Results 181 to 190 of about 533,253 (303)
ABSTRACT Background Homecare aides (HCAs) are professional non‐family caregivers, who support dependent individuals to live at home with dignity; yet in Spain they remain understudied and vulnerable, often facing precarious working conditions. We aimed to characterize HCAs’ employment, living conditions, health, and exposure to workplace violence and ...
Albert Navarro‐Giné +6 more
wiley +1 more source
Beyond choice: social realities shaping pregnancy decisions and family planning agency among Black women in the south. [PDF]
Thompson TA +4 more
europepmc +1 more source
ABSTRACT Objective Construction workers face elevated risks of alcohol misuse—especially binge drinking—due to physically demanding labor, long hours, and limited paid vacation. At the same time, emerging evidence suggests that a larger local construction sector may have protective community‐level effects on alcohol and other drug outcomes.
Sehun Oh +2 more
wiley +1 more source
Listening to Unheard Voices: Addressing Systemic Racism to Improve Maternity Care for Black Women After Perinatal Loss. [PDF]
Antilla JM +4 more
europepmc +1 more source
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli +11 more
wiley +1 more source
Breast Cancer Characteristics and Outcomes in Canadian Black Women by Ancestry. [PDF]
Wilkinson AN +4 more
europepmc +1 more source
Unraveling a Diagnostic Enigma: A TECPR2 Case Solved Through Multi‐Omic Genomics
ABSTRACT TECPR2 is a key regulator of autophagy, encoded by the TECPR2 gene. Pathogenic variants in this gene have been linked to a rare hereditary sensory and autonomic neuropathy with intellectual disability (HSAN9). We report a teenage female with a syndromic intellectual disability disorder associated with neuromuscular abnormalities.
Teresa Zhao +122 more
wiley +1 more source
The paradox of action: Trajectories in distress, meaning, and gene regulation following self-directed activist engagement among Black women. [PDF]
Geyton TA, Cole SW.
europepmc +1 more source
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu +23 more
wiley +1 more source

