P. Moradi

发表

RDH12 retinopathy: novel mutations and phenotypic description

Dorothy A. Thompson, G. Holder, S. Bhattacharya, 2011, Molecular vision.

Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.

Dorothy A. Thompson, P. Sergouniotis, A. Webster, 2011, Investigative ophthalmology & visual science.

Teenagers’ perceptions of blindness related to smoking: a novel message to a vulnerable group

S. Kelly, J. Thornton, R. Harrison, 2007, British Journal of Ophthalmology.

Immunodetection of 11β-Hydroxysteroid Dehydrogenase Type 2 in Human Mineralocorticoid Target Tissues: Evidence for Nuclear Localization.

A. Howie, A. Bradwell, M. Hewison, 1997, Endocrinology.

Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study.

A. Stockman, C. Ripamonti, G. Holder, 2012, Investigative ophthalmology & visual science.

Electrophysiological monitoring in a patient with an optic nerve glioma

G. Holder, A. Robson, G. Rose, 2008, Documenta Ophthalmologica.

Degree, duration, and causes of visual loss in uveitis

P. Murray, O. Durrani, P. Stavrou, 2004, British Journal of Ophthalmology.

Leber Congenital Amaurosis and other autosomal recessive retinal dystrophies: A clinical and molecular genetic study

P. Moradi, 2014 .

Molecular genetics of infantile-onset retinal dystrophies

A. Moore, P. Moradi, A. Moore, 2007, Eye.

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1

Dorothy A. Thompson, G. Holder, P. Sergouniotis, 2010, British Journal of Ophthalmology.

Leber Congenital Amaurosis Associated with AIPL1: Challenges in Ascribing Disease Causation, Clinical Findings, and Implications for Gene Therapy

Dorothy A. Thompson, R. MacLaren, M. Michaelides, 2012, PloS one.

Focus on molecules: retinol dehydrogenase 12 (RDH12).

D. Hunt, A. Moore, D. Mackay, 2008, Experimental eye research.

Focus on molecules: centrosomal protein 290 (CEP290).

A. Moore, M. Cheetham, W. L. Davies, 2011, Experimental eye research.

Novel mutations in MERTK associated with childhood onset rod-cone dystrophy

G. Holder, S. Bhattacharya, F. Alkuraya, 2010, Molecular vision.

Emergency eye colour change

P. Moradi, J. Lochhead, H. Bobat, 2022, Emergency Medicine Journal.

Can patients self‐assess their requirement for cataract surgery?

L. Whitefield, P. Moradi, Nicky Shute, 2006, Journal of cataract and refractive surgery.

Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies

M. Michaelides, A. Webster, A. Moore, 2018, Ophthalmology.

Immunodetection of 11 beta-hydroxysteroid dehydrogenase type 2 in human mineralocorticoid target tissues: evidence for nuclear localization.

A. Howie, A. Bradwell, M. Hewison, 1997, Endocrinology.

Epibulbar Molluscum Contagiosum Lesions in Multiple Myeloma

J. Dart, C. Thaung, M. Bhogal, 2011, Cornea.