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Open AccessAbstracts of the XLV International Symposium of ISCEV—Hyderabad, India, 25–29 August 2007
Special Edition of Documenta Ophthalmologica
Documenta Ophthalmologica, 2007, Volume 115, Number 1, Pages 15-59
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Anthony G. Robson, Michel Michaelides, Zubin Saihan, Alan C. Bird and Andrew R. Webster, et al.
Documenta Ophthalmologica, 2008, Volume 116, Number 2, Pages 79-89
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Full-field ERG responses recorded with skin electrodes in paediatric patients with retinal dystrophy
S. P. Meredith, M. A. Reddy, L. E. Allen, A. T. Moore and K. Bradshaw
Documenta Ophthalmologica, 2004, Volume 109, Number 1, Pages 57-66
Book Chapter
Childhood Stationary Retinal Dysfunction Syndromes
Michel Michaelides and Anthony Moore
Essentials in Ophthalmology, 2006, Pediatric Ophthalmology, Neuro-Ophthalmology, Genetics, Pages 179-190
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Eleftherios S. Papathanasiou and Savvas S. Papacostas
Documenta Ophthalmologica, 2008, Volume 116, Number 1, Pages 61-73
Book Chapter
Complete and Incomplete Types of CSNB
2006, Electrodiagnosis of Retinal Diseases, 2, Pages 90-113
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ERG variability in X-linked congenital retinoschisis patients with mutations in the
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Documenta Ophthalmologica, 2008, Volume 116, Number 2, Pages 97-109
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Pattern ERG: clinical overview, and some observations on associated fundus autofluorescence imaging in inherited maculopathy
G.E. Holder, A.G. Robson, C.R. Hogg, M. Kurz-Levin and N. Lois, et al.
Documenta Ophthalmologica, 2003, Volume 106, Number 1, Pages 17-23
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Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene
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Human Genetics, 2007, Volume 122, Numbers 3-4, Pages 293-299
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Agnes B. Renner, Ulrich Kellner, Elke Cropp and Michael H. Foerster
Graefe's Archive for Clinical and Experimental Ophthalmology, 2006, Volume 244, Number 11, Pages 1467-1473