A. Ionides

发表

Clinical and genetic heterogeneity in autosomal dominant cataract

S. Bhattacharya, A. Moore, P. Francis, 1999 .

Opacification of Array SA40N silicone multifocal intraocular lens.

L. Werner, J. Sheldrick, A. Ionides, 2007, Journal of cataract and refractive surgery.

A. Ionides, 2007 .

National survey of the management of eye emergencies in the accident and emergency departments by senior house officers: 10 years on—has anything changed?

A. Hussain, A. Ionides, D. Sim, 2008, Emergency Medicine Journal.

Pathogenic variants in the CYP21A2 gene cause isolated autosomal dominant congenital posterior polar cataracts

Nikolas Pontikos, M. Michaelides, A. Kalitzeos, 2021, Ophthalmic genetics.

A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q

S. Bhattacharya, A. Moore, A. Ionides, 2011, European Journal of Human Genetics.

Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts

Nikolas Pontikos, M. Michaelides, A. Moore, 2021, Eye.

A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family

V. Plagnol, Nikolas Pontikos, M. Michaelides, 2017, Eye.

Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 gene

S. Bhattacharya, A. Moore, P. Francis, 2005, British Journal of Ophthalmology.

A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.

S. Bhattacharya, A. Moore, D. Mackay, 1997, American journal of human genetics.

Does the ‘Changeover Effect’ Apply to Cataract Surgery Complications?

A. Ionides, Ankur Gupta, 2022, Seminars in ophthalmology.

Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital Cataract

Nikolas Pontikos, M. Michaelides, A. Moore, 2020, Genes.

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin

S. Bhattacharya, P. Francis, S. Khaliq, 1999, Human Genetics.

Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract

Nikolas Pontikos, M. Michaelides, A. Moore, 2018, Eye.

Microbial keratitis following orthokeratology

A. Ionides, T. Poole, O. Frangouli, 2003, Eye.

Cavernous sinus thrombosis secondary to MRSA septicaemia

G. Thompson, A. Ionides, M. Muhtaseb, 2004 .

Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4)

S. Bhattacharya, S. Bhattacharya, A. Moore, 2004, Journal of Medical Genetics.

A system for preoperative stratification of cataract patients according to risk of intraoperative complications: a prospective analysis of 1441 cases

M Muhtaseb, A Kalhoro, A Ionides, 2004, British Journal of Ophthalmology.

Visual outcome following posterior capsule rupture during cataract surgery

S. Tuft, D. Minassian, A. Ionides, 2001, The British journal of ophthalmology.

Visual outcome in patients with isolated autosomal dominant congenital cataract.

S. Bhattacharya, A. Moore, P. Francis, 2001, Ophthalmology.

Screening for ocular surface disease in the intensive care unit

A. Ionides, P. Alexander, A. Kalhoro, 2008, Eye.

A locus for autosomal dominant posterior polar cataract on chromosome 1p.

S. Bhattacharya, A. Moore, D. Mackay, 1997, Human molecular genetics.

A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q.

S. Bhattacharya, S. Bhattacharya, A. Moore, 1998, American journal of human genetics.

Pain perception with pH buffered peribulbar anaesthesia: a pilot study

R. Fernando, A. Ionides, C. Davey, 2000, The British journal of ophthalmology.

Reduced incidence of retinopathy of prematurity

S. Chinn, A. Ionides, E. Rowlands, 2001, The British journal of ophthalmology.

A locus for autosomal dominant anterior polar cataract on chromosome 17p.

S. Bhattacharya, A. Moore, A. Shiels, 1996, Human molecular genetics.

Anterior polar cataract: Clinical spectrum and genetic linkage in a single family

S. Bhattacharya, A. Moore, D. Mackay, 1998, Eye.

Effect of visual acuity on biometry prediction error after cataract surgery

S. Tuft, C. Bunce, A. Ionides, 2003, Journal of cataract and refractive surgery.

Resource management of cataract patients: Can visual rehabilitation be achieved in three visits?

C. Claoué, A. Ionides, 1996, Journal of cataract and refractive surgery.

Toric IOL repositioning

A. Ionides, Ankur Gupta, 2022, International Ophthalmology.

The genetic landscape of crystallins in congenital cataract

Nikolas Pontikos, M. Michaelides, A. Moore, 2020, Orphanet Journal of Rare Diseases.

Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn’s disease in a British family

M. Michaelides, M. Georgiou, R. Quinlan, 2023, BMJ open ophthalmology.

Connexin46 mutations in autosomal dominant congenital cataract.

S. Bhattacharya, S. Bhattacharya, G. Rouleau, 1999, American journal of human genetics.

Internal carotid artery dissection secondary to excessive vocal output

N. Hirji, A. Ionides, 2011, BMJ Case Reports.

Intraoperative complications of cataract surgery in the very old

C. Bunce, W. Xing, S. Robbie, 2006, British Journal of Ophthalmology.

Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract

Nikolas Pontikos, M. Michaelides, M. Cheetham, 2018, Eye.

Visual fields in patients with multifocal intraocular lens implants and monovision: an exploratory study

C. Bunce, M. Wilkins, A. Ionides, 2010, Eye.

Visual outcome following posterior capsule rupture during cataract surgery

S. Tuft, D. Minassian, A. Ionides, 2001, The British journal of ophthalmology.

Moorfields cataract surgery recovery pilot during the Covid-19 pandemic

B. Hussain, V. Maurino, A. Ionides, 2021, Eye.

Does acute suprachoroidal haemorrhage during phacoemulsification cataract surgery need surgical treatment?

A. Ionides, Ankur Gupta, 2022, Graefe's Archive for Clinical and Experimental Ophthalmology.