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Showing 1 to 9 of 9 for “"Heart Defects, Congenital"”.

  1. Cell Migration and Survival Pathways in Cardiac Development and Disease

    The file named "saxenaankur.pdf" is the primary dissertation file. All other files ("*.asf", "*.avi") are supplemental files and may be viewed individually.

    utswmed Repository record for Cell Migration and Survival Pathways in Cardiac Development and Disease (opens in a new tab)

  2. Single-Center Experience of Providing Congenital Heart Surgery to Low- and Middle-Income Countries

    … of this study is to analyze the demographics of congenital heart disease (CHD) patients from over 50 low- and middle-income countries (LMICs) who received care at Frontier Lifeline Hospital (FLL), a specialty cardiac center in Chennai, India, and identify the barriers and limitations they faced. …

    utswmed Repository record for Single-Center Experience of Providing Congenital Heart Surgery to Low- and Middle-Income Countries (opens in a new tab)

  3. Infant Heart Transplant: Perioperative Indicators of Neurocognitive Development

    … per 1000 in the United States are born with a congenital heart defect (Limperopoulos et al, 1999), the primary defect in 57% is hypoplastic left heart syndrome (Johnston, 1991). A fatal disease twenty years ago, survival has jumped from less than 5% to 91% of infants surviving their one-month …

    loma-linda Repository record for Infant Heart Transplant: Perioperative Indicators of Neurocognitive Development (opens in a new tab)

  4. The Role of Gap Junctions in Congenital Diseases of the Heart

    … role in the synchronized contraction of the heart and in embryonic development. Connexin43, the major protein of gap junctions in the heart, is targeted by several protein kinases that regulate myocardial cell-cell coupling. We hypothesized that mutations altering sites critical to this …

    loma-linda Repository record for The Role of Gap Junctions in Congenital Diseases of the Heart (opens in a new tab)

  5. Analysing small-sample-sized methylation data to identify biomarkers for congenital heart defects

    Congenital Heart Defects (CHDs) are the most common type of human congenital anomaly, representing 0.8~1.2% of infants at birth and accounting for over 40% of prenatal deaths. Although the exact aetiology remains a significant challenge, epigenetic modifications, such as Deoxyribonucleic Acid (DNA) …

    edithcowan Repository record for Analysing small-sample-sized methylation data to identify biomarkers for congenital heart defects (opens in a new tab)

  6. Thrombosis in Children

    … the hemostatic system in children subjected to heart surgery. Material and methods: Children with thrombosis (Papers I and II) and children at risk of thrombosis (Papers III and IV) were investigated. In the initial study, 128 children referred for a first thrombotic event were retrospectively …

    lund Repository record for Thrombosis in Children (opens in a new tab)

  7. Integrated approaches to elucidate the genetic architecture of congenital heart defects

    Congenital heart defects (CHD) are structural anomalies affecting the heart, are found in 1% of the population and arise during early stages of embryo development. Without surgical and medical interventions, most of the severe CHD cases would not survive after the first year of life. The improved …

    cambridge Repository record for Integrated approaches to elucidate the genetic architecture of congenital heart defects (opens in a new tab)