Jan Willem R. Pott

International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy

Valério Carelli, Michele Carbonelli, I.F.M. de Coo et al. · Journal of Neuro-Ophthalmology · 2017 · 213 citations · Full text

Ocular Disease, Neurological Disorder, Optic Nerve +22

Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation

Koji Nishiguchi, Michael A. Sandberg, Aart C. Kooijman et al. · Nature · 2003 · 174 citations

Protein Quality Control, Photoreceptor Cell, Signal Transduction +6

De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy

Elena Buena‐Atienza, Klaus Rüther, Britta Baumann et al. · Scientific Reports · 2016 · 36 citations · Full text

Leber’s hereditary optic neuropathy and vitamin B12 deficiency

Jan Willem R. Pott, Kwok H. Wong · Graefe s Archive for Clinical and Experimental Ophthalmology · 2006 · 34 citations

Ocular Disease, Ophthalmology, Genetic Disorder +8

A Girl Without a Chiasm: Electrophysiologic and MRI Evidence for the Absence of Crossing Optic Nerve Fibers in a Girl With a Congenital Nystagmus

Nomdo M. Jansonius, Ton M. van der Vliet, Frans W. Cornelissen et al. · Journal of Neuro-Ophthalmology · 2001 · 34 citations

Mri Evidence, Ophthalmology, Neuroanatomy +12