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...

Congenital stationary night blindness: An analysis and update of genotype–phenotype correlations and pathogenic mechanisms

Progress in retinal and eye research, 2015-03, Vol.45, p.58-110

2015

Volltextzugriff (PDF)

Neoplasia and intraocular inflammation: From masquerade syndromes to immunotherapy-induced uveitis

Progress in retinal and eye research, 2019-09, Vol.72, p.100761-100761, Article 100761

2019

Volltextzugriff (PDF)

Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9)

JAMA ophthalmology, 2017-11, Vol.135 (11), p.1232

2017

Volltextzugriff (PDF)

Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome

Human molecular genetics, 2015-01, Vol.24 (1), p.230-242

2015

Volltextzugriff (PDF)

Delayed-onset hypoxic cortical blindness: coming back from the abyss

Documenta ophthalmologica, 2022-04, Vol.144 (2), p.147-152

2022

Volltextzugriff (PDF)

LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation

The European journal of neuroscience, 2015-08, Vol.42 (3), p.1966-1975

2015

Volltextzugriff (PDF)

Genetic findings of inherited retinal diseases in France

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

2024

Volltextzugriff (PDF)

The importance of precisely phenotyping patients with high myopia

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

2024

Volltextzugriff (PDF)

RP1 and autosomal dominant rod-cone dystrophy: Novel mutations, a review of published variants, and genotype-phenotype correlation

Human mutation, 2012-01, Vol.33 (1), p.73-80

2012

Volltextzugriff (PDF)

Functional and high resolution retinal imaging assessment in a case of ocular siderosis

Documenta ophthalmologica, 2014-02, Vol.128 (1), p.69-75

2014

Volltextzugriff (PDF)

Challenges of Phenotype-Genotype Correlations in Rare Diseases-Reply

JAMA ophthalmology, 2021-12, Vol.139 (12), p.1323

2021

Volltextzugriff (PDF)

Non-vasogenic cystoid maculopathies

Progress in retinal and eye research, 2022-11, Vol.91, p.101092, Article 101092

2022

Volltextzugriff (PDF)

WOMEN in EVER is supporting women researchers, clinicians, and academic staff in their career development with a goal to prepare them for leadership roles in the scientific community

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

2024

Volltextzugriff (PDF)

We would like to especially recognize the creativity, energy, and substantive contributions from all women in ophthalmology and vision science! You have brought a fresh and much needed perspective to EVER

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

2024

Volltextzugriff (PDF)

This WOMEN in EVER session is connecting early‐career and leading women scientists from all over Europe to tackle the underrepresentation of women in science by increasing visibility

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

2024

Volltextzugriff (PDF)

It is our joint task to translate into reality a more equal and connected world for women scientists in all their diversity

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

2024

Volltextzugriff (PDF)

Fostering an international network of women scientists and clinicians, encouraging open dialogue, and inspiring future women scientists in ophthalmology and vision science

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279), p.n/a

2024

Volltextzugriff (PDF)

Adult-onset foveomacular vitelliform dystrophy: A fresh perspective

Progress in retinal and eye research, 2015-07, Vol.47, p.64-85

2015

Volltextzugriff (PDF)

ATXN7-Related Cone-Rod Dystrophy: The Integrated Functional Evaluation of the Cerebellum (CERMOI) Study

JAMA ophthalmology, 2024-04, Vol.142 (4), p.301

2024

Volltextzugriff (PDF)

Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to CLN3 Pathogenic Variants in a French Retinitis Pigmentosa Cohort

JAMA ophthalmology, 2021-03, Vol.139 (3), p.278

2021

Volltextzugriff (PDF)

Association of Missense Variants in VSX2 With a Peculiar Form of Congenital Stationary Night Blindness Affecting All Bipolar Cells

JAMA ophthalmology, 2022-12, Vol.140 (12), p.1163

2022

Volltextzugriff (PDF)

Electrophysiological features and multimodal imaging in ritonavir-related maculopathy

Documenta ophthalmologica, 2017-12, Vol.135 (3), p.241-248

2017

Volltextzugriff (PDF)

MERTK mutation update in inherited retinal diseases

Human mutation, 2018-07, Vol.39 (7), p.887-913

2018

Volltextzugriff (PDF)

Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B

JAMA ophthalmology, 2019-06, Vol.137 (6), p.669

2019

Volltextzugriff (PDF)

1 – 25 von 71

Suche als RSS-Feed

Aktive Filter

KollektionNexis Uni

Zeitschrift / SerieInvestigative Ophthalmology & Visual Science

KollektionOvid SocietyJournals and Single Titles

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(66)
Mit Volltextzugriff
(54)

Publikationsform

Artikel
(70)
Berichte
(1)

Sprache

Englisch
(71)
Japanisch
(9)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Congenital stationary night blindness: An analysis and update of genotype–phenotype correlations and pathogenic mechanisms

Neoplasia and intraocular inflammation: From masquerade syndromes to immunotherapy-induced uveitis

Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9)

Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome

Delayed-onset hypoxic cortical blindness: coming back from the abyss

LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation

Genetic findings of inherited retinal diseases in France

The importance of precisely phenotyping patients with high myopia

RP1 and autosomal dominant rod-cone dystrophy: Novel mutations, a review of published variants, and genotype-phenotype correlation

Functional and high resolution retinal imaging assessment in a case of ocular siderosis

Challenges of Phenotype-Genotype Correlations in Rare Diseases-Reply

Non-vasogenic cystoid maculopathies

WOMEN in EVER is supporting women researchers, clinicians, and academic staff in their career development with a goal to prepare them for leadership roles in the scientific community

We would like to especially recognize the creativity, energy, and substantive contributions from all women in ophthalmology and vision science! You have brought a fresh and much needed perspective to EVER

This WOMEN in EVER session is connecting early‐career and leading women scientists from all over Europe to tackle the underrepresentation of women in science by increasing visibility

It is our joint task to translate into reality a more equal and connected world for women scientists in all their diversity

Fostering an international network of women scientists and clinicians, encouraging open dialogue, and inspiring future women scientists in ophthalmology and vision science

Adult-onset foveomacular vitelliform dystrophy: A fresh perspective

ATXN7-Related Cone-Rod Dystrophy: The Integrated Functional Evaluation of the Cerebellum (CERMOI) Study

Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to CLN3 Pathogenic Variants in a French Retinitis Pigmentosa Cohort

Association of Missense Variants in VSX2 With a Peculiar Form of Congenital Stationary Night Blindness Affecting All Bipolar Cells

Longitudinal Changes of Clinical, Imaging, and Fluid Biomarkers in Preataxic and Early Ataxic Spinocerebellar Ataxia Type 2 and 7 Carriers

Electrophysiological features and multimodal imaging in ritonavir-related maculopathy

MERTK mutation update in inherited retinal diseases

Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B

Aktive Filter

Suchergebnisse filtern