Shery Thomas

发表

Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?

Mervyn G. Thomas, F. Proudlock, I. Gottlob, 2011, Ophthalmology.

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

M. Stratton, P. Futreal, R. Wooster, 2006, Nature Genetics.

The prevalence of nystagmus: the Leicestershire nystagmus survey.

J. Thompson, F. Proudlock, I. Gottlob, 2009, Investigative ophthalmology & visual science.

Phenotyping and genotyping of idiopathic infantile nystagmus

Shery Thomas, 2010 .

Abnormal retinal development associated with FRMD7 mutations

Mervyn G. Thomas, I. Gottlob, M. Crosier, 2014, Human molecular genetics.

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

Mervyn G. Thomas, F. Proudlock, I. Gottlob, 2013, European Journal of Human Genetics.

FRMD7-Related Infantile Nystagmus

Mervyn G. Thomas, F. Proudlock, I. Gottlob, 2011 .

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

Irene Gottlob, A. S. Anil Kumar, Andrea Langmann, 2008, Brain : a journal of neurology.

Erratum: Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography: A predictor of visual acuity? (Ophthalmology (2011) 118 (1653-1160))

F. Proudlock, I. Gottlob, E. Engle, 2011 .

Clinical and oculomotor characteristics of albinism compared to FRMD7 associated infantile nystagmus.

Irene Gottlob, Mervyn G. Thomas, Shery Thomas, 2011, Investigative ophthalmology & visual science.

Optic nerve sheath fenestration for intracranial hypertension associated with chronic inflammatory demyelinating polyneuropathy.

M. Lawden, Shery Thomas, R. Sampath, 2004, Ophthalmic plastic and reconstructive surgery.

Orbital infantile haemangioma: radiological features and treatment – case series and literature review

Shery Thomas, J. Ravenscroft, T. Taylor, 2018, Orbit.

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

Irene Gottlob, Shery Thomas, Frank A. Proudlock, 2007, Annals of neurology.

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

Mervyn G. Thomas, R. Hertle, P. Tarpey, 2011, Brain : a journal of neurology.

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

M. Stratton, P. Futreal, R. Wooster, 2011, Nature Genetics.

Xanthogranulomatous disease in the lacrimal gland

F. Proudlock, I. Gottlob, Shery Thomas, 2005, British Journal of Ophthalmology.

Treatment of acquired periodic alternating nystagmus with memantine: a case report.

F. Proudlock, I. Gottlob, R. McLean, 2009, Clinical neuropharmacology.

The prevalence of nystagmus: the Leicestershire nystagmus survey.

J. Thompson, F. Proudlock, I. Gottlob, 2009, Investigative ophthalmology & visual science.

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

P. Tarpey, F. Proudlock, I. Gottlob, 2008, Brain : a journal of neurology.

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

Mervyn G. Thomas, R. Hertle, P. Tarpey, 2011, Brain : a journal of neurology.

A case of Phoma fungal keratitis in a contact lens user

Shery Thomas, J. Prydal, D. Jenkins, 2015, JRSM open.