5 results match your criteria: "University of Melbourne Heidelberg Victoria Australia.[Affiliation]"

Based on the current paradigm, a healthy bone is one with adequate mass without microarchitectural decay. However, these two features may not be sufficient to ensure that a bone is healthy. In addition, components must be correctly assembled and aligned.

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Background Persistent sensorimotor impairments after stroke can negatively impact quality of life. The hippocampus is vulnerable to poststroke secondary degeneration and is involved in sensorimotor behavior but has not been widely studied within the context of poststroke upper-limb sensorimotor impairment. We investigated associations between non-lesioned hippocampal volume and upper limb sensorimotor impairment in people with chronic stroke, hypothesizing that smaller ipsilesional hippocampal volumes would be associated with greater sensorimotor impairment.

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Background Preeclampsia is pregnancy specific, involving significant maternal endothelial dysfunction. Predictive biomarkers are lacking. We evaluated the biomarker potential, expression, and function of PSG7 (pregnancy-specific β-1 glycoprotein 7) and PSG9 (pregnancy-specific β-1 glycoprotein 9) in preeclampsia.

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Background Dilated cardiomyopathy may be heritable but shows extensive genetic heterogeneity. The utility of whole exome sequencing as a first-line genetic test for patients with dilated cardiomyopathy in a contemporary "real-world" setting has not been specifically established. Using whole exome sequencing with rigorous, evidence-based variant interpretation, we aimed to identify the prevalence of a molecular diagnosis in patients with dilated cardiomyopathy in a clinical setting.

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Article Synopsis
  • - The study examined the occurrence, causes, and effectiveness of genetic testing in infants with developmental and epileptic encephalopathies (DEEs) in Tasmania, focusing on those diagnosed between 2011 and 2016 who had experienced seizures before age 2 and other related symptoms.
  • - Among the 16 identified cases, the incidence of infantile DEEs was found to be 0.44 per 1,000 infants per year, with structural causes in 5 cases and genetic factors in 6 cases, using gene panels and whole exome sequencing (WES).
  • - The research highlights that a methodical approach combining clinical imaging and advanced genetic testing significantly improves diagnostic outcomes for infantile DEEs, which can aid in
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