[HTML][HTML] Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia
Autosomal recessive Achromatopsia (ACHM) is a rare inherited disorder associated with
dysfunctional cone photoreceptors resulting in a congenital absence of cone input to visual …
dysfunctional cone photoreceptors resulting in a congenital absence of cone input to visual …
[HTML][HTML] fMRI and gene therapy in adults with CNGB3 mutation
EJ Anderson, TM Dekker, M Farahbakhsh, N Hirji… - Brain Research …, 2024 - Elsevier
Achromatopsia is an inherited retinal disease that affects 1 in 30,000–50,000 individuals
and is characterised by an absence of functioning cone photoreceptors from birth. This …
and is characterised by an absence of functioning cone photoreceptors from birth. This …
Sight restoration in congenitally blind humans does not restore visual brain structure
C Hölig, MJS Guerreiro, S Lingareddy… - Cerebral …, 2023 - academic.oup.com
It is unknown whether impaired brain structure after congenital blindness is reversible if sight
is restored later in life. Using structural magnetic resonance imaging, visual cortical surface …
is restored later in life. Using structural magnetic resonance imaging, visual cortical surface …
[HTML][HTML] Comparative the effect of bisphenol A and bisphenol S on the development and spectral sensitivity of cone photoreceptors in zebrafish larvae (Danio rerio)
L Qiu, P Yu, Q Li, C Wen, H Wang, D Zhao… - Ecotoxicology and …, 2025 - Elsevier
Color vision, which is mediated by cone photoreceptors in vertebrates, is essential for
perceiving the external environment. Bisphenol A (BPA) and its substitute bisphenol S (BPS) …
perceiving the external environment. Bisphenol A (BPA) and its substitute bisphenol S (BPS) …
Assessing the structure of the posterior visual pathway in bilateral macular degeneration
Macular degeneration (MD) embodies a collection of disorders causing a progressive loss of
central vision. Cross-sectional MRI studies have revealed structural changes in the grey and …
central vision. Cross-sectional MRI studies have revealed structural changes in the grey and …
Achromatopsia—Visual Cortex Stability and Plasticity in the Absence of Functional Cones
Purpose: Achromatopsia is a rare inherited disorder rendering retinal cone photoreceptors
nonfunctional. As a consequence, the sizable foveal representation in the visual cortex is …
nonfunctional. As a consequence, the sizable foveal representation in the visual cortex is …
[PDF][PDF] Achromatopsia-limits to visual cortex plasticity in the absence of functional cones
PURPOSE. Achromatopsia is a rare inherited disorder rendering retinal cone
photoreceptors nonfunctional. As a consequence, the sizable foveal representation in the …
photoreceptors nonfunctional. As a consequence, the sizable foveal representation in the …
Vision restoration: Little red booster
AR Wade - Current Biology, 2023 - cell.com
Vision restoration: Little red booster: Current Biology Skip to Main Content Advertisement
Current Biology This journal offers authors two options (open access or subscription) to publish …
Current Biology This journal offers authors two options (open access or subscription) to publish …
Achromatopsie
B Käsmann-Kellner, MB Hoffmann - Die Ophthalmologie, 2023 - Springer
Zusammenfassung Die Achromatopsie oder Stäbchenmonochromasie ist eine kongenitale
autosomal-rezessiv vererbte Netzhautdystrophie, die zu Zapfenfehlfunktion mit verminderter …
autosomal-rezessiv vererbte Netzhautdystrophie, die zu Zapfenfehlfunktion mit verminderter …
Visual Tract Integrity before and after gene therapy in congenital Achromatopsia
A Hillel, A Bick, G Nitzan, E Deena, M Ayelet, B Eyal… - 2024 - researchsquare.com
CNGA3-achromatopsia is a rare hereditary syndrome caused by dysfunction of cone
photoreceptors, resulting in low acuity, photoaversion and complete color blindness. Trials …
photoreceptors, resulting in low acuity, photoaversion and complete color blindness. Trials …