Refraction in childhood.

Moore At
Transactions of the ophthalmological societies of the United Kingdom 104 ( 6) 648 -652

6
1985
2
1963
Four Novel 'Protein Truncating' Mutations in the Dynamin–Central Region of Opa1 Causing Autosomal Dominant Optic Atrophy: Structural Model and Functional Consequences

V. Davies , M. Votruba , M. Votruba , M. Sarros
Investigative Ophthalmology & Visual Science 47 ( 13) 4613 -4613

2006
A Survey of Molecular Pathology of 175 Families With Dominant Retinitis Pigmentosa

S. Devery , T. Colclough , G. Wright , A. Moore
Investigative Ophthalmology & Visual Science 50 ( 13) 2297 -2297

2009
A Large Dominant Optic Atrophy Family with a Severe Phenotype Excludes the OPA1 and OPA4 Loci: Evidence of Further Genetic Heterogeneity

D. Thiselton , S. Aijaz , M. Votruba , A. Moore
Investigative Ophthalmology & Visual Science 44 ( 13) 632 -632

2003
ERG responses to full–field stimuli recorded with skin and corneal electrodes in healthy volunteers and in children with retinal dystrophies.

A. Fulton , R. Hansen , S.P. Meredith , K. Bradshaw
Investigative Ophthalmology & Visual Science 45 ( 13) 801 -801

2004
A CRYGD mutation is associated with familial coralliform cataract

A. Moore , A. Moore , A. Ionides , A. Reddy
Investigative Ophthalmology & Visual Science 45 ( 13) 374 -374

2004
Tensile deformation modes in polycrystalline beryllium near the ductile-brittle transition

W. Taylor , A. Moore
Journal of Nuclear Materials 13 ( 1) 23 -27

11
1964
Liver transplantation in a Jehovah’s Witness with ankylosing spondylitis

C. Baldry , S. B. Backman , P. Metrakos , J. Tchervenko
Canadian Journal of Anaesthesia-journal Canadien D Anesthesie 47 ( 7) 642 -646

16
2000
Functional impairment of lens aquaporin in two families with dominantly inherited cataracts

P. Francis , J.-J. Chung , M. Yasui , V. Berry
Human Molecular Genetics 9 ( 15) 2329 -2334

114
2000
Hollow-cathode chemical vapor deposition of thick, low-stress diamond-like carbon films

C. Wasz , S.O. Kucheyev , S. Elhadj , S. Falabella
Thin Solid Films 714 138394

2
2020
Cortical visual processing in patients with congenital achromatopsia: coherent form, motion and biological motion perception

E. Burton , J. Wattam-Bell , K. Nishiguchi , V. Sundaram
Journal of Vision 13 ( 9) 21 -21

1
2013
Clinical and genetic heterogeneity in autosomal dominant cataract

A. Ionides , P. Francis , V. Berry , D. Mackay
British Journal of Ophthalmology 83 ( 7) 802 -808

87
1999
OPA1 gene mutations cluster in functional protein domains in ADOA patients and reveal a founder allele in the Danish population.

D. L. Thiselton , S. Andreasson , C. Alexander , A. T. Moore
INVEST OPHTH VIS SCI , 42 (4) S649 - S649. (2001) 42 ( 4) 649

5
2001
Evaluating the Photoreceptor Mosaic in Blue Cone Monochromacy (BCM)

L. Mizrahi-Meissonnier , E. Banin , A. Dubra , D. M. Hunt
Investigative Ophthalmology & Visual Science 51 ( 13) 2935 -2935

3
2010
A Family With Vitelliform Macular Lesions and Angle-Closure Glaucoma

F. Manson , F. Manson , A. T. Moore , P. T. Khaw
Investigative Ophthalmology & Visual Science 50 ( 13) 4108 -4108

2009
A Molecular Genetic Investigation of Two Families With Macular Dysplasia in Association With Digit Abnormalities

D. M. Hunt , A. T. Moore , A. T. Moore , A. R. Webster
Investigative Ophthalmology & Visual Science 49 ( 13) 456 -456

3
2008