V. Sheth

发表

Detection and characterisation of optic nerve and retinal changes in primary congenital glaucoma using hand-held optical coherence tomography

I. Gottlob, A. Pilat, Sonal Shah, 2019, BMJ Open Ophthalmology.

Potential of handheld optical coherence tomography to determine cause of infantile nystagmus in children by using foveal morphology.

Mervyn G. Thomas, I. Gottlob, M. Michaelides, 2013, Ophthalmology.

Abnormal retinal development associated with FRMD7 mutations

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

In Vivo Morphology of the Optic Nerve and Retina in Patients With Parkinson's Disease.

I. Gottlob, R. McLean, Y. Rajabally, 2016, Investigative ophthalmology & visual science.

Kostadin Damevski, V. Sheth, 2022, Automated Software Engineering.

Retinal development in infants and young children with albinism: evidence for plasticity in early childhood.

Mervyn G. Thomas, I. Gottlob, R. McLean, 2022, American journal of ophthalmology.

Retinal Development in Infants and Young Children with Achromatopsia

I. Gottlob, M. Michaelides, R. McLean, 2015, Ophthalmology.

Hand‐held optical coherence tomography imaging in children with anterior segment dysgenesis

I. Gottlob, A. Pilat, V. Sheth, 2016, Acta ophthalmologica.

Characterization of Abnormal Optic Nerve Head Morphology in Albinism Using Optical Coherence Tomography.

I. Gottlob, Helena Lee, Sarim Mohammad, 2015, Investigative ophthalmology & visual science.

Development and clinical utility of a novel diagnostic nystagmus gene panel using targeted next-generation sequencing

Mervyn G. Thomas, I. Gottlob, R. McLean, 2017, European Journal of Human Genetics.

Diagnostic potential of iris cross-sectional imaging in albinism using optical coherence tomography.

I. Gottlob, R. McLean, Anil Kumar, 2013, Ophthalmology.

The functional significance of foveal abnormalities in albinism measured using spectral-domain optical coherence tomography.

F. Proudlock, I. Gottlob, Anil Kumar, 2011, Ophthalmology.

Phenotypic features of the visual system in albinism

V. Sheth, 2018 .

Abnormal foveal morphology in carriers of oculocutaneous albinism

I. Gottlob, R. McLean, V. Sheth, 2022, The British journal of ophthalmology.

Management of nystagmus in children: a review of the literature and current practice in UK specialist services

I. Gottlob, F. Shawkat, R. McLean, 2020, Eye.

Aberrant visual pathway development in albinism: From retina to cortex

Thomas Welton, Irene Gottlob, Paul S Morgan, 2018, Human brain mapping.

Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia

Mervyn G. Thomas, I. Gottlob, R. McLean, 2012, British Journal of Ophthalmology.

Longitudinal Evaluation of Changes in Retinal Architecture Using Optical Coherence Tomography in Achromatopsia

Irene Gottlob, Mervyn G. Thomas, Susanne Kohl, 2018, Investigative ophthalmology & visual science.

A COMPARATIVE STUDY OF INJECTABLE IRON-SUCROSE VERSUS ORAL IRON IN POSTPARTUM MODERATE ANEMIA PATIENTS

V. Sheth, R. Patange, 2014 .

Cerebral malaria: insight into pathology from optical coherence tomography

S. Harding, N. Beare, I. Gottlob, 2020, Scientific Reports.

A Rare Case of Massive Ovarian Mucinous Cystadenoma with Vesicovaginal Fistula- An Interesting Case Report

V. Sheth, S. Patil, Yamini Patil, 2014 .

The role of glucocorticoid pulse therapy in pulmonary involvement in leptospirosis.

V. Sheth, P. Wadia, S. Trivedi, 2001, The Journal of the Association of Physicians of India.

Retinal and optic nerve changes in microcephaly

I. Gottlob, E. Papageorgiou, P. Vasudevan, 2018, Neurology.

Retinal and optic nerve changes in microcephaly An optical coherence tomography study

I. Gottlob, E. Papageorgiou, P. Vasudevan, 2022 .

Assessment of the anterior segment of patients with primary congenital glaucoma using handheld optical coherence tomography

I. Gottlob, A. Pilat, Sonal Shah, 2019, Eye.

Optic Nerve Head Development in Healthy Infants and Children Using Handheld Spectral-Domain Optical Coherence Tomography

I. Gottlob, R. McLean, E. Papageorgiou, 2016, Ophthalmology.

In Vivo Foveal Development Using Optical Coherence Tomography.

I. Gottlob, R. McLean, E. Papageorgiou, 2015, Investigative ophthalmology & visual science.

Discordant phenotypes in twins with infantile nystagmus

Mervyn G. Thomas, I. Gottlob, R. McLean, 2021, Scientific Reports.

Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant

I. Gottlob, E. Engle, R. Dineen, 2019, British Journal of Ophthalmology.

Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles

B. Al-Diri, I. Gottlob, E. Engle, 2021, International journal of molecular sciences.

Retinal development in albinism: a prospective study using optical coherence tomography in infants and young children

I. Gottlob, R. McLean, E. Papageorgiou, 2015, The Lancet.

SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization

Mervyn G. Thomas, I. Gottlob, R. McLean, 2020, Human molecular genetics.

Characterization of Abnormal Optic Nerve Head Morphology in Albinism Using Optical Coherence Tomography.

I. Gottlob, Helena Lee, Sarim Mohammad, 2015, Investigative ophthalmology & visual science.

ERG Responses in Albinism, Idiopathic Infantile Nystagmus, and Controls

Mervyn G. Thomas, F. Proudlock, R. McLean, 2024, Investigative ophthalmology & visual science.