Author/Creator: Chapple, J P - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Chapple, J P

1. 002 Detecting retinal changes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) using optical coherence tomography (OCT). Issue 3 (9th February 2012)

Authors:: Giunti, P; Nethisinghe, S; Clayton, L M; Vermeer, S; Chapple, J P; Reilly, M M; Bremner, F
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. 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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3. 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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4. The immune cell infiltrate in the tumour microenvironment of phaeochromocytomas and paragangliomas. Issue 11 (19th September 2022)

Authors:: Tufton, N; Hearnden, R J; Berney, D M; Drake, W M; Parvanta, L; Chapple, J P; Akker, S A
Journal:: Endocrine-related cancer
Issue:: Volume 29:Issue 11(2022)
Page Start:: 589
Record Type:: Journal Article
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