Seyedamirhosein Motamedi

Comorbidities Are Associated With Unfavorable Outcome in Aquaporin‐4 Antibody Positive Neuromyelitis Optica Spectrum Disorders and Myelin Oligodendrocyte Glycoprotein Antibody‐Associated Disease: Exploratory Study From the <scp>CROCTINO</scp> Cohort

Hyperreflective retinal foci are associated with retinal degeneration after optic neuritis in neuromyelitis optica spectrum disorders and multiple sclerosis

Multiscale networks in multiple sclerosis

Predicting disease severity in multiple sclerosis using multimodal data and machine learning

Discrimination of multiple sclerosis using OCT images from two different centers

Diagnostic value of intereye difference metrics for optic neuritis in aquaporin-4 antibody seropositive neuromyelitis optica spectrum disorders

Retinal Changes After Acute and Late Optic Neuritis in Aquaporin-4 Antibody Seropositive NMOSD

Longitudinal Retinal Changes in <scp>MOGAD</scp>

Structure–function correlates of vision loss in neuromyelitis optica spectrum disorders

Intraretinal Layer Segmentation Using Cascaded Compressed U-Nets

Prior optic neuritis detection on peripapillary ring scans using deep learning

Serum glial fibrillary acidic protein correlates with retinal structural damage in aquaporin-4 antibody positive neuromyelitis optica spectrum disorder

Retinal Optical Coherence Tomography in Neuromyelitis Optica

Increased Serum Neurofilament Light and Thin Ganglion Cell–Inner Plexiform Layer Are Additive Risk Factors for Disease Activity in Early Multiple Sclerosis

Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders

Modular deep neural networks for automatic quality control of retinal optical coherence tomography scans

Foveal changes in aquaporin‐4 antibody seropositive neuromyelitis optica spectrum disorder are independent of optic neuritis and not overtly progressive

Lateral geniculate nucleus volume changes after optic neuritis in neuromyelitis optica: A longitudinal study

Altered fovea in AQP4-IgG–seropositive neuromyelitis optica spectrum disorders

Functionally Relevant Maculopathy and Optic Atrophy in Spinocerebellar Ataxia Type 1

Normative Data and Minimally Detectable Change for Inner Retinal Layer Thicknesses Using a Semi-automated OCT Image Segmentation Pipeline

Retinal ganglion cell loss in neuromyelitis optica: a longitudinal study

Temporal visual resolution and disease severity in MS