Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Margaret Sahhar"'
Autor:
Janet L. Wale, Louisa Di Pietro, Heather Renton, Margaret Sahhar, Christine Walker, Pamela Williams, Karen Meehan, Elly Lynch, Melissa Martyn, Jane Bell, Ingrid Winship, Clara L. Gaff
Publikováno v:
Research Involvement and Engagement, Vol 7, Iss 1, Pp 1-12 (2021)
Plain English summary Melbourne Genomics Health Alliance was established in 2013 to steer genomics into health care in Victoria, Australia. The Community Advisory Group (CAG) was formed soon after to provide advice and insights from the patient persp
Externí odkaz:
https://doaj.org/article/e35cac675d3741c5aa0728c52e52c7dc
Autor:
Heather Renton, Elly Lynch, Melissa Martyn, Christine Walker, Louisa Di Pietro, Karen Meehan, Clara Gaff, Jane Bell, Janet L Wale, Margaret Sahhar, Ingrid Winship, Pamela Williams
Publikováno v:
Research Involvement and Engagement, Vol 7, Iss 1, Pp 1-12 (2021)
Research Involvement and Engagement
Research Involvement and Engagement
Background The Melbourne Genomics Health Alliance (the Alliance) is a collaboration of leading hospitals, research and academic organisations, supported by its member organisations and the Victorian Government. The Alliance was set up by its members
Publikováno v:
American Journal of Medical Genetics Part A. 170:2895-2904
Chromosomal microarray is an increasingly utilized diagnostic test, particularly in the pediatric setting. However, the clinical significance of copy number variants detected by this technology is not always understood, creating uncertainties in inte
Publikováno v:
Journal of Paediatrics and Child Health. 52:40-46
Aim Spinal muscular atrophy (SMA) type 1 is a relatively common, untreatable and invariably fatal neuromuscular disorder of early childhood. Psychosocial care is vital in management of families affected by this disease. There are few studies examinin
Publikováno v:
Journal of Genetic Counseling. 24:597-607
Indigenous populations are thought to have particularly low levels of access to genetic health services, and cultural issues may be a contributing factor. This article presents the findings of the first study of genetic health service provision to In
Autor:
Ephrat Levy-Lahad, Vicki Petrou, Sari Lieberman, Ivan Macciocca, Sharon Lewis, Margaret Sahhar, Martin B. Delatycki, Helen Curd, Agnes Bankier
Publikováno v:
Journal of Community Genetics. 5:139-146
The Melbourne high school Tay–Sachs disease (TSD) carrier screening program began in 1997. The aim of this study was to assess the outcomes of this screening program among those who had testing more than 5 years ago, to evaluate the long-term impac
Publikováno v:
Birth. 40:52-60
Background Advances in genetic technologies have resulted in the diagnosis during pregnancy of increasing numbers of fetal abnormalities. A few published personal commentaries have indicated that health professionals' interactions with couples at ris
Publikováno v:
Journal of Genetic Counseling. 22:897-901
In 2005 a publication about genetic counseling training in Australia recommended that a 2 year Masters program be established to better equip Australian genetic counselors with increased clinical skills and genetic knowledge (Sahhar et al. Journal of
Autor:
Kirsty Mann, L Hodgkin, Adrienne Sexton, M Kentwell, Jan Hodgson, Margaret Sahhar, J. Taylor, Michael Bogwitz, Y Bylstra
Publikováno v:
Journal of Genetic Counseling. 22:175-187
A model for practising genetic counselors to obtain clinical supervision via reciprocal peer observation and feedback was developed and trialled. The model was developed in response to a perceived lack of opportunity for immediate observational feedb
Publikováno v:
Pacing and Clinical Electrophysiology. 35:62-72
Background: An implantable cardioverter defibrillator (ICD) is a device used in the treatment of individuals with life-threatening cardiac conditions. These include genetic disorders such as long QT syndrome, hypertrophic cardiomyopathy, and Brugada