Results 71 to 80 of about 1,591,948 (303)

Maternal birth experience at operative vaginal birth

open access: yesWomen and Birth
Operative birth is a known risk factor for negative birth experience, yet the modifiable factors that shape these experiences remain underexplored.This study examines factors associated with birth experience following operative second-stage birth, including operative vaginal birth (OVB) or fully dilated caesarean (FDCS).We conducted a prospective mixed-
Sasha M. Skinner   +8 more
openaire   +2 more sources

Estudo comparativo entre histerectomia abdominal e vaginal sem prolapso uterino [PDF]

open access: yes, 2002
Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde. Programa de Pós-Graduação em Ciências Médicas.Objetivo: Comparar a histerectomia abdominal e vaginal sem prolapso ...
Lisboa, Vânio Cardoso
core  

B/ordering and healthcare access for migrants with precarious status: The role of healthcare workers in counteracting restrictive policies

open access: yesAmerican Journal of Community Psychology, EarlyView.
Abstract In Canada, precarious migration is largely invisibilized. Nonetheless, b/ordering greatly affects people's realities by limiting access to social rights. In Quebec, migrants with precarious status (MPS) do not have access to healthcare, although Quebec has a “universal” healthcare coverage.
Émilie Pigeon‐Gagné   +3 more
wiley   +1 more source

Women’s Experiences of Establishing Breastfeeding After Assisted and Unassisted Vaginal Birth

open access: yesProceedings
Vacuum-assisted and forceps-assisted vaginal births are associated with higher rates of formula supplementation and shorter breastfeeding duration compared to unassisted vaginal births; however, the reasons for this are unclear.
Evangeline G. Bevan   +5 more
doaj   +1 more source

Expanded Phenotype Associated With an Intronic PPP1R12A Variant: A Case Report and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal dominant PPP1R12A‐related genitourinary and/or brain malformation syndrome is a recently described multisystem disorder caused by loss‐of‐function variants in the protein phosphatase 1 regulatory subunit 12a (PPP1R12A) gene. To date, 22 affected individuals have been reported with variable brain malformations and genitourinary ...
Emily M. Bland   +4 more
wiley   +1 more source

The interaction between vaginal microbiota, cervical length and vaginal progesterone treatment for preterm birth risk [PDF]

open access: yes, 2016
Background: Preterm birth is the primary cause of infant death worldwide. A short cervix in the second trimester of pregnancy is a risk factor for preterm birth. In specific patient cohorts, vaginal progesterone reduces this risk.
Smith, A   +40 more
core   +1 more source

A Case of Multiple Mitochondrial Dysfunctions Syndrome 1 and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Multiple mitochondrial dysfunctions syndrome 1 (MMDS1, MIM #605711) due to NFU1 gene defects is an ultra‐rare autosomal recessive inborn error of metabolism associated with reduced function of NFU1 iron–sulfur cluster (ISC) scaffold protein.
Charles R. DiFalco   +6 more
wiley   +1 more source

Re-engaging with vaginal breech birth: A philosophical discussion

open access: yes, 2014
The philosophical debate as to whether midwives are equipped to support women requesting vaginal breech birth continues, yet midwives are deemed able to conduct a vaginal breech birth in an ‘emergency’ scenario. The International Breech Birth Conference (
Steele, Dianne, Sanders, Ruth
core   +5 more sources

The ASSIST Study - The BD Odon Device for assisted vaginal birth: a safety and feasibility study

open access: yesTrials, 2019
Background Assisted vaginal birth is a vital health intervention that can result in better outcomes for mothers and their babies when complications arise in the second stage of labour.
Stephen O’Brien   +7 more
doaj   +1 more source

Refining Domain‐Based Prognostication in DNM1 Encephalopathy: A Mild Phenotype Associated With a GTPase Domain Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT DNM1 encephalopathy is a rare autosomal dominant genetic condition characterized by a range of neurological and developmental manifestations. The typical phenotype is severe, including profound intellectual disability, treatment‐resistant epilepsy, ataxia, and structural brain abnormalities. However, milder presentations have increasingly been
Caroline Crain   +6 more
wiley   +1 more source

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