UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

A cross-linked hyaluronic acid hydrogel (Healaflow®) as a novel vitreous substitute

Graefe's archive for clinical and experimental ophthalmology, 2016-04, Vol.254 (4), p.697-703

2016

Volltextzugriff (PDF)

homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene

Proceedings of the National Academy of Sciences - PNAS, 2009-11, Vol.106 (46), p.19581-19586

2009

Volltextzugriff (PDF)

A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing

Genes, 2023-07, Vol.14 (7), p.1413

2023

Volltextzugriff (PDF)

Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?

Parkinsonism & related disorders, 2020-10, Vol.79, p.138-140

2020

Volltextzugriff (PDF)

Cone implicit time as a predictor of visual outcome in macular hole surgery

Graefe's archive for clinical and experimental ophthalmology, 2014-12, Vol.252 (12), p.1903-1909

2014

Volltextzugriff (PDF)

Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene

Ophthalmic genetics, 2021-04, Vol.42 (2), p.161-169

2021

Volltextzugriff (PDF)

Full-Field Electroretinography Changes Associated with Age-Related Macular Degeneration: A Systematic Review with Meta-Analyses

Ophthalmologica (Basel), 2022-06, Vol.245 (3), p.195-203

2022

Volltextzugriff (PDF)

The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial

Investigative ophthalmology & visual science, 2017-02, Vol.58 (2), p.821-832

2017

Volltextzugriff (PDF)

Attenuation of the retinal nerve fibre layer and reduced retinal function assessed by optical coherence tomography and full‐field electroretinography in patients exposed to vigabatrin medication

Acta ophthalmologica (Oxford, England), 2014-03, Vol.92 (2), p.149-157

2014

Volltextzugriff (PDF)

Macular function measured by binocular mfERG and compared with macular structure in healthy children

Documenta ophthalmologica, 2015-12, Vol.131 (3), p.169-176

2015

Volltextzugriff (PDF)

Full‐field electroretinography in age‐related macular degeneration: an overall retinal response

Acta ophthalmologica (Oxford, England), 2021-03, Vol.99 (2), p.e253-e259

2021

Volltextzugriff (PDF)

Retinal Function and Morphology in the Rabbit Eye after Intravitreal Injection of the TNF Alpha Inhibitor Adalimumab

Current eye research, 2014-11, Vol.39 (11), p.1106-1116

2014

Volltextzugriff (PDF)

A novel phenotype associated with the R162W variant in the KCNJ13 gene

Ophthalmic genetics, 2022-07, Vol.43 (4), p.1-507

2022

Volltextzugriff (PDF)

Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC

Neurobiology of disease, 2017-02, Vol.98, p.36-51

2017

Volltextzugriff (PDF)

Full‐field Electroretinography in Age‐related Macular Degeneration: can retinal electrophysiology predict the subjective visual outcome of cataract surgery?

Acta ophthalmologica (Oxford, England), 2020-11, Vol.98 (7), p.693-700

2020

Volltextzugriff (PDF)

Alteration of vitreal retinoschisin level in human primary retinal detachment

JAMA ophthalmology, 2014-03, Vol.132 (3), p.353

2014

Volltextzugriff (PDF)

Vitreous levels of oxidative stress biomarkers and the radical-scavenger α1-microglobulin/A1M in human rhegmatogenous retinal detachment

Graefe's archive for clinical and experimental ophthalmology, 2013-03, Vol.251 (3), p.725-732

2013

Volltextzugriff (PDF)

Experimental vitreous tamponade using polyalkylimide hydrogel

Graefe's archive for clinical and experimental ophthalmology, 2011-08, Vol.249 (8), p.1167-1174

2011

Volltextzugriff (PDF)

Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?

Parkinsonism & related disorders, 2019-04, Vol.61, p.245-247

2019

Volltextzugriff (PDF)

A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa

Ophthalmic genetics, 2019-03, Vol.40 (2), p.177-181

2019

Volltextzugriff (PDF)

Genotype and Phenotype in an unusual form of Laurence–Moon–Bardet–Biedl syndrome

Acta ophthalmologica (Oxford, England), 2017-05, Vol.95 (3), p.e250-e252

2017

Volltextzugriff (PDF)

Aryl Hydrocarbon Receptor-Interacting Protein-Like 1 in Cancer-Associated Retinopathy

Ophthalmology (Rochester, Minn.), 2016-06, Vol.123 (6), p.1401-1404

2016

Volltextzugriff (PDF)

Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1

Investigative ophthalmology & visual science, 2010-09, Vol.51 (9), p.4754-4765

2010

Volltextzugriff (PDF)

Evaluation of viscoelastic poly(ethylene glycol) sols as vitreous substitutes in an experimental vitrectomy model in rabbits

Acta biomaterialia, 2011-03, Vol.7 (3), p.936-943

2011

Volltextzugriff (PDF)

1 – 25 von 184

Suche als RSS-Feed

Aktive Filter

ThemaMutation

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(149)
Mit Volltextzugriff
(139)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A cross-linked hyaluronic acid hydrogel (Healaflow®) as a novel vitreous substitute

homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene

A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing

Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?

Cone implicit time as a predictor of visual outcome in macular hole surgery

Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene

Full-Field Electroretinography Changes Associated with Age-Related Macular Degeneration: A Systematic Review with Meta-Analyses

The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial

Attenuation of the retinal nerve fibre layer and reduced retinal function assessed by optical coherence tomography and full‐field electroretinography in patients exposed to vigabatrin medication

Macular function measured by binocular mfERG and compared with macular structure in healthy children

Full‐field electroretinography in age‐related macular degeneration: an overall retinal response

Retinal Function and Morphology in the Rabbit Eye after Intravitreal Injection of the TNF Alpha Inhibitor Adalimumab

A novel phenotype associated with the R162W variant in the KCNJ13 gene

Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC

Full‐field Electroretinography in Age‐related Macular Degeneration: can retinal electrophysiology predict the subjective visual outcome of cataract surgery?

Alteration of vitreal retinoschisin level in human primary retinal detachment

Vitreous levels of oxidative stress biomarkers and the radical-scavenger α1-microglobulin/A1M in human rhegmatogenous retinal detachment

Experimental vitreous tamponade using polyalkylimide hydrogel

Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?

A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa

Genotype and Phenotype in an unusual form of Laurence–Moon–Bardet–Biedl syndrome

Aryl Hydrocarbon Receptor-Interacting Protein-Like 1 in Cancer-Associated Retinopathy

Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1

Evaluation of viscoelastic poly(ethylene glycol) sols as vitreous substitutes in an experimental vitrectomy model in rabbits

Clinical Phenotype and Course of PDE6A -Associated Retinitis Pigmentosa Disease, Characterized in Preparation for a Gene Supplementation Trial

Aktive Filter

Suchergebnisse filtern