Results 101 to 110 of about 11,979,308 (286)

Health Benefits of Walking School Buses in Auckland, New Zealand: Perceptions of Children and Adults

open access: yes, 2006
A modest literature has documented ways that walking school buses (WSBs) can restore walking to and from school as an everyday activity for children. WSBs involve adult volunteers who, as “drivers,” chaperone groups of children walking on the “school run”
Neuwelt, Patricia, Kearns, Robin
core  

School-Based Deworming Program Yields Small Improvement in Growth of Zanzibari School Children After one Year. [PDF]

open access: yes, 1997
Efficacy trials of antihelminthic therapies conducted in Africa have reported improvements in children's growth, but nutritional evaluations of large-scale deworming programs are lacking.
Tielsch, James M.   +14 more
core   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
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

Refractive error and visual impairment in primary school children in Onitsha, Anambra State, Nigeria

open access: yesAfrican Vision and Eye Health, 2018
Background: Vision problems have been shown to adversely affect a child’s achievement in school. Aim: To determine the prevalence of refractive error and visual impairment in primary school children in Onitsha, Anambra State, Nigeria.
Ngozika E. Ezinne   +1 more
doaj   +1 more source

Ofatumumab in Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease: A Comparison With Rituximab

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To evaluate the efficacy and safety of ofatumumab in patients with myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD), and compare it with rituximab. Methods We conducted a single–center, observational study including 22 MOGAD patients treated with ofatumumab and 21 treated with rituximab.
Yuxin Fan   +5 more
wiley   +1 more source

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach   +23 more
wiley   +1 more source

FEATURES OF PHYSICAL DEVELOPMENT OF THE PRIMARY SCHOOLCHILDREN WHO ARE STUDYING IN SCHOOLS OF DIFFERENT TYPES

open access: yesActa Biomedica Scientifica, 2013
Risk factors during the school period are continuous, systematic and long. Even the most minimum influences have their ability to be accumulate and are accompanied by violations of somatic, mental, physical and reproductive health.
E. A. Tkachuk, N. N. Martynovich
doaj  

Vision screening of school children in greenland 2017-2022: coverage and low vision prevalence

open access: yesInternational Journal of Circumpolar Health
Vision screening during childhood is vital for the early detection and treatment of visual impairment that may significantly impact a child’s development and quality of life.
Nick Duelund   +5 more
doaj   +1 more source

Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos   +5 more
wiley   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian   +8 more
wiley   +1 more source

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