Zobrazeno 1 - 10
of 154
pro vyhledávání: '"Edward Byrne"'
Autor:
Clio Berry, Ellisha Othman, Jun Chuen Tan, Brioney Gee, Rory Edward Byrne, Joanne Hodgekins, Daniel Michelson, Alvin Lai Oon Ng, Nigel V. Marsh, Sian Coker, David Fowler
Publikováno v:
BMC Psychiatry, Vol 19, Iss 1, Pp 1-13 (2019)
Abstract Background A social recovery approach to youth mental health focuses on increasing the time spent in valuable and meaningful structured activities, with a view to preventing enduring mental health problems and social disability. In Malaysia,
Externí odkaz:
https://doaj.org/article/3692763fb2ee43bcb86265540fa35dee
Autor:
Edward Byrne, Charles Clarke
More than ever, we need our universities to be engines of change and social justice. Universities can play a major role in making this complex and changing world a better place, helping economies and societies to adapt and respond to the grand challe
Autor:
Anita F. Quigley, Robert M. I. Kapsa, K Steeper, Panos A. Ioannou, Andrew J. Kornberg, Edward Byrne, Jim Vadolas
Publikováno v:
Gene Therapy. 28:470-470
Autor:
Edward Byrne, U. A. Walker
Publikováno v:
Acta Neurologica Scandinavica. 92:273-280
The mitochondrial respiratory chain encephalomyopathies represent an important group of multisystem disorders. No curative treatment is currently available. A number of measures have been reported to have a theoretical potential to improve respirator
Autor:
Katrina Reardon, X. Dennet, Rachael M. Duff, D.R. Williams, Leslie Roberts, Edward Byrne, Nigel G. Laing
Publikováno v:
Neurology. 64:1245-1254
Objective: To report a dominant, slowly progressive early onset distal myopathy with sparing of the tibialis anterior. Methods: Twelve affected and two possibly affected members from an Australian kindred were examined and investigated by EMG, imagin
Autor:
Edward Byrne, Anita F. Quigley, Robert M. I. Kapsa, Sophie Katsabanis, Rosetta Marotta, Judy Chin, Steven J. Collins
Publikováno v:
Internal Medicine Journal. 34:10-19
Background: Many diverse pathogenic mitochondrial DNA (mtDNA) mutations have been described since 1988. The Melbourne Neuromuscular Research Institute (MNRI) has undertaken diagnostic detection of selected mtDNA mutations since 1990. MtDNA mutations
Autor:
Edward Byrne, John B. Kurek, Lawrence Austin, Timothy M. Bennett, Sandra J Feeney, M. J. Bernadette Jean-François, CM Muldoon
Publikováno v:
Cytokine. 23:108-118
Before potential therapeutic strategies for the treatment of amyotrophic lateral sclerosis (ALS) can be advanced to human clinical trials, there is a need to assess them in an animal model that best resembles the disease process. SOD1 G93A mice have
Publikováno v:
The Lancet Neurology. 2:299-310
Summary The development of therapeutic strategies that overcome the unique problems posed by Duchenne muscular dystrophy (DMD) has lead to the development of many contemporary approaches to human disease in general. Various treatment approaches have
Autor:
Edward Byrne
Publikováno v:
Internal Medicine Journal. 33:1-4
Autor:
Edward Byrne
Publikováno v:
Journal of Clinical Neuroscience. 9:497-501
Respiratory chain dysfunction has been established as having a primary pathoaetiological role in certain relatively rare multisystem disorders (typically encephalomyopathies) and postulated as having an important role in commoner neurodegenerative di