Determinants of birth weight in a low- and middle-income country: Sri Lanka Child Growth Cohort (SLCGC). [PDF]
Wickramasinghe VP +10 more
europepmc +1 more source
The preparation of soluble and stable metal M2+ dications only stabilized by weakly coordinating anions, that is, M[WCA]2 salts, is an emerging field that, beyond its fundamental interest, holds promise in reactivity due to the high electrophilicity of the central M2+ center.
Samuel Dagorne +3 more
wiley +1 more source
The Impact of Maternal Omega-3 Supplementation on Infant Anthropometric Measures and Pregnancy Outcomes: A Systematic Review and Meta-Analysis. [PDF]
Saei Ghare Naz M +3 more
europepmc +1 more source
Abstract Background and Objectives Muscle‐Eye‐Brain disease (MEB) is a dystroglycanopathy that belongs to the congenital muscular dystrophies. Central nervous system manifestations include congenital brain abnormalities, neurodevelopmental delay, and epilepsy, making it a rare but important cause of developmental and epileptic encephalopathy.
Stefania Kalampokini +6 more
wiley +1 more source
Pooled incidence and predictors of infant mortality in low- and middle-income countries using gamma shared frailty model: Insights for achieving the Sustainable Development Goals. [PDF]
Asgedom DK +7 more
europepmc +1 more source
Self‐limited neonatal epilepsy with 2q24.3 duplications: Case series and literature review
Abstract Objective To clarify the phenotypic spectrum associated with duplications involving the 2q24.3 region, which includes a cluster of genes encoding sodium channel subunits (SCN1A, SCN2A, SCN3A, SCN7A, and SCN9A). Methods We reviewed our research database for patients with epilepsy and 2q24.3 duplication and performed thorough phenotyping.
Saba Al Rawahi, Kenneth A. Myers
wiley +1 more source
Impacts of rising food prices on nutritional outcomes and mortality of children in low and middle-income countries: a systematic review. [PDF]
Domun T +6 more
europepmc +1 more source
KCNJ4 variants disrupt inward‐rectifier potassium channel function and cause refractory epilepsy
Abstract Objective Epilepsy is a common neurological disorder with a strong genetic basis, most frequently arising from ion channel dysfunction. Although multiple inwardly rectifying potassium (Kir) channels have been implicated in epileptogenesis, the contribution of KCNJ4, which encodes the Kir2.3 channel, has not previously been established in human
Hu Pan +20 more
wiley +1 more source
Too young to die: social inequalities and infant mortality in marginalized Roma communities in Slovakia. [PDF]
Šprocha B, Bleha B.
europepmc +1 more source

