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Group by: Author | Type
Jump to: B | C | F | K | L | M | N | O | T
Number of items: 23.

B

Byrne, E (1991) Mitochondrial DNA abnormalities in human disease. Medical Journal of Australia , 154 646 - 647.

Byrne, E (1991) Neurological aspects of xeroderma pigmentosa (De Sanctis-Cacchione Syndrome). In: Handbook of Clinical Neurology. (335 - 340). Elsevier Science B.V.: Amsterdam.

Byrne, E (1991) The chronic fatigue syndrome: a reappraisal and unifying hypothesis. Clinical and Experimental Neurology , 28 128 - 138.

Byrne, E and Dennett, X and Trounce, I (1991) Oxidative Energy Failure in Postmitotic Cells - A Major Factor in Senescence. Revue Neurologique , 147 (6-7) 532 - 535.

Byrne, E and JeanFrancois, B and Thyagarajan, D and Collins, S and Dennett, X and Marzuki, S (1991) Biochemical and Molecular Investigation of Mitochondrial Disease - An Illustrative Case Showing the Value of A Multifaceted Approach. Australian and New Zealand Journal of Medicine , 21 (6) 837 - 843.

Byrne, E and Trounce, I and Dennett, X (1991) Mitochondrial Theory of Senescence - Respiratory-Chain Protein Studies in Human Skeletal-Muscle. Mechanisms of Ageing and Development , 60 (3) 295 - 302.

Byrne, E and Trounce, I and Marzuki, S and Dennett, X and Berkovic, SF and Davis, S and Tanaka, M and Ozawa, T (1991) Functional Respiratory-Chain Studies in Mitochondrial Cytopathies - Support for Mitochondrial-Dna Heteroplasmy in Myoclonus Epilepsy and Ragged Red Fibers (Merrf) Syndrome. Acta Neuropathologica , 81 (3) 318 - 323.

Byrne, E and White, O and Cook, M (1991) Familial Dystonic Choreoathetosis with Myokymia - A Sleep Responsive Disorder. Journal of Neurology, Neurosurgery and Psychiatry , 54 (12) 1090 - 1092.

C

Collins, S and Dennett, X and Byrne, E and Marzuki, S (1991) Chronic Progressive External Ophthalmoplegia in Patients with Large Heteroplasmic Mitochondrial-Dna Deletions - An Immunocytochemical Study. Acta Neuropathologica , 82 (3) 185 - 192.

Collins, S and Rudduck, C and Marzuki, S and Dennett, X and Byrne, E (1991) Mitochondrial Genome Distribution in Histochemically Cytochrome-C Oxidase-Negative Muscle-Fibers in Patients with A Mixture of Deleted and Wild-Type Mitochondrial-Dna. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease , 1097 (4) 309 - 317.

Cook, M and Byrne, E (1991) Marinesco-Sjogren syndrome. In: Handbook of Clinical Neurology. (341 - 346). Elsevier Science B.V.: Amsterdam.

F

Freilich, R and Byrne, E (1991) Assessment of muscle strength, size and architecture using dynamometry and ultrasonography. Advancements in Clinical Neuroscience , 1 13 - 25.

K

Kempster, P and Gates, P and Byrne, E and Wilson, A (1991) Painful Sciatic Neuropathy Following Cardiac-Surgery. Australian and New Zealand Journal of Medicine , 21 (5) 732 - 735.

L

Lomas, DA and Ip, M and Chamba, A and Stockley, RA (1991) The effect of in vitro and in vivo dexamethasone on human neutrophil function. Agents Actions , 33 (3-4) 279 - 285.

M

Marzuki, S and Noer, AS and Lertrit, P and Thyagarajan, D and Kapsa, R and Utthanaphol, P and Byrne, E (1991) Normal Variants of Human Mitochondrial-Dna and Translation Products - the Building of A Reference Data-Base. Human Genetics , 88 (2) 139 - 145.

Marzuki, S and Noer, AS and Lertrit, P and Ulthanophol, P and Thyagarajan, D and Kapsa, R and Sudoyo, H and Byrne, E (1991) Molecular pathology of mitochondrial respiratory disorders: normal nucleotide variants of human mitochondrial genome and mtDNA lesion in MERRF encephalomyopathy. In: Tsako,, (ed.) Progress in Neuropathology. (181 - 193). Raven Press: New York.

Marzuki, S and Noer, AS and Sudoyo, H and Byrne, E (1991) Mitochondrial DNA mutations in disease and ageing. Proceedings of the Australian Physiological and Pharmacology Society , 22 152 - 167.

McKelvie, PA and Morley, JB and Byrne, E and Marzuki, S (1991) Mitochondrial Encephalomyopathies - A Correlation Between Neuropathological Findings and Defects in Mitochondrial-Dna. Journal of the Neurological Sciences , 102 (1) 51 - 60.

N

Noer, AS and Sudoyo, H and Lertrit, P and Thyagarajan, D and Utthanaphol, P and Kapsa, R and Byrne, E and Marzuki, S (1991) A Transfer Rnalys Mutation in the Mtdna Is the Causal Genetic Lesion Underlying Myoclonic Epilepsy and Ragged-Red Fiber (Merrf) Syndrome. The American Journal of Human Genetics , 49 (4) 715 - 722.

O

Oneil, D and Byrne, E and Roberts, L and Gates, P (1991) Hemitonic Seizures - Etiologic and Diagnostic Considerations. Acta Neurologica Scandinavica , 84 (1) 59 - 64.

T

Thyagarajan, D and Byrne, E and Noer, S and Lertrit, P and Utthanophol, P and Kapsa, R and Marzuki, S (1991) Mitochondrial-Dna Sequence-Analysis in Congenital Myotonic-Dystrophy. Annals of Neurology , 30 (5) 724 - 727.

Trounce, I and Byrne, E and Dennett, X and Chen, WW and Marzuki, S (1991) Affinity-Chromatography Isolation of Human Cytochrome-Oxidase and Small-Scale Western Immunoblot Probing of the Enzyme Complex in Mitochondrial Cytopathy Patients. Biochemical Medicine and Metabolic Biology , 46 (1) 17 - 27.

Trounce, I and Byrne, E and Marzuki, S and Dennett, X and Sudoyo, H and Mastaglia, F and Berkovic, SF (1991) Functional Respiratory-Chain Studies in Subjects with Chronic Progressive External Ophthalmoplegia and Large Heteroplasmic Mitochondrial-Dna Deletions. Journal of the Neurological Sciences , 102 (1) 92 - 99.

This list was generated on Wed May 22 06:42:08 2013 BST.