Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Georgina Loughnan"'
Autor:
Tanzil Rujeedawa, Nora McNairney, Shelly Cordner, James O’Brien, Georgina Loughnan, Anthony Holland
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-8 (2022)
Abstract Background People with rare disorders face significant global health inequalities; the challenge is how to raise awareness and develop a nucleus of experts in a country who are then able to provide guidance to others in that country. The Int
Externí odkaz:
https://doaj.org/article/c82e34eb00294168bfb31ec6855075fd
Autor:
Kim L Bennell, Nicholas F Taylor, Nora Shields, David Levitt, Jennifer J Watts, Luke Prendergast, Joseph Proietto, Lauren J Rice, Zoë McCallum, Alesha Southby, Tania Markovic, Christine Bigby, Cara Schofield, Georgina Loughnan, Janet Franklin, Viral Chikani, Susan Blair
Publikováno v:
BMJ Open, Vol 12, Iss 12 (2022)
Introduction Preliminary evidence suggests that progressive resistance training may be beneficial for people with Prader-Willi Syndrome (PWS), a rare genetic condition that results in muscle weakness and low muscle tone.To establish whether community
Externí odkaz:
https://doaj.org/article/6f7bddf066d840f29578684277739502
Autor:
Richard C. Franklin, Janet L. Franklin, Jessica M. Swinbourne, Elisia Manson, Georgina Loughnan, Tania Markovic, Samantha Hocking
Publikováno v:
Australian and New Zealand Journal of Public Health. 47:100008
Autor:
Nora Shields, Kim L Bennell, Alesha Southby, Lauren J Rice, Tania Markovic, Christine Bigby, Luke Prendergast, Jennifer J Watts, Cara Schofield, Georgina Loughnan, Janet Franklin, David Levitt, Viral Chikani, Zoe McCallum, Susan Blair, Joseph Proietto, Nicholas F Taylor
Publikováno v:
BMJ Open. 12:e060306
IntroductionPreliminary evidence suggests that progressive resistance training may be beneficial for people with Prader-Willi Syndrome (PWS), a rare genetic condition that results in muscle weakness and low muscle tone.To establish whether community-
Autor:
Amanda Sainsbury, Lesley V. Campbell, Katharine Steinbeck, Herbert Herzog, Georgina Loughnan, Lisa Sze, Alexander Viardot, Louise Purtell, Arabella Smith
Publikováno v:
Obesity. 23:1159-1165
Objective Individuals with Prader–Willi syndrome (PWS) are commonly restricted to 60-75% of height-appropriate calorie intake because they rapidly become obese on a normal diet. This study measured changes in energy expenditure, glucose and lipid h
Autor:
Georgina Loughnan, Arabella Smith, Katharine Steinbeck, A. B. Jenkins, Herbert Herzog, Alexander Viardot, Lisa Sze, Amanda Sainsbury, Lesley V. Campbell, Louise Purtell
Publikováno v:
Clinical Endocrinology. 79:128-133
SummaryContext Individuals with Prader–Willi syndrome (PWS) have a high cardiovascular risk, the mechanism of which is unclear. There may be dysfunction in the autonomic nervous system (ANS) in PWS. Objective To measure, as indicators of cardiac au
Autor:
Louise, Purtell, Alexander, Viardot, Lisa, Sze, Georgina, Loughnan, Katharine, Steinbeck, Amanda, Sainsbury, Herbert, Herzog, Arabella, Smith, Lesley V, Campbell
Publikováno v:
Obesity (Silver Spring, Md.). 24(8)
Autor:
Jason A. Harmer, Michael R. Skilton, David S. Celermajer, Janet Franklin, Ian D. Caterson, David R. Sullivan, Georgina Loughnan, Shirley Nakhla, Daniel P Sieveking
Publikováno v:
Diabetes, Obesity and Metabolism. 10:874-884
Aims: The mechanisms by which obesity confers increased cardiovascular risk and the effects of moderate weight loss on cardiovascular health are incompletely understood. We sought to characterize the preclinical changes in cardiac and vascular health
Autor:
Brendon J. Yee, Craig L. Phillips, Georgina Loughnan, Dev Banerjee, Peter Liu, Ronald R. Grunstein, Kate Steinbeck, Sri Mahadev, Peter R. Buchanan
Publikováno v:
Journal of Clinical Sleep Medicine. :713-718
Objectives:Prader-Willi syndrome (PWS) is a genetic disorder (linked to chromosome 15q11-13) characterized by hypotonia and developmental delay, hyperphagia and obesity, hypersomnia and abnormal sl...
Autor:
David S. Celermajer, Georgina Loughnan, Katharine Steinbeck, Sanjay Patel, Jason A. Harmer, Michael R. Skilton
Publikováno v:
Clinical Endocrinology. 66:771-777
Summary Objective Prader–Willi syndrome (PWS) is a genetic obesity syndrome characterized by hyperphagia, behavioural disturbance and intellectual disability. PWS appears to be associated with a high incidence of sudden death, suspected to be cardi