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Joint attention and parent-child book readingGood language development is an integral component of school readiness and academic achievement.
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Clinical investigation of respiratory system admittance in preschool childrenWe compared the ability of Ars, to standard oscillatory outcomes, to determine respiratory disease and differentiate responses to inhaled bronchial challenges.
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Severity and persistence of asthma and mental health: a birth cohort studyThe goal of the current study was to investigate asthma and mental health among youth in the community.
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Seasonal variation in fetal growth: Accounting for sociodemographic, biological, and environmental exposuresWe sought to investigate seasonal variation in fetal growth, accounting for important sociodemographic, biological, and environmental exposures.
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Social Gradients in Indigenous HealthThe pattern of association between socioeconomic factors and health outcomes has primarily depicted better health for those who are higher in the social...
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Where were those rabbits? A new paradigm to determine cerebral lateralisation of visuospatial memory function in childrenIn the majority of people, functional differences are observed between the two cerebral hemispheres: language production is typically subserved by the left...
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Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handlingAnkylosing spondylitis is a common form of inflammatory arthritis predominantly affecting the spine and pelvis that occurs in approximately 5 out of 1,000 adult
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Air Trapping on Chest CT Is Associated with Worse Ventilation Distribution in Infants with Cystic FibrosisIn school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is associated with abnormal ventilation distribution.
Using information from the Australian Rett Syndrome database, we coded symptoms according to severity scales and grouped by type and location of mutation.
Therefore, we wanted to compare the features of girls and women with a C-terminal deletion with those with other MECP2 mutations.