Results 51 to 60 of about 793,157 (300)
Maternal health and child mortality in rural India [PDF]
In this paper, the effect of maternal health on the under-five mortality has been examined. Third wave of micro-level National Family Health Survey 2005-06 data for rural India is used.
Pandey, Manoj K.
core +4 more sources
Objective ALS2-related disorder involves retrograde degeneration of the upper motor neurons of the pyramidal tracts, among which autosomal recessive Infantile-onset ascending hereditary spastic paralysis (IAHSP) is a rare phenotype.
Qiang Zhang +6 more
doaj +1 more source
Background To reveal the ethnic disparity in the pneumonia-specific mortality rates of children under the age of 5 years (PU5MRs) and provide suggestions regarding priority interventions to reduce preventable under-five-years-of-age deaths.
Min Luo +5 more
doaj +1 more source
Objective: To detect the role of endothelial progenitor cells (EPCs) treated with platelet microparticles (PMPs) in preeclampsia. Methods: EPCs treated with/without PMPs were labeled and injected to PE rats.
Zhenya Fang +4 more
doaj +1 more source
Characteristics and clinical evaluation of X chromosome translocations
Background Individuals with X chromosomal translocations, variable phenotypes, and a high risk of live birth defects are of interest for scientific study.
Ning Huang +8 more
doaj +1 more source
Dissemination activity and impact of maternal and newborn health projects in Ethiopia, India and Nigeria [PDF]
This study aimed to document the key messages, dissemination activities and impacts of selected projects within the Bill & Melinda Gates Foundation Maternal, Neonatal and Child Health strategy portfolio, and consider how these might contribute toward the
Aidelsburger, Monika +4 more
core +3 more sources
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
Background Biallelic pathogenic variants in PIP5K1C (MIM #606,102) lead to lethal congenital contractural syndrome 3 (LCCS3, MIM #611,369), a rare autosomal recessive genetic disorder characterized by small gestational age, severe multiple joint ...
Fang Zhang +7 more
doaj +1 more source
Early risk factors for adolescent antisocial behaviour: an Australian longitudinal study [PDF]
Objective: This investigation utilizes data from an Australian longitudinal study to identify early risk factors for adolescent antisocial behaviour.
Achenbach T M +20 more
core +2 more sources
Safety and Tolerability of Givinostat: Evidence From Real‐World and Clinical Practice
ABSTRACT Objective The aim of our study was to establish the prevalence of adverse events in a real‐world setting in boys living with Duchenne muscular dystrophy (DMD) treated with givinostat as part of an Expanded Access Program (EAP) in Italy. Methods The cohort included 90 ambulant boys, with age when treatment started between 6 and 23 years (mean ...
Marika Pane +19 more
wiley +1 more source

