UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Browse by UCL Departments and Centres

Up a level
Export as [feed] RSS 2.0 [feed] RSS 1.0 [feed] Atom
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; Dennett, X; Trounce, I; (1991) Oxidative Energy Failure in Postmitotic Cells - A Major Factor in Senescence. Revue Neurologique , 147 (6-7) 532 - 535.

Byrne, E; JeanFrancois, B; Thyagarajan, D; Collins, S; Dennett, X; 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; Trounce, I; 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; Trounce, I; Marzuki, S; Dennett, X; Berkovic, SF; Davis, S; ... Ozawa, T; + view all (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; White, O; 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; Dennett, X; Byrne, E; 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; Rudduck, C; Marzuki, S; Dennett, X; 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; Byrne, E; (1991) Marinesco-Sjogren syndrome. In: Handbook of Clinical Neurology. (341 - 346). Elsevier Science B.V.: Amsterdam.

F

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

K

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

L

Lomas, DA; Ip, M; Chamba, A; 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; Noer, AS; Lertrit, P; Thyagarajan, D; Kapsa, R; Utthanaphol, P; 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; Noer, AS; Lertrit, P; Ulthanophol, P; Thyagarajan, D; Kapsa, R; ... Byrne, E; + view all (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; Noer, AS; Sudoyo, H; Byrne, E; (1991) Mitochondrial DNA mutations in disease and ageing. Proceedings of the Australian Physiological and Pharmacology Society , 22 152 - 167.

McKelvie, PA; Morley, JB; Byrne, E; 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; Sudoyo, H; Lertrit, P; Thyagarajan, D; Utthanaphol, P; Kapsa, R; ... Marzuki, S; + view all (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; Byrne, E; Roberts, L; Gates, P; (1991) Hemitonic Seizures - Etiologic and Diagnostic Considerations. Acta Neurologica Scandinavica , 84 (1) 59 - 64.

T

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

Trounce, I; Byrne, E; Dennett, X; Chen, WW; 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; Byrne, E; Marzuki, S; Dennett, X; Sudoyo, H; Mastaglia, F; 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 Sun Aug 31 03:14:35 2014 BST.