Publications by authors named "Larry A Donoso"

17Publications

Innovations in 3D printing: a 3D overview from optics to organs.

Br J Ophthalmol 2014 Feb 28;98(2):159-61. Epub 2013 Nov 28.

Department of Ophthalmology, Wills Eye Hospital, , Philadelphia, Pennsylvania, USA.

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February 2014

The role of complement Factor H in age-related macular degeneration: a review.

Surv Ophthalmol 2010 May-Jun;55(3):227-46

The Philadelphia Retina Endowment Fund, The Eye Research Institute, Philadelphia, PA, USA.

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May 2010

Repertoire analysis and new pathogenic epitopes of IRBP in C57BL/6 (H-2b) and B10.RIII (H-2r) mice.

Invest Ophthalmol Vis Sci 2008 May;49(5):1946-56

Laboratory of Immunology, National Eye Institute, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA.

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May 2008

X-linked retinoschisis: novel mutation in the initiation codon of the XLRS1 gene in a large family.

Retina 2006 Oct;26(8):940-6

Henry and Corinne Bower Laboratory, Wills Eye Hospital and the Eye Research Institute, 211 South 9th Street, Room 402, Philadelphia, PA 19107, USA.

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October 2006

The role of inflammation in the pathogenesis of age-related macular degeneration.

Surv Ophthalmol 2006 Mar-Apr;51(2):137-52

The Henry and Corinne Bower Laboratory, the Eye Research Institute, Wills Eye Hospital, Philadelphia, Pennsylvania 19105, USA.

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May 2006

Autosomal dominant pattern dystrophy: identification of a novel splice site mutation in the peripherin/RDS gene.

Retina 2005 Dec;25(8):999-1004

Henry and Corinne Bower Laboratory, the Eye Research Institute, the International Retinal Research Foundation, and Wills Eye Hospital, Philadelphia, PA 19107, USA.

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December 2005

X-linked retinoschisis: a clinical and molecular genetic review.

Surv Ophthalmol 2004 Mar-Apr;49(2):214-30

The Henry and Corinne Bower Laboratory, Wills Eye Hospital, and the Eye Research Institute, Philadelphia, Pennsylvania, USA.

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May 2004

X-linked retinoschisis: report of a family with a rare deletion in the XLRS1 gene.

Am J Ophthalmol 2003 Sep;136(3):547-9

Henry and Corinne Bower Laboratory, Wills Eye Hospital and the Eye Research Institute, Philadelphia, Pennsylvania 19107, USA.

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September 2003

Autosomal dominant Stargardt-like macular dystrophy: identification of a new family with a mutation in the ELOVL4 gene.

Am J Ophthalmol 2003 Sep;136(3):542-5

Henry and Corinne Bower Laboratory, the Eye Research Institute and Wills Eye Hospital, Philadelphia, Pennsylvania 19107, USA.

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September 2003

Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 gene.

Surv Ophthalmol 2003 Mar-Apr;48(2):191-203

Henry and Corinne Bower Laboratory, Eye Research Institute, Wills Eye Hospital, 900 Walnut Street, Philadelphia, PA 19107, USA.

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June 2003

Autosomal dominant macular dystrophy in a large Canadian family.

Can J Ophthalmol 2003 Feb;38(1):33-40

Henry and Corinne Bower Laboratory, Eye Research Institute, Wills Eye Hospital, Philadelphia, PA 19107, USA.

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February 2003