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Showing 1 to 7 of 7 for “"Atrial septal defect"”.

  1. The genetics of atrial septal defect and patent foramen ovale

    … heart disease is the most common form of birth defect, affecting approximately 1% of liveborn babies. Secundum atrial septal defect (ASD) is the second most common form of congenital heart disease (CHD). Most cases have no known cause. Chromosomal, syndromal and teratogenic causes account for a …

    unsw Repository record for The genetics of atrial septal defect and patent foramen ovale (opens in a new tab)

  2. Secundum atrial septal defect in the adult. Clinical, haemodynamic and electrophysiological aspects.

    Atrial septal defect (ASD) is the most common congenital heart malformation diagnosed in adult life. In this thesis important clinical, haemodynamic and electrophysiological aspects of ASD in the adult are explored. The diagnostic accuracy of magnetic resonance velocity mapping (MRvm)in calculating …

    lund Repository record for Secundum atrial septal defect in the adult. Clinical, haemodynamic and electrophysiological aspects. (opens in a new tab)

  3. Dreidimensionale Rekonstruktion transösophagealer zweidimensionaler Schnittbilder zur quantitativen Analyse von Vorhofseptumdefekten vom Sekundum-Typ

    … of size and spatial relationships of the atrial septal defects to adjacent cardiac structures, which would be advantageous to those contemplating device closure, is described. The aim was to examine the value of the transesophageal threedimensional echocardiography for this purpose. …

    aachen Repository record for Dreidimensionale Rekonstruktion transösophagealer zweidimensionaler Schnittbilder zur quantitativen Analyse von Vorhofseptumdefekten vom Sekundum-Typ (opens in a new tab)

  4. Identificazione di una variante missenso nel gene RBM10 in una famiglia sarda con disabilità intellettiva X-linked

    … syndrome characterized by Talipes equinovarus, Atrial septal defect, Robin sequence and Persistence of the left superior vena cava and pre- or postnatal lethality in affected males. RBM10 has not been reported in XLID patients until now. Genic intolerance score suggested that RBM10 may be …

    cagliari Repository record for Identificazione di una variante missenso nel gene RBM10 in una famiglia sarda con disabilità intellettiva X-linked (opens in a new tab)

  5. A Search For Genetic Modifiers Responsible For Congenital Heart Disease Variability In The Presence Of Nkx2-5 Haploinsufficiency

    … inbred strain background C57Bl/6 frequently have atrial and ventricular septal defects. The incidences are substantially reduced in the Nkx2-5+/- progeny of first-generation: F1) outcrosses to the strains FVB/N or A/J. Defects recur in the second generation: F2) of the F1xF1 intercross or …

    wustl Repository record for A Search For Genetic Modifiers Responsible For Congenital Heart Disease Variability In The Presence Of Nkx2-5 Haploinsufficiency (opens in a new tab)

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

    … 5 years. Common procedures included ventricular septal defect closure (787; 26%) and atrial septal defect repair (700; 23%). Of the total patients, 2950 cases were assigned a Risk adjustment for congenital heart surgery (RACHS-1) score, of which RACHS-1 categories 2 (1146; 39%) and 3 (1033; 35%) …

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