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Journal of Pediatric Endocrinology & Metabolism : JPEM|September 22, 2011
Structural chromosome disruption of the NR3C2 gene causing pseudohypoaldosteronism type 1 presenting in infancySusan M O'Connell, Stephanie R Johnson, Barry D Lewis, et al.
Journal of Paediatrics and Child Health|August 13, 2021
Pilot study of universal screening of children and child-parent cascade testing for familial hypercholesterolaemia in AustraliaAndrew C Martin, Amanda J Hooper, Richard Norman, et al.
European Journal of Human Genetics : EJHG|November 18, 2025
Enhancing the detection of familial hypercholesterolaemia in general practice: A model for supporting genetic cascade testing in the communityJing Pang, Wendy Barnett, Jane Purdie, et al.
BMJ Open|March 18, 2018
Role of viral and bacterial pathogens in causing pneumonia among Western Australian children: a case-control study protocolMejbah Uddin Bhuiyan, Thomas L Snelling, Rachel West, et al.
Heart, Lung & Circulation|December 14, 2020
Integrated Guidance for Enhancing the Care of Familial Hypercholesterolaemia in AustraliaGerald F Watts, David R Sullivan, David L Hare, et al.
American Journal of Preventive Cardiology|July 30, 2021
Synopsis of an integrated guidance for enhancing the care of familial hypercholesterolaemia: an Australian perspectiveGerald F Watts, David R Sullivan, David L Hare, et al.
Internal Medicine Journal|May 28, 2021
Essentials of a new clinical practice guidance on familial hypercholesterolaemia for physiciansGerald F Watts, David R Sullivan, David L Hare, et al.
Thorax|October 20, 2018
The contribution of viruses and bacteria to community-acquired pneumonia in vaccinated children: a case-control studyMejbah Uddin Bhuiyan, Thomas L Snelling, Rachel West, et al.
Thorax|January 28, 2021
Assessing the impact of the 13 valent pneumococcal vaccine on childhood empyema in AustraliaRoxanne Strachan, Nusrat Homaira, Sean Beggs, et al.
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