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  1. Article

    Open Access

    Correction: An ERG and OCT study of neuronal ceroid lipofuscinosis CLN2 Battens retinopathy

    Dorothy A. Thompson, Siân E. Handley, Robert H. Henderson, Oliver R. Marmoy in Eye (2021)

  2. Article

    Open Access

    An ERG and OCT study of neuronal ceroid lipofuscinosis CLN2 Battens retinopathy

    Late infantile neuronal ceroid lipofuscinosis (CLN2 Batten disease) is a rare, progressive neurodegenerative disease of childhood. The natural history of motor and language regression is used to monitor the ef...

    Dorothy A. Thompson, Siân E. Handley, Robert H. Henderson, Oliver R. Marmoy in Eye (2021)

  3. Article

    Open Access

    What can visual electrophysiology tell about possible visual-field defects in paediatric patients

    Recognising a potential visual-field (VF) defect in paediatric patients might be challenging, especially in children before the age of 5 years and those with developmental delay or intellectual disability. Vis...

    Siân E. Handley, Maja Šuštar, Manca Tekavčič Pompe in Eye (2021)

  4. Article

    Open Access

    Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting

    To describe the trans-occipital asymmetries of pattern and flash visual evoked potentials (VEPs), in an infant with MRI findings of unilateral optic nerve aplasia and hemi-chiasm dysplasia.

    Sian E. Handley, Oliver R. Marmoy, Sri K. Gore, Kshitij Mankad in Documenta Ophthalmologica (2021)

  5. No Access

    Article

    Pattern-onset and OFFset visual evoked potentials in the diagnosis of hemianopic field defects

    Visual evoked potentials (VEPs) assess the function of the visual pathway from the retina to the primary visual cortex. There is much evidence that monocular pattern-reversal and flash VEPs can distinguish dys...

    Oliver R. Marmoy, Sian E. Handley, Dorothy A. Thompson in Documenta Ophthalmologica (2021)

  6. No Access

    Article

    Misaligned foveal morphology and sector retinal dysfunction in AKT1-mosaic Proteus syndrome

    Proteus syndrome arises as a result of a post-zygotic mosaic activating mutation in the AKT1 oncogene, causing a disproportionate overgrowth of affected tissues. A small number of ocular complications have bee...

    Oliver R. Marmoy, Veronica A. Kinsler, Robert H. Henderson in Documenta Ophthalmologica (2021)

  7. Article

    Open Access

    ERGs on the brain: the benefits of simultaneous flash retinal and cortical responses in paediatric cerebral visual impairment

    To highlight the importance of simultaneous flash electroretinogram (ERG) and visual evoked potential (VEP) recording to differentiate a true flash VEP response from an artefact caused by the intrusion of the ...

    Sian E. Handley, Dorothy A. Thompson, Katrina L. Prise in Documenta Ophthalmologica (2018)