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

British journal of ophthalmology, 2014-02, Vol.98 (2), p.159-161

2014

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The Role of Inflammation in the Pathogenesis of Age-related Macular Degeneration

Survey of ophthalmology, 2006-03, Vol.51 (2), p.137-152

2006

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The Role of Complement Factor H in Age-related Macular Degeneration: A Review

Survey of ophthalmology, 2010-05, Vol.55 (3), p.227-246

2010

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Role of complement cascade in abdominal aortic aneurysms

Arteriosclerosis, thrombosis, and vascular biology, 2011-07, Vol.31 (7), p.1653-1660

2011

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Neuroprotection for glaucoma: Requirements for clinical translation

Experimental eye research, 2017-04, Vol.157, p.34-37

2017

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X-linked retinoschisis: A clinical and molecular genetic review

Survey of ophthalmology, 2004-03, Vol.49 (2), p.214-230

2004

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Analysis of Six Genetic Risk Factors Highly Associated with AMD in the Region Surrounding ARMS2 and HTRA1 on Chromosome 10, Region q26

Investigative ophthalmology & visual science, 2010-04, Vol.51 (4), p.2191-2196

2010

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Repertoire Analysis and New Pathogenic Epitopes of IRBP in C57BL/6 (H-2b) and B10.RIII (H-2r) Mice

Investigative ophthalmology & visual science, 2008-05, Vol.49 (5), p.1946-1956

2008

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False eyes: eyes to show and eyes to see

British journal of ophthalmology, 2011-04, Vol.95 (4), p.476-476

2011

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An immunologically privileged retinal antigen elicits tolerance: major role for central selection mechanisms

The Journal of experimental medicine, 2003-12, Vol.198 (11), p.1665-1676

2003

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Clinical Variability of Stickler Syndrome: Role of Exon 2 of the Collagen COL2A1 Gene

Survey of ophthalmology, 2003-03, Vol.48 (2), p.191-203

2003

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A humanized model of experimental autoimmune uveitis in HLA class II transgenic mice

The Journal of clinical investigation, 2003-04, Vol.111 (8), p.1171-1180

2003

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Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome family

American journal of ophthalmology, 2002-11, Vol.134 (5), p.720-727

2002

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Autosomal Dominant Stargardt-Like Macular Dystrophy

Survey of ophthalmology, 2001-09, Vol.46 (2), p.149-163

2001

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Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14

American journal of ophthalmology, 1999-04, Vol.127 (4), p.426-435

1999

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

Retina (Philadelphia, Pa.), 2006-10, Vol.26 (8), p.940-946

2006

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The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity

Nature (London), 1987-10, Vol.329 (6140), p.642-645

1987

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

Retina (Philadelphia, Pa.), 2005-12, Vol.25 (8), p.999-1004

2005

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

American journal of ophthalmology, 2003-09, Vol.136 (3), p.542-545

2003

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Interphotoreceptor retinoid-binding protein (IRBP)-deficient C57BL/6 mice have enhanced immunological and immunopathogenic responses to IRBP and an altered recognition of IRBP epitopes

Journal of autoimmunity, 2003-11, Vol.21 (3), p.185-194

2003

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Malattia leventinese presenting with subretinal neovascular membrane and hemorrhage

American journal of ophthalmology, 2001-04, Vol.131 (4), p.517-518

2001

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X-linked retinoschisis: report of a family with a rare deletion in the xLRS1 gene

American journal of ophthalmology, 2003-09, Vol.136 (3), p.547-549

2003

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Author's Response

Survey of ophthalmology, 2006-09, Vol.51 (5), p.532

Donoso, Larry A.

2006

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A Novel Gene for Autosomal Dominant Stargardt-like Macular Dystrophy with Homology to the SUR4 Protein Family

Investigative ophthalmology & visual science, 2001-10, Vol.42 (11), p.2652-2663

2001

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Autosomal dominant macular dystrophy in a large Canadian family

Canadian journal of ophthalmology, 2003-02, Vol.38 (1), p.33-40

2003

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

The Role of Inflammation in the Pathogenesis of Age-related Macular Degeneration

The Role of Complement Factor H in Age-related Macular Degeneration: A Review

Role of complement cascade in abdominal aortic aneurysms

Neuroprotection for glaucoma: Requirements for clinical translation

X-linked retinoschisis: A clinical and molecular genetic review

Analysis of Six Genetic Risk Factors Highly Associated with AMD in the Region Surrounding ARMS2 and HTRA1 on Chromosome 10, Region q26

Repertoire Analysis and New Pathogenic Epitopes of IRBP in C57BL/6 (H-2b) and B10.RIII (H-2r) Mice

False eyes: eyes to show and eyes to see

An immunologically privileged retinal antigen elicits tolerance: major role for central selection mechanisms

Clinical Variability of Stickler Syndrome: Role of Exon 2 of the Collagen COL2A1 Gene

A humanized model of experimental autoimmune uveitis in HLA class II transgenic mice

Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome family

Autosomal Dominant Stargardt-Like Macular Dystrophy

Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14

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

The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity

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

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

Interphotoreceptor retinoid-binding protein (IRBP)-deficient C57BL/6 mice have enhanced immunological and immunopathogenic responses to IRBP and an altered recognition of IRBP epitopes

Malattia leventinese presenting with subretinal neovascular membrane and hemorrhage

X-linked retinoschisis: report of a family with a rare deletion in the xLRS1 gene

Author's Response

A Novel Gene for Autosomal Dominant Stargardt-like Macular Dystrophy with Homology to the SUR4 Protein Family

Autosomal dominant macular dystrophy in a large Canadian family

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