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

Author/Creator Holder, G E

1. A detailed phenotypic study of "cone dystrophy with supernormal rod ERG". Issue 3 (17th February 2005)

Authors:: Michaelides, M; Holder, G E; Webster, A R; Hunt, D M; Bird, A C; Fitzke, F W; Mollon, J D; Moore, A T
Journal:: British journal of ophthalmology
Issue:: Volume 89:Issue 3(2005)
Page Start:: 332
Record Type:: Journal Article
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2. A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. Issue 2 (21st January 2005)

Authors:: Michaelides, M; Holder, G E; Hunt, D M; Fitzke, F W; Bird, A C; Moore, A T
Journal:: British journal of ophthalmology
Issue:: Volume 89:Issue 2(2005)
Page Start:: 198
Record Type:: Journal Article
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3. ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy. Issue 12 (16th November 2007)

Authors:: Michaelides, M; Chen, L L; Brantley, M A; Andorf, J L; Isaak, E M; Jenkins, S A; Holder, G E; Bird, A C; Stone, E M; Webster, A R
Journal:: British journal of ophthalmology
Issue:: Volume 91:Issue 12(2007)
Page Start:: 1650
Record Type:: Journal Article
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4. Abnormal visual projection in a human albino studied with functional magnetic resonance imaging and visual evoked potentials. Issue 4 (1st April 2002)

Authors:: Morland, A B; Hoffmann, M B; Neveu, M; Holder, G E
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 72:Issue 4(2002)
Page Start:: 523
Record Type:: Journal Article
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5. Acute zonal occult outer retinopathy: towards a set of diagnostic criteria. Issue 1 (21st December 2004)

Authors:: Francis, P J; Marinescu, A; Fitzke, F W; Bird, A C; Holder, G E
Journal:: British journal of ophthalmology
Issue:: Volume 89:Issue 1(2005)
Page Start:: 70
Record Type:: Journal Article
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6. ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing. Issue 9 (8th July 2008)

Authors:: Burgess, R; MacLaren, R E; Davidson, A E; Urquhart, J E; Holder, G E; Robson, A G; Moore, A T; Keefe, R O'; Black, G C M; Manson, F D C
Journal:: Journal of medical genetics
Issue:: Volume 46:Issue 9(2009)
Page Start:: 620
Record Type:: Journal Article
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7. 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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8. An autosomal recessive cone–rod dystrophy associated with amelogenesis imperfecta. Issue 6 (1st June 2004)

Authors:: Michaelides, M; Bloch-Zupan, A; Holder, G E; Hunt, D M; Moore, A T
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 6(2004)
Page Start:: 468
Record Type:: Journal Article
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9. Batten disease: features to facilitate early diagnosis. Issue 9 (5th June 2006)

Authors:: Collins, J; Holder, G E; Herbert, H; Adams, G G W
Journal:: British journal of ophthalmology
Issue:: Volume 90:Issue 9(2006)
Page Start:: 1119
Record Type:: Journal Article
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10. Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance. Issue 2 (28th January 2008)

Authors:: Vaclavik, V; Chakarova, C; Bhattacharya, S S; Robson, A G; Holder, G E; Bird, A C; Webster, A R
Journal:: British journal of ophthalmology
Issue:: Volume 92:Issue 2(2008)
Page Start:: 299
Record Type:: Journal Article
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