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The Association between Visual Acuity and Central Retinal Thickness in Retinitis Pigmentosa

Investigative ophthalmology & visual science, 2005-09, Vol.46 (9), p.3349-3354

2005

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'Everything Changes in Nature': Kropotkin's Process Philosophy

Anarchist Studies, 2023-09, Vol.31 (2), p.16-33

Sandberg, Ole Martin

2023

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Night Blindness and Abnormal Cone Electroretinogram ON Responses in Patients with Mutations in the GRM6 Gene Encoding mGluR6

Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (13), p.4884-4889

2005

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Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis

Human gene therapy, 2010-08, Vol.21 (8), p.993-1004

2010

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RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa

American journal of human genetics, 2003-11, Vol.73 (5), p.1131-1146

2003

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Cone cGMP‐gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases

Human mutation, 2005-03, Vol.25 (3), p.248-258

2005

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A Retinitis Pigmentosa GTPase Regulator (RPGR)-Deficient Mouse Model for X-Linked Retinitis Pigmentosa (RP3)

Proceedings of the National Academy of Sciences - PNAS, 2000-03, Vol.97 (7), p.3649-3654

2000

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Disease Progression in Patients with Dominant Retinitis Pigmentosa and Rhodopsin Mutations

Investigative ophthalmology & visual science, 2002-09, Vol.43 (9), p.3027-3036

2002

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Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP

Investigative ophthalmology & visual science, 2005-09, Vol.46 (9), p.3039-3045

2005

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AIPL1, the Protein That Is Defective in Leber Congenital Amaurosis, Is Essential for the Biosynthesis of Retinal Rod cGMP Phosphodiesterase

Proceedings of the National Academy of Sciences - PNAS, 2004-09, Vol.101 (38), p.13903-13908

2004

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Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation

Nature, 2004-01, Vol.427 (6969), p.75-78

2004

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Recessive NRL Mutations in Patients with Clumped Pigmentary Retinal Degeneration and Relative Preservation of Blue Cone Function

Proceedings of the National Academy of Sciences - PNAS, 2004-12, Vol.101 (51), p.17819-17824

2004

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A Single, Abbreviated RPGR-ORF15 Variant Reconstitutes RPGR Function In Vivo

Investigative ophthalmology & visual science, 2005-02, Vol.46 (2), p.435-441

2005

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Effect of Vitamin A Supplementation on Rhodopsin Mutants threonine-17→ methionine and proline-347→ serine in Transgenic Mice and in Cell Cultures

Proceedings of the National Academy of Sciences - PNAS, 1998-09, Vol.95 (20), p.11933-11938

1998

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Recessive mutations in the gene encoding the β-subunit of rod phosphodiesterase in patients with retinitis pigmentosa

Nature genetics, 1993-06, Vol.4 (2), p.130-134

1993

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Natural Course of Ocular Function in Pigmented Paravenous Retinochoroidal Atrophy

American journal of ophthalmology, 2006-04, Vol.141 (4), p.763-765

2006

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X-Linked Retinitis Pigmentosa: Mutation Spectrum of the RPGR and RP2 Genes and Correlation with Visual Function

Investigative ophthalmology & visual science, 2000-08, Vol.41 (9), p.2712-2721

2000

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Screen of the IMPDH1 Gene among Patients with Dominant Retinitis Pigmentosa and Clinical Features Associated with the Most Common Mutation, Asp226Asn

Investigative ophthalmology & visual science, 2005-05, Vol.46 (5), p.1735-1741

2005

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Disease Course of Patients With Pericentral Retinitis Pigmentosa

American journal of ophthalmology, 2005-07, Vol.140 (1), p.100.e1-100.e8

2005

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Reading speed of patients with advanced retinitis pigmentosa or choroideremia

Retina (Philadelphia, Pa.), 2006-01, Vol.26 (1), p.80-88

2006

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Clinical Features and Mutations in Patients with Dominant Retinitis Pigmentosa-1 (RP1)

Investigative ophthalmology & visual science, 2001-09, Vol.42 (10), p.2217-2224

2001

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Absence of Photoreceptor Rescue with D-cis-Diltiazem in the rd Mouse

Investigative ophthalmology & visual science, 2002-06, Vol.43 (6), p.1912-1915

2002

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A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

Nature (London), 1990-01, Vol.343 (6256), p.364-366

1990

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A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

Nature genetics, 1992-06, Vol.1 (3), p.209-213

1992

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Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa

The New England journal of medicine, 1990-11, Vol.323 (19), p.1302-1307

1990

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The Association between Visual Acuity and Central Retinal Thickness in Retinitis Pigmentosa

'Everything Changes in Nature': Kropotkin's Process Philosophy

Night Blindness and Abnormal Cone Electroretinogram ON Responses in Patients with Mutations in the GRM6 Gene Encoding mGluR6

Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis

RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa

Cone cGMP‐gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases

A Retinitis Pigmentosa GTPase Regulator (RPGR)-Deficient Mouse Model for X-Linked Retinitis Pigmentosa (RP3)

Disease Progression in Patients with Dominant Retinitis Pigmentosa and Rhodopsin Mutations

Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP

AIPL1, the Protein That Is Defective in Leber Congenital Amaurosis, Is Essential for the Biosynthesis of Retinal Rod cGMP Phosphodiesterase

Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation

Recessive NRL Mutations in Patients with Clumped Pigmentary Retinal Degeneration and Relative Preservation of Blue Cone Function

A Single, Abbreviated RPGR-ORF15 Variant Reconstitutes RPGR Function In Vivo

Effect of Vitamin A Supplementation on Rhodopsin Mutants threonine-17→ methionine and proline-347→ serine in Transgenic Mice and in Cell Cultures

Recessive mutations in the gene encoding the β-subunit of rod phosphodiesterase in patients with retinitis pigmentosa

Natural Course of Ocular Function in Pigmented Paravenous Retinochoroidal Atrophy

X-Linked Retinitis Pigmentosa: Mutation Spectrum of the RPGR and RP2 Genes and Correlation with Visual Function

Screen of the IMPDH1 Gene among Patients with Dominant Retinitis Pigmentosa and Clinical Features Associated with the Most Common Mutation, Asp226Asn

Disease Course of Patients With Pericentral Retinitis Pigmentosa

Reading speed of patients with advanced retinitis pigmentosa or choroideremia

Clinical Features and Mutations in Patients with Dominant Retinitis Pigmentosa-1 (RP1)

Absence of Photoreceptor Rescue with D-cis-Diltiazem in the rd Mouse

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa

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