Results 41 to 50 of about 1,755,813 (344)

"Mothers as Candy Wrappers": Critical Infrastructure Supporting the Transition into Motherhood [PDF]

open access: yes, 2019
Copyright © ACM. The transition into motherhood is a complicated and often unsupported major life disruption. To alleviate mental health issues and to support identity re-negotiation, mothers are increasingly turning to online mothers\u27 groups ...
Barkhuus, Louise   +2 more
core   +1 more source

Rare additional chromosomal abnormalities in acute promyelocytic leukaemia resulting in rapidly fatal disease: report of a case

open access: yeseJHaem, 2022
Background Acute promyelocytic leukaemia results from reciprocal translocation between the long arms of chromosomes 15 and 17. This translocation leads to the formation of chimeric gene, which is both the diagnostic marker as well as the therapeutic ...
Ahmed Maseh Haidary   +15 more
doaj   +1 more source

Effectiveness of nurse home-visiting for disadvantaged families: results of a natural experiment [PDF]

open access: yes, 2013
Extent: 9p.Objective: To evaluate the effects of a postnatal home-visiting programme delivered by community health nurses to socially disadvantaged mothers in South Australia.
Bowering, K.   +3 more
core   +2 more sources

The construction of self in relationships: narratives and references to mental states during picture-book reading interactions between mothers and children [PDF]

open access: yes, 2017
Previous studies showed that mothers vary in the way in which they discuss past experiences with their children, since they can exhibit narrative (elaborative) or paradigmatic (repetitive) styles to different extents.
Longobardi, Emiddia   +3 more
core   +2 more sources

Postnatal clinical phenotype of five patients with Pallister–Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature

open access: yesMolecular Genetics & Genomic Medicine, 2019
Background Pallister–Killian syndrome (PKS) is a rare sporadic disorder caused by tetrasomy of the short arm of chromosome 12. The main clinical manifestations are global developmental delay, intellectual disability, epilepsy, dysmorphic features ...
Amerh Salem Alqahtani   +12 more
doaj   +1 more source

Risk factors of breast cancer among patients in a tertiary care hospitals in Afghanistan: a case control study

open access: yesBMC Cancer, 2021
Background Breast cancer is the second most common causes of women’s death, worldwide. Data on risk factors associated with female breast cancer in the Afghan population is very limited. The aim of our study was to identifying risk factor associated with
Zekrullah Baset   +3 more
doaj   +1 more source

The Co-occurrence of child and intimate partner maltreatment in the family: characteristics of the violent perpetrators [PDF]

open access: yes, 2007
This study considers the characteristics associated with mothers and fathers who maltreat their child and each other in comparison to parents who only maltreat their child.
A. E. Appel   +49 more
core   +2 more sources

Reduction of gastroschisis using a surgical glove in the absence of standard silos

open access: yesJournal of Pediatric Surgery Case Reports, 2020
Gastroschisis is a congenital abdominal wall defect with incidence of 1 in 4000 live births. The primary goal of treatment is to reduce bowel back to the abdominal cavity with minimizing risk of injury to the bowel or increased intra-abdominal pressure ...
Mohammad Akbar Shirzad   +3 more
doaj   +1 more source

Giant hamartomatous polyp of the uterine cervix with heterologous mesenchymal tissue in a child: a case report

open access: yesJournal of Medical Case Reports, 2021
Background Polyps of the uterine cervix are one of the most common benign hyperplastic lesions occurring in the female genital tract that usually arise from the endocervical canal and are believed to be the result of reactive changes due to long-standing
Esmatullah Esmat   +5 more
doaj   +1 more source

Ergothioneine supplementation improves pup phenotype and survival in a murine model of spinal muscular atrophy

open access: yesFEBS Letters, EarlyView.
Spinal muscular atrophy (SMA) is a genetic disease affecting motor neurons. Individuals with SMA experience mitochondrial dysfunction and oxidative stress. The aim of the study was to investigate the effect of an antioxidant and neuroprotective substance, ergothioneine (ERGO), on an SMNΔ7 mouse model of SMA.
Francesca Cadile   +8 more
wiley   +1 more source

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