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Number of items: 13.
Article
| Byrne, E (1997) Neuromuscular Disorders. Therapeutic Guidelines : Neurology |
| Byrne, E and Blok, R and Kapsa, R and JeanFrancois, B and Ojaimi, J and Siregar, N and Weng, S and Quigley, A and Katsabanis, S (1997) Molecular mechanisms of mitochondrial DNA disease: From cytopathies to ageing. Brain Pathology , 7 (4) 1275 - 1277. |
| Carrell, RW and Lomas, DA (1997) Conformational disease. Lancet , 350 (9071) 134 - 138. 10.1016/S0140-6736(97)02073-4. |
| Gerraty, RP and Gilford, EJ and Byrne, E (1997) Recovery from multiple brain infarcts complicating basilar artery dissection. Journal of Clinical Neuroscience , 4 (1) 77 - 79. |
| Goldring, K and Warner, JA (1997) Cell matrix interactions in asthma. CLIN EXP ALLERGY , 27 (1) 22 - 27. |
| JeanFrancois, MJB and Collins, S and Kotsimbos, N and Dennett, X and Byrne, E (1997) Are mitochondrial DNA deletions causative in chronic progressive external ophthalmoplegia patients? Journal of Clinical Neuroscience , 4 (2) 163 - 168. |
| Kapsa, R and Siregar, N and Quigley, A and Ojaimi, J and Katsabanis, S and Sue, C and Byrne, E (1997) The polymerase chain reaction in the study of mitochondrial genetics. Journal of Biochemical and Biophysical Methods , 36 (1) 31 - 50. |
| Lomas, DA and Caine, N and Wells, FC (1997) Health technology assessment: time for a randomised controlled trial of the role of lung volume reduction surgery in the treatment of emphysema. THORAX , 52 (9) 755 - 756. |
| Lomas, DA and Caine, N and Wells, FC (1997) Health technology assessment: time for a randomised controlled trial of the role of lung volume reduction surgery in the treatment of emphysema. The Lung Volume Reduction Surgery Trial Project Team. Thorax , 52 (9) 755 - 756. |
| Lomas, DA and Elliott, PR and Carrell, RW (1997) Commercial plasma alpha1-antitrypsin (Prolastin) contains a conformationally inactive, latent component. Eur Respir J , 10 (3) 672 - 675. |
| Marzuki, S and Berkovic, SF and Noer, AS and Kapsa, RMI and Kalnins, RM and Byrne, E and Sasmono, T and Sudoyo, H (1997) Developmental genetics of deleted mtDNA in mitochondrial oculomyopathy. Journal of the Neurological Sciences , 145 (2) 155 - 162. |
| Siregar, NC and Jean-Francois, MJB and Blok, RB and Byrne, E (1997) Genotypic and phenotypic changes in mitochondrial cytopathy cell lines with exhaustive in vitro cell proliferation. The FASEB Journal , 11 (9) A1262 - A1262. |
| Sue, CM and Mitchell, P and Crimmins, DS and Moshegov, C and Byrne, E and Morris, JGL (1997) Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation. Neurology , 49 (4) 1013 - 1017. |