Structural Grading of Foveal Hypoplasia Using Spectral-Domain Optical Coherence Tomography

Mervyn G. Thomas, Anil Kumar, Sarim Mohammad, +6

Ophthalmology

Tissue ImagingStructural GradingEngineeringMedical ImagingOphthalmology +6

The Prevalence of Nystagmus: The Leicestershire Nystagmus Survey

Nagini Sarvananthan, Mylvaganam Surendran, E.O. Roberts, +9

Investigative Ophthalmology & Visual Science

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, +40

Nature Genetics

Developmental AnomalyMendelian DisorderGenetic DisorderGeneticsPathogenesis +4

Congenital nystagmus: Randomized, controlled, double‐masked trial of memantine/gabapentin

Rebecca McLean, Frank A. Proudlock, Shery Thomas, +2

Annals of Neurology

Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7

Shery Thomas, Frank A. Proudlock, Nagini Sarvananthan, +16

Brain

Ocular DiseaseFrmd7 MutationPathologyDermatologyNeurology +14

Hyaluronic Acid and its Effect on Postoperative Adhesions in the Rabbit Flexor Tendon

Shery Thomas, Lynne C. Jones, D. S. Hungerford

Clinical Orthopaedics and Related Research

Tissue EngineeringMechanobiologySoft Tissue InjuryEngineeringSoft Tissue Surgery +13

Abnormal retinal development associated with FRMD7 mutations

Mervyn G. Thomas, Moira Crosier, Susan Lindsay, +9

Human Molecular Genetics

Ocular DiseaseDevelopmental BiologyRetinaOphthalmologyAbnormal Retinal Development +10

The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus

Mervyn G. Thomas, Moira Crosier, Susan Lindsay, +16

Brain

Neurological DisorderGeneticsNystagmus DirectionDermatologyIdiopathic Infantile Periodic +16

Clinical and Oculomotor Characteristics of Albinism Compared to<i>FRMD7</i>Associated Infantile Nystagmus

Anil Kumar, Irène Gottlob, Rebecca J. McLean, +3

Investigative Ophthalmology & Visual Science

Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation

Shery Thomas, Mervyn G. Thomas, Caroline Andrews, +6

European Journal of Human Genetics

Ocular DiseaseOphthalmologyNovel Pax6 MutationGlaucomaOcular Pathology +4