Items where authors include "Kuht, H.J."

Article

Sekhri, R., Kuht, H.J., Tu, Z. et al. (15 more authors) (2025) Identifying biomarkers for papilledema and pseudopapilledema. Scientific Reports, 15. 24847. ISSN 2045-2322

Shenoy, R. orcid.org/0000-0001-8118-9009, Maconachie, G.D.E. orcid.org/0000-0001-9131-3480, Parida, S. et al. (19 more authors) (2025) Foveal hypoplasia grading with optical coherence tomography: agreement and challenges across experience levels. Diagnostics, 15 (6). 763. ISSN 2075-4418

Kuht, H.J., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480, Han, J. et al. (36 more authors) (2022) Genotypic and phenotypic spectrum of foveal hypoplasia : a multicenter study. Ophthalmology, 129 (6). pp. 708-718. ISSN 0161-6420

Thomas, M.G., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480, Kuht, H.J. et al. (10 more authors) (2021) Optic nerve head and retinal abnormalities associated with congenital fibrosis of the extraocular muscles. International Journal of Molecular Sciences, 22 (5). 2575.

Kuht, H.J., Han, J., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480 et al. (12 more authors) (2020) SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization. Human Molecular Genetics, 29 (18). pp. 2989-3002. ISSN 0964-6906