Hannah Davidson

ORCID: 0000-0002-7348-4355
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About
Contact & Profiles
Research Areas
  • Congenital Heart Disease Studies
  • Cardiac Structural Anomalies and Repair
  • Coronary Artery Anomalies
  • Birth, Development, and Health
  • Cardiovascular and Diving-Related Complications
  • Cardiovascular Conditions and Treatments
  • Aortic Disease and Treatment Approaches
  • Ultrasound in Clinical Applications
  • Genetic Neurodegenerative Diseases
  • Tracheal and airway disorders
  • Kawasaki Disease and Coronary Complications
  • Cardiovascular Issues in Pregnancy

Women and Children’s Health Research Institute
2024

University of Alberta
2024

Children's Hospital at Westmead
2022-2023

The University of Sydney
2022-2023

Women's and Children's Hospital
2021

Information about the prenatal exclusion test for Huntington9s disease (HD) has been given to an unselected series of couples who attended genetic counselling clinic from 1986 onwards. Ten underwent 13 tests during this period with expressed intention stopping a pregnancy if result indicated high risk (almost 50%) that fetus carried HD gene. Nine fetuses at nearly 50% carrying gene were identified but only six such pregnancies terminated. In each three which continued, mother made "final...

10.1136/jmg.32.2.97 article EN Journal of Medical Genetics 1995-02-01

There is increasing demand for accurate early fetal cardiac disease (FCD). We assessed the accuracy of echo (EFE) conducted in our high-volume program and reviewed spectrum FCD, associated genetic anomalies, outcomes encountered.

10.1016/j.echo.2024.08.012 article EN cc-by-nc-nd Journal of the American Society of Echocardiography 2024-08-30

Antegrade pulmonary blood flow (APBF) may be left or eliminated at the time of superior cavopulmonary connection (SCPC). Our aim was to assess impact leaving native APBF SCPC on long-term Fontan outcomes.

10.1016/j.xjon.2023.09.009 article EN cc-by-nc-nd JTCVS Open 2023-09-19

Truncus arteriosus (TA) or persistent arterial trunk describes the presence of a solitary arising from base heart, supported by common ventriculoarterial junction. The gives rise to coronary arteries, systemic and at least one pulmonary artery. is rare congenital cardiac disease, even rarer absence ventricular septal defect.We report case 2-day-old infant who presented with cyanosis murmur. He was diagnosed TA intact septum (IVS), as well crossed arteries which identified on pre-operative...

10.1093/ehjcr/ytad134 article EN cc-by-nc European Heart Journal - Case Reports 2023-03-29

Kawasaki disease (KD) is one of the most common causes acquired cardiac in children high-income countries. The incidence coronary artery (CAD), despite treatment with intravenous immunoglobulin, ranges from 5 to 20%. Determining risk factors for CAD may assist management and reduce long-term complications.Retrospective data were collected all patients presenting Women's Children's Hospital a discharge diagnosis KD over 10.5-year period, 2007 2018.A total 141 included review; 101 fulfilled...

10.1111/jpc.15603 article EN Journal of Paediatrics and Child Health 2021-06-01
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