Author/Creator: Cheetham, M E - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Cheetham, M E

1. 167 An in-vitro study of distal hereditary motor neuropathy due to homozygous HSJ1 mutations. Issue 3 (9th February 2012)

Authors:: Rossor, A; Kalmar, B; Gray, A; Mustill, W; Schiavo, G; Cheetham, M E; Reilly, M M; Greensmith, L; Novoselov, S
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83:Issue 3(2012)
Page Start:: e1
Record Type:: Journal Article
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2. A laboratory running test: metabolic responses of sprint and endurance trained athletes. Issue 2 (June 1985)

Authors:: Cheetham, M E; Williams, C; Lakomy, H K
Journal:: British journal of sports medicine
Issue:: Volume 19:Issue 2(1985)
Page Start:: 81
Record Type:: Journal Article
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3. An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene. Issue 4 (18th March 2004)

Authors:: Dandekar, S S; Ebenezer, N D; Grayson, C; Chapple, J P; Egan, C A; Holder, G E; Jenkins, S A; Fitzke, F W; Cheetham, M E; Webster, A R; Hardcastle, A J
Journal:: British journal of ophthalmology
Issue:: Volume 88:Issue 4(2004)
Page Start:: 528
Record Type:: Journal Article
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4. High intensity training and treadmill sprint performance. Issue 2 (June 1987)

Authors:: Cheetham, M E; Williams, C
Journal:: British journal of sports medicine
Issue:: Volume 21:Issue 2(1987)
Page Start:: 14
Record Type:: Journal Article
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5. In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patients. Issue 1 (1st January 2002)

Authors:: Grayson, C; Chapple, J P; Willison, K R; Webster, A R; Hardcastle, A J; Cheetham, M E
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 1(2002)
Page Start:: 62
Record Type:: Journal Article
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6. Minimising the risk of prion transmission by contact tonometry. Issue 11 (10th November 2003)

Authors:: Amin, S Z; Smith, L; Luthert, P J; Cheetham, M E; Buckley, R J
Journal:: British journal of ophthalmology
Issue:: Volume 87:Issue 11(2003)
Page Start:: 1360
Record Type:: Journal Article
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7. RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections. Issue 8 (14th August 2003)

Authors:: Zito, I; Downes, S M; Patel, R J; Cheetham, M E; Ebenezer, N D; Jenkins, S A; Bhattacharya, S S; Webster, A R; Holder, G E; Bird, A C; Bamiou, D E; Hardcastle, A J
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 8(2003)
Page Start:: 609
Record Type:: Journal Article
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