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Journal Articles (5)
Meeting Abstract (3)

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Investigative Ophthalmology & Visual Science (8)

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Biochemistry and Molecular Biology (4)
ARVO Annual Meeting Abstract (3)
Articles (1)

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Biochemistry and Molecular Biology (4)
Genetics (4)
Eye Anatomy and Disorders (2)
Cornea (1)
Retina (1)

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autosomal recessive inheritance (3)
chromosomes (3)
family (3)
mutation (3)
dna (2)
adult (1)
conjunctiva (1)
exanthema (1)
genes (1)
keratoconus (1)

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ARVO Annual Meeting Abstract June 2015

Demodex infestation in patients with blepharitis unresponsive to conventional therapy

Christine Purslow; Dimple Patel; E Sykakis; C Williams; M Payne; Francisco C Figueiredo

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4489. doi:

ARVO Annual Meeting Abstract April 2009

Nanomechanical Probes of Individual Corneal Epithelial Cells

S. S. Perry; F. T. Limpoco; J. M. Payne; N. V. Dolgova; B. G. Keselowsky; W. G. Sawyer; H. Ketelson; D. Meadows

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):1765. doi:

ARVO Annual Meeting Abstract May 2004

Dominant Optic Atrophy, Sensorineural Hearing Loss, Ptosis, and Ophthalmoplegia: A Syndrome Caused by a Mutation in OPA1

Z. Yang; M. Payne; C. Weight; E.D. Pearson; Y. Zhao; X. Li; N. Faulkner; B. Katz; J. Warner; K. Zhang

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):1612. doi:

Biochemistry and Molecular Biology September 2001

Locus for Autosomal Recessive Nonsyndromic Persistent Hyperplastic Primary Vitreous

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Shagufta Khaliq; Abdul Hameed; Muhammad Ismail; Khalid Anwar; Bart Leroy; Annette M. Payne; Shomi S. Bhattacharya; S. Qasim Mehdi
TAGS: autosomal recessive inheritance, persistent hyperplastic primary vitreous
Invest. Ophthalmol. Vis. Sci.. 2001; 42(10):2225-2228. doi:

Biochemistry and Molecular Biology June 2001

A New Locus for Autosomal Recessive RP ( RP29 ) Mapping to Chromosome 4q32-q34 in a Pakistani Family

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Abdul Hameed; Shagufta Khaliq; Muhammad Ismail; Khalid Anwar; S. Qasim Mehdi; David Bessant; Annette M. Payne; Shomi S. Bhattacharya
TAGS: autosomal recessive inheritance, chromosomes, family, dna, mutation
Invest. Ophthalmol. Vis. Sci.. 2001; 42(7):1436-1438. doi:

Biochemistry and Molecular Biology November 2000

Novel Locus for Autosomal Recessive Cone–Rod Dystrophy CORD8 Mapping to Chromosome 1q12-Q24

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Shagufta Khaliq; Abdul Hameed; Muhammad Ismail; Khalid Anwar; Bart P. Leroy; S. Qasim Mehdi; Annette M. Payne; Shomi S. Bhattacharya
TAGS: autosomal recessive inheritance, chromosomes, progressive cone-rod dystrophy, retinitis pigmentosa, dna, mutation, family
Invest. Ophthalmol. Vis. Sci.. 2000; 41(12):3709-3712. doi:

Biochemistry and Molecular Biology March 2000

A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13

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Abdul Hameed; Shagufta Khaliq; Muhammed Ismail; Khalid Anwar; Neil D. Ebenezer; Tim Jordan; S. Qasim Mehdi; Annette M. Payne; Shomi S. Bhattacharya
TAGS: chromosomes, keratoconus, leber's amaurosis, mutation, screening, family, genes
Invest. Ophthalmol. Vis. Sci.. 2000; 41(3):629-633. doi:

Articles May 1981

Clinical and electron microscopic observations of the conjunctiva of adult patients with Bitot's spots.

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J P Ganley; C M Payne
TAGS: adult, conjunctiva, exanthema
Invest. Ophthalmol. Vis. Sci.. 1981; 20(5):632-643. doi:

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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Copyright © 2015 Association for Research in Vision and Ophthalmology.

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