article OpenAlex

A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report

Vivian Kwun Sin Ng, Tze Kin Lau, Anita Sik Yau Kan, Brian Hon‐Yin Chung et autres

Microcephaly and microphthalmia are both rare congenital abnormalities, while concurrently, these two are even rarer. The underlying etiology would be complex interplaying between heterogeneous genetic background and the environmental pathogens, particularly during critical periods of early tissue development. Here, we reported a …

cn, hk (code pays fourni par la source)

2 citations Diagnostics
Accès ouvert 2020 article OpenAlex

The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes

Kit San Yeung, Florrie N. Y. Yu, Cheuk Wing Fung, Sheila Suet-Na Wong et autres

BACKGROUND: Autosomal recessive or compound heterozygous mutations in KLHL40 cause nemaline myopathy 8, which is one of the most severe forms of nemaline myopathy. The KLHL40 c.1516A>C variant has recently been reported as a founder mutation in southern Chinese. METHODS: We report …

hk, gb, cn (code pays fourni par la source)

18 citations Molecular Genetics & Genomic Medicine
2014 article OpenAlex

Relationship between intrapartum transperineal ultrasound measurement of angle of progression and head–perineum distance with correlation to conventional clinical parameters of labor progress and time to delivery

Ying Tze Viola Chan, Vivian Kwun Sin Ng, Wai Kuen Yung, Tsz Kin Lo et autres

OBJECTIVE: To assess whether angle of progression (AOP) and head-perineum distance (HPD) measured by intrapartum transperineal ultrasound (ITU) correlate with clinical fetal head station (station); and whether AOP versus HPD varies during uterine contraction and relaxation. In a subset of primiparous women, …

cn (code pays fourni par la source)

36 citations The Journal of Maternal-Fetal & Neonatal Medicine

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