Results 131 to 140 of about 396,798 (317)

Effectiveness of an intervention package on the continuum of care among mothers and their knowledge of non-communicable diseases: a cluster randomised controlled trial in Myanmar

open access: yesBMC Public Health
Background Strategies for the continuum of care (CoC) for mothers and newborns have yet to be adequately evaluated in Myanmar. Similarly, the feasibility of integrating non-communicable diseases (NCDs) education into routine maternal, newborn and child ...
Moe Moe Thandar   +7 more
doaj   +1 more source

Postnatal depression: An understanding of Malaysian perspectives

open access: yes, 2014
Background: Postpartum depression (PND) is considered as a significant health problem and gained special attention due to women’s vulnerability during childbearing years, highly associated with suicide and its negative impacts on women, child, family ...
Binti Mohd Arifin, Siti Roshaidai   +2 more
core  

35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT HUWE1 (HECT, UBA, and WWE Domain Containing E3 Ubiquitin Protein Ligase1, OMIM 300697), located at Xp11.22, encodes a ubiquitin ligase that is highly conserved across species. Genetic variants in HUWE1 described in multiple independent studies cause X‐linked intellectual disability, including in the patients identified by Juberg, Marsidi, and ...
Mindy H. Li   +25 more
wiley   +1 more source

Postnatal experiences of women with cardiac conditions: a systematic review and meta-synthesisAJOG Global Reports at a Glance

open access: yesAJOG Global Reports
Objective: The leading cause of maternal mortality in high-income countries is cardiovascular conditions. The highest risk period for women with cardiac conditions is usually the early postnatal phase; however, postnatal care is often under-resourced. We
Jasmine X. Kiley, BS   +7 more
doaj   +1 more source

De Novo Complex Genomic Rearrangement Spanning 2q31.1 in a Proband With Congenital Malformations: Genotype–Phenotype Correlation and Development of a CGR Detection Pipeline

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The 2q31 region is commonly associated with pathogenic alleles of the HOXD cluster leading to various clinical phenotypes related to skeletal development. We present a proband with tetralogy of Fallot and multiple congenital anomalies. Genomic variant screening including an in‐house CGR detection pipeline pairing genome sequencing (GS ...
Katherine Helle   +10 more
wiley   +1 more source

ЧУВСТВИТЕЛЬНОСТЬ КУЛЬТУР МИКРООРГАНИЗМОВ К АНТИБИОТИКАМ ПРИ ПОСЛЕРОДОВОМ ЭНДОМЕТРИТЕ У КОРОВ

open access: yesВетеринарная патология, 2012
The total number of microorganism in 1 ml of uterine contents of cows which are ill with postnatal endometritis exceeds the above among healthy animals by 1,5 times and is presented by the stamms of Staphylococcus, Streptococcus, Escherichia, Proteus ...

doaj  

Contributions of Retinoid Signaling to Autism-like Behaviors Induced by Early Postnatal Lead Exposure in the Mouse Cerebellum

open access: yesCurrent Issues in Molecular Biology
Autism spectrum disorder (ASD) is a group of neurodevelopmental dysfunctions characterized by a heterogeneous etiology that involves gene–environment interactions.
Xiaochun Xia   +7 more
doaj   +1 more source

Treatment of postnatal depression

open access: yesBMJ, 2003
Effective interventions are available, but the condition remains underdiagnosed Major depressive episodes after childbirth are referred to as postnatal depression or, in the United States, as postpartum depression. During the first six months after delivery the prevalence of major depression is estimated at 12-13%.w1 The precise time frame for ...
openaire   +3 more sources

Enhanced AI-Based Methodologies for Detection of Prenatal & Postnatal Depression In Women [PDF]

open access: yes
The introduction of Artificial Intelligence and Machine Learning technologies has been causing a revolutionary change in the field of mental health, especially in prenatal and postpartum depression prediction.
Gopalakrishnan, Abinaya
core   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli   +18 more
wiley   +1 more source

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