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Orbital floor fracture repair: the endonasal approach

Rhinology, 2017-12, Vol.55 (4), p.348-354

2017

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CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders

American journal of human genetics, 2001-10, Vol.69 (4), p.722-737

2001

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TGF- Signaling Protects Retinal Neurons from Programmed Cell Death during the Development of the Mammalian Eye

The Journal of neuroscience, 2013-08, Vol.33 (35), p.14246-14258

2013

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Is there a pathomechanical explanation for unilateral retinal haemorrhages in non-accidental head injury?

Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft, 2021-01, Vol.118 (1), p.76-76

2021

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The agonistic TSPO ligand XBD173 attenuates the glial response thereby protecting inner retinal neurons in a murine model of retinal ischemia

Journal of neuroinflammation, 2019-02, Vol.16 (1), p.43-43, Article 43

2019

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Cone and cone–rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation

British journal of ophthalmology, 2008-08, Vol.92 (8), p.1086-1091

2008

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A luminous efficiency function, V(lambda), for daylight adaptation

Journal of vision (Charlottesville, Va.), 2005-12, Vol.5 (11), p.948-968

2005

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Netzhautbeteiligung bei Muskeldystrophien

Klinische Monatsblätter für Augenheilkunde, 2016-03, Vol.232 (3), p.251-256

Jägle, H.

2016

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Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21

Human molecular genetics, 2000-09, Vol.9 (14), p.2107-2116

2000

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Cre recombinase expression or topical tamoxifen treatment do not affect retinal structure and function, neuronal vulnerability or glial reactivity in the mouse eye

Neuroscience, 2016-06, Vol.325, p.188-201

2016

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Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

Nature genetics, 1998-07, Vol.19 (3), p.257-259

1998

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Macular pigment densities derived from central and peripheral spectral sensitivity differences

Vision research (Oxford), 1998-11, Vol.38 (21), p.3233-3239

1998

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Red, Green, and Red-Green Hybrid Pigments in the Human Retina: Correlations between Deduced Protein Sequences and Psychophysically Measured Spectral Sensitivities

The Journal of neuroscience, 1998-12, Vol.18 (23), p.10053-10069

1998

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Erratum zu: Unilaterale Netzhautblutungen bei Säuglingen – 2 Fälle von Schütteltrauma?

Die Ophthalmologie, 2022-07, Vol.119 (S2), p.149-149

2022

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Die Ophthalmologie

Die Ophthalmologie, 2022-07, Vol.119, p.149-149

2022

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Reorganization of human cortical maps caused by inherited photoreceptor abnormalities

Nature neuroscience, 2002-04, Vol.5 (4), p.364-370

2002

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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

European journal of human genetics : EJHG, 2005-03, Vol.13 (3), p.302-308

2005

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Color vision and the diagnosis of reduced visual acuity

Klinische Monatsblätter für Augenheilkunde, 2004-09, Vol.221 (9), p.739

Jägle, H

2004

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V ( ): a generalized luminous efficiency function for any condition of chromatic adaptation

Journal of vision (Charlottesville, Va.), 2010-03, Vol.7 (9), p.793-793

2010

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Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa

British journal of ophthalmology, 2005-10, Vol.89 (10), p.1258-1264

2005

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The dependence of luminous efficiency on chromatic adaptation

Journal of vision (Charlottesville, Va.), 2008-12, Vol.8 (16), p.1.1-1

2008

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S.P.62 Ocular characteristics of Duchenne Muscular Dystrophy

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.888-888

2012

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P16 Ocular findings in Duchenne muscular dystrophy – an observational case series

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S11-S11

2012

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Visual short-term effects of viagra: double-blind study in healthy young subjects

American journal of ophthalmology, 2004-05, Vol.137 (5), p.842-849

2004

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Muscular Dystrophies Involving the Retinal Function

Klinische Monatsblatter fur Augenheilkunde, 2016-03, Vol.232 (3), p.251

Jägle, H

2016

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Orbital floor fracture repair: the endonasal approach

CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders

TGF- Signaling Protects Retinal Neurons from Programmed Cell Death during the Development of the Mammalian Eye

Is there a pathomechanical explanation for unilateral retinal haemorrhages in non-accidental head injury?

The agonistic TSPO ligand XBD173 attenuates the glial response thereby protecting inner retinal neurons in a murine model of retinal ischemia

Cone and cone–rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation

A luminous efficiency function, V(lambda), for daylight adaptation

Netzhautbeteiligung bei Muskeldystrophien

Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21

Cre recombinase expression or topical tamoxifen treatment do not affect retinal structure and function, neuronal vulnerability or glial reactivity in the mouse eye

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

Macular pigment densities derived from central and peripheral spectral sensitivity differences

Red, Green, and Red-Green Hybrid Pigments in the Human Retina: Correlations between Deduced Protein Sequences and Psychophysically Measured Spectral Sensitivities

Erratum zu: Unilaterale Netzhautblutungen bei Säuglingen – 2 Fälle von Schütteltrauma?

Die Ophthalmologie

Reorganization of human cortical maps caused by inherited photoreceptor abnormalities

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

Color vision and the diagnosis of reduced visual acuity

V ( ): a generalized luminous efficiency function for any condition of chromatic adaptation

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa

The dependence of luminous efficiency on chromatic adaptation

S.P.62 Ocular characteristics of Duchenne Muscular Dystrophy

P16 Ocular findings in Duchenne muscular dystrophy – an observational case series

Visual short-term effects of viagra: double-blind study in healthy young subjects

Muscular Dystrophies Involving the Retinal Function

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