J. Ainsworth

发表

Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome

Colin A. Johnson, D. Horn, S. Mundlos, 2005, Nature Genetics.

Achromatopsia caused by novel mutations in both CNGA3 and CNGB3

J. Mollon, D. Hunt, M. Michaelides, 2004, Journal of Medical Genetics.

Ectopic expression of the B cell-attracting chemokine BCA-1 (CXCL13) on endothelial cells and within lymphoid follicles contributes to the establishment of germinal center-like structures in Sjögren's syndrome.

M. Salmon, D. Scheel-Toellner, S. Bowman, 2001, Arthritis and rheumatism.

Survey of artificial tear and saliva usage among patients with Sjögren's syndrome

S. Bowman, B. Speculand, J. Ainsworth, 2001, Annals of the rheumatic diseases.

Progressive cone dystrophy associated with mutation in CNGB3.

J. Mollon, D. Hunt, M. Michaelides, 2004, Investigative ophthalmology & visual science.

Isolated Intraocular Relapse of Pediatric B-cell Precursor Acute Lymphoblastic Leukaemia Following Chimeric Antigen Receptor T-lymphocyte Therapy

G. Lucchini, P. Amrolia, J. Ainsworth, 2020, Cureus.

Indications for and Accuracy of Magnetic Resonance Imaging and Computed Tomography in Orbital Disease

D. Hadley, G. Teasdale, P. Macpherson, 1992, Scottish medical journal.

Cataract associated with type-1 diabetes mellitus in the pediatric population.

M. E. Wilson, J. Kivlin, O. Cruz, 2007, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Loss-of-function mutations in RAB18 cause Warburg micro syndrome.

Mark T. Handley, J. Graham, F. Müller, 2011, American journal of human genetics.

Study of p.N247S KERA mutation in a British family with cornea plana.

A. de la Chapelle, S. Tuft, S. Bhattacharya, 2007, Molecular vision.

Follicular thyroid carcinoma metastatic to the iris: a solitary lesion treated with iridocyclectomy.

B. Damato, W. Alexander, W. Lee, 1992, Archives of ophthalmology.

Adjuvant use of laser in eyes with macular retinoblastoma treated with primary intravenous chemotherapy

B. Morland, M. Parulekar, A. Stacey, 2020, British Journal of Ophthalmology.

Flares of systemic disease in primary Sjögren's syndrome.

S. Bowman, J. Ainsworth, J. Hamburger, 2005, Rheumatology.

A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract

D. Hunt, S. Bhattacharya, A. Webster, 2005, Journal of Medical Genetics.

Update from the Ophthalmology Child Abuse Working Party: Royal College Ophthalmologists

R. Doran, P. Luthert, J. Ainsworth, 2004, Eye.

Sucrose and non-nutritive sucking for the relief of pain in screening for retinopathy of prematurity: a randomised controlled trial

N. McIntosh, Y. Freer, J. Ainsworth, 2005, Archives of Disease in Childhood - Fetal and Neonatal Edition.

Community-Based Study of the Association of High Myopia in Children with Ocular and Systemic Disease

B. Gilmartin, N. Logan, J. Ainsworth, 2004, Optometry and vision science : official publication of the American Academy of Optometry.

Associations of high myopia in childhood

J. Ainsworth, J. Marr, Judith Halliwell-Ewen, 2001, Eye.

Which ocular and neurologic conditions cause disparate results in visual acuity scores recorded with visually evoked potential and teller acuity cards?

J R Buncic, C. Westall, J. R. Buncic, 2000, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

The epidemiology of pediatric glaucoma: the Toronto experience.

J. Ainsworth, A. Levin, Robert H. Taylor, 1999, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Pediatric cataract management with variations in surgical technique and aphakic optical correction.

J. Ainsworth, A. Levin, D. Rootman, 1997, Ophthalmology.

SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions

A. Wyatt, J. Crolla, A. Fielder, 2007, British Journal of Ophthalmology.

Follow up of patients with ocular scarring secondary to LOC syndrome treated by amniotic membrane transplantation

S. Shah, J. Ainsworth, J. Moore, 2005, British Journal of Ophthalmology.

Relationship of infantile periocular hemangioma depth to growth and regression pattern.

M. Parulekar, J. Ainsworth, H. Willshaw, 2009, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

A germline mutation in BLOC1S3/reduced pigmentation causes a novel variant of Hermansky-Pudlak syndrome (HPS8).

Colin A. Johnson, S. Watson, R. Trembath, 2006, American journal of human genetics.

WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndrome

P. Yu-Wai-Man, N. Beer, T. Barrett, 2021, Journal of Medical Genetics.

frequency of large gene deletions demonstrating broader phenotype and high SOX2 anophthalmia syndrome: twelve new cases

A. Wyatt, J. Crolla, A. Fielder, 2007 .

Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families.

A. Stockman, G. Holder, M. Michaelides, 2005, Investigative ophthalmology & visual science.

The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56

T. de Ravel, I. Casteels, G. Arno, 2020, Scientific Reports.

Ocular management of harlequin syndrome.

J. Ainsworth, C. N. Chua, 2001, Archives of ophthalmology.