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Early-Onset Severe Rod-Cone Dystrophy in Young Children with RPE65 Mutations

Investigative ophthalmology & visual science, 2000-08, Vol.41 (9), p.2735-2742

2000

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Correlation of central visual function and ROP risk factors in prematures with and without acute ROP at the age of 6-13years: the Giessen long-term ROP study

British journal of ophthalmology, 2016-09, Vol.100 (9), p.1238-1244

2016

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Correlation of central visual function and ROP risk factors in prematures with and without acute ROP at the age of 6–13 years: the Giessen long-term ROP study

British journal of ophthalmology, 2016-09, Vol.100 (9), p.1238-1244

2016

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Handheld Optical Coherence Tomography in Paediatric Ophthalmology: Experience of the Department of Ophthalmology in Giessen

Klinische Monatsblatter fur Augenheilkunde, 2016-10, Vol.233 (10), p.1142

2016

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Autosomal recessive bestrophinopathy (ARB): a clinical and molecular description of two patients at childhood

Klinische Monatsblatter fur Augenheilkunde, 2012-10, Vol.229 (10), p.1009

2012

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First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis

Journal of medical genetics, 1999-12, Vol.36 (12), p.932-934

1999

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A comparison of two multifocal ERG systems

Documenta ophthalmologica, 1998, Vol.97 (2), p.157-178

1998

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Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration

European journal of human genetics : EJHG, 2000-04, Vol.8 (4), p.286-292

2000

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Phenotype in two families with RP3 associated with RPGR mutations

Ophthalmic genetics, 2003-06, Vol.24 (2), p.89-101

2003

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Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype-phenotype correlation

Graefe's archive for clinical and experimental ophthalmology, 2002-08, Vol.240 (8), p.628-638

2002

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Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis

Clinical genetics, 1999-06, Vol.55 (6), p.461-465

1999

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Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus

Klinische Monatsblätter für Augenheilkunde, 1996-01, Vol.208 (1), p.48

1996

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RETINAL VASCULAR DEVELOPMENT WITH 0.312 MG INTRAVITREAL BEVACIZUMAB TO TREAT SEVERE POSTERIOR RETINOPATHY OF PREMATURITY: A Longitudinal Fluorescein Angiographic Study

Retina (Philadelphia, Pa.), 2017-01, Vol.37 (1), p.97

2017

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Blockchain and Sustainability: A Possible Union?

Technology, Business and Sustainable Development, 2023, Vol.1, p.33-51

1, 2023

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Early-Onset Severe Rod-Cone Dystrophy in Young Children with RPE65 Mutations

Correlation of central visual function and ROP risk factors in prematures with and without acute ROP at the age of 6-13years: the Giessen long-term ROP study

Correlation of central visual function and ROP risk factors in prematures with and without acute ROP at the age of 6–13 years: the Giessen long-term ROP study

Handheld Optical Coherence Tomography in Paediatric Ophthalmology: Experience of the Department of Ophthalmology in Giessen

Autosomal recessive bestrophinopathy (ARB): a clinical and molecular description of two patients at childhood

First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis

A comparison of two multifocal ERG systems

Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration

Phenotype in two families with RP3 associated with RPGR mutations

Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype-phenotype correlation

Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis

Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus

RETINAL VASCULAR DEVELOPMENT WITH 0.312 MG INTRAVITREAL BEVACIZUMAB TO TREAT SEVERE POSTERIOR RETINOPATHY OF PREMATURITY: A Longitudinal Fluorescein Angiographic Study

Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response

Blockchain and Sustainability: A Possible Union?

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