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Kate Ahmad

Showing results (11-20 of 22) with videos related to

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Practical Neurology|January 10, 2016
A rare cause of weaknessSue-Faye Siow, Hwei-Choo Soh, Alison Lyons, et al.
Annals of Clinical and Translational Neurology|January 9, 2026
Adult-Onset Subacute Sclerosing Panencephalitis Presenting With Subacute Cognitive DeficitsDennis Yeow, Nicola McKern, Vincent Oxenham, et al.
Ophthalmic Genetics|April 10, 2026
Novel heterozygous UCHL1 variant causing severe optic atrophy and vision lossNatalie S Lee, Clare L Fraser, Zornitza Stark, et al.
Neuro-Ophthalmology (Aeolus Press)|June 30, 2026
UCHL1-Related Dominant Optic Atrophy: Report of Two New FamiliesNatalie S Lee, John R Grigg, Zornitza Stark, et al.
Journal of Pediatric Ophthalmology and Strabismus|November 21, 2017
Surgical Technique for Pulled in Two Syndrome: Three Cases With Chronic Progressive External OphthalmoplegiaAlexander Matthew Jones, Julia Starte, Hamish Dunn, et al.
Internal Medicine Journal|November 4, 2024
Sudden-onset ptosis as a presenting feature of thalamic strokeNatalie Si-Yi Lee, Erin Yangyang Xiao, Kate Ahmad, et al.
American Journal of Ophthalmology|June 24, 2020
Bruch's Membrane Opening Minimum Rim Width Provides Objective Differentiation between Glaucoma and Nonglaucomatous Optic NeuropathiesJohn C Leaney, Vuong Nguyen, Eduardo Miranda, et al.
Journal of Movement Disorders|June 1, 2021
Dystonia Responsive to Dopamine: POLG Mutations Should Be Considered If Sensory Neuropathy Is PresentJessica Qiu, Kishore Raj Kumar, Eloise Watson, et al.
Internal Medicine Journal|August 19, 2025
Neurological manifestations of chronic graft versus host diseaseTal Koren, Alice Kwok, William Stevenson, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|July 21, 2023
Mitochondrial DNA 13513G>A Mutation Causing Leber Hereditary Optic Neuropathy Associated With Adult-Onset Renal FailureGrace Swart, Clare L Fraser, Meena Shingde, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Practical Neurology|January 10, 2016
A rare cause of weaknessSue-Faye Siow, Hwei-Choo Soh, Alison Lyons, et al.
Annals of Clinical and Translational Neurology|January 9, 2026
Adult-Onset Subacute Sclerosing Panencephalitis Presenting With Subacute Cognitive DeficitsDennis Yeow, Nicola McKern, Vincent Oxenham, et al.
Ophthalmic Genetics|April 10, 2026
Novel heterozygous UCHL1 variant causing severe optic atrophy and vision lossNatalie S Lee, Clare L Fraser, Zornitza Stark, et al.
Neuro-Ophthalmology (Aeolus Press)|June 30, 2026
UCHL1-Related Dominant Optic Atrophy: Report of Two New FamiliesNatalie S Lee, John R Grigg, Zornitza Stark, et al.
Journal of Pediatric Ophthalmology and Strabismus|November 21, 2017
Surgical Technique for Pulled in Two Syndrome: Three Cases With Chronic Progressive External OphthalmoplegiaAlexander Matthew Jones, Julia Starte, Hamish Dunn, et al.
Internal Medicine Journal|November 4, 2024
Sudden-onset ptosis as a presenting feature of thalamic strokeNatalie Si-Yi Lee, Erin Yangyang Xiao, Kate Ahmad, et al.
American Journal of Ophthalmology|June 24, 2020
Bruch's Membrane Opening Minimum Rim Width Provides Objective Differentiation between Glaucoma and Nonglaucomatous Optic NeuropathiesJohn C Leaney, Vuong Nguyen, Eduardo Miranda, et al.
Journal of Movement Disorders|June 1, 2021
Dystonia Responsive to Dopamine: POLG Mutations Should Be Considered If Sensory Neuropathy Is PresentJessica Qiu, Kishore Raj Kumar, Eloise Watson, et al.
Internal Medicine Journal|August 19, 2025
Neurological manifestations of chronic graft versus host diseaseTal Koren, Alice Kwok, William Stevenson, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|July 21, 2023
Mitochondrial DNA 13513G>A Mutation Causing Leber Hereditary Optic Neuropathy Associated With Adult-Onset Renal FailureGrace Swart, Clare L Fraser, Meena Shingde, et al.
Pageof 3