UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 48

Sortiert nach

Genetic findings of inherited retinal diseases in France

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279)

2024

Link zum Volltext

Verfügbarkeit prüfen

The importance of precisely phenotyping patients with high myopia

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279)

2024

Link zum Volltext

Verfügbarkeit prüfen

Martinique Crinkled Retinal Pigment Epitheliopathy

Ophthalmology (Rochester, Minn.), 2016-10, Vol.123 (10), p.2196-2204

2016

Link zum Volltext

Verfügbarkeit prüfen

Retinitis Punctata Albescens and RLBP1-Allied Phenotypes

Ophthalmology science (Online), 2021-09, Vol.1 (3), p.100052, Article 100052

2021

Link zum Volltext

Verfügbarkeit prüfen

Retinal gene therapy clinical trials are addressing disease at core: Studies are uncovering a range of potential treatments for genetic disorders

Ophthalmology times Europe, 2021-06, Vol.17 (5), p.28

2021

Link zum Volltext

Verfügbarkeit prüfen

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)

2024

Link zum Volltext

Verfügbarkeit prüfen

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)

2024

Link zum Volltext

Verfügbarkeit prüfen

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)

2024

Link zum Volltext

Verfügbarkeit prüfen

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)

2024

Link zum Volltext

Verfügbarkeit prüfen

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)

2024

Link zum Volltext

Verfügbarkeit prüfen

Extensive Macular Atrophy with Pseudodrusen-like appearance (EMAP): progression kinetics and late-stage findings

Ophthalmology (Rochester, Minn.), 2024-04

2024

Link zum Volltext

Verfügbarkeit prüfen

Didanosine-induced retinopathy: new insights with long-term follow-up Authors

Ocular immunology and inflammation, 2021-07, p.1-8

2021

Link zum Volltext

Verfügbarkeit prüfen

Functional Vision in Patients with Bi-allelic USH2A Variants

American journal of ophthalmology, 2023-12

2023

Link zum Volltext

Verfügbarkeit prüfen

Do differentially expressed genes explain high myopia in congenital stationary night blindness?

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279)

2024

Link zum Volltext

Verfügbarkeit prüfen

Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy

Genetics in medicine, 2024-01, p.101081-101081, Article 101081

2024

Link zum Volltext

Verfügbarkeit prüfen

Establishment and measurement of myopia in mice with ON‐bipolar cell defects

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

Link zum Volltext

Verfügbarkeit prüfen

Shedding light on myopia by studying complete congenital stationary night blindness

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

Link zum Volltext

Verfügbarkeit prüfen

QR‐421a RNA therapy in retinitis pigmentosa due to mutations in USH2A: Stellar trial Phase[AP1] 1b/2 interim results

Acta ophthalmologica (Oxford, England), 2022-01, Vol.100 (S267), p.n/a

2022

Link zum Volltext

Verfügbarkeit prüfen

LRIT 3 is essential to localize TRPM 1 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

Link zum Volltext

Verfügbarkeit prüfen

RETINOCHOROIDAL ANASTOMOSIS ASSOCIATED WITH ENHANCED S-CONE SYNDROME

Retinal cases & brief reports, 2019, Vol.13 (4), p.295

2019

Link zum Volltext

Verfügbarkeit prüfen

Lrit3 Deficient Mouse

PloS one, 2014-03, Vol.9 (3), p.e90342

2014

Link zum Volltext

Verfügbarkeit prüfen

Protocole national de diagnostic et de soins (PNDS) de l’aniridie congénitale : synthèse pour le médecin traitant

Journal français d'ophtalmologie, 2022-06, Vol.45 (6), p.647-652

2022

Link zum Volltext

Verfügbarkeit prüfen

Clinical Characteristics and Risk Factors of Extensive Macular Atrophy with Pseudodrusen

Ophthalmology (Rochester, Minn.), 2016-09, Vol.123 (9), p.1865-1873

2016

Link zum Volltext

Verfügbarkeit prüfen

Research Article Cone Dystrophy in Patient with Homozygous RP1L1 Mutation

BioMed research international, 2015

2015

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 48

Suche als RSS-Feed

Aktive Filter

ThemaYoung Adult

ThemaScience & Technology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(30)
Mit Volltextzugriff
(37)

Publikationsform

Sprache

Englisch
(43)
Französisch
(5)

Erscheinungsjahr

n.n

Thema

Ophthalmology
(5)
Humans
(4)
Life Sciences
(4)
Mutation
(4)
Clinical Trials
(3)
Gene Therapy
(3)
Human Health And Pathology
(3)
Retina
(3)
Animal Models
(2)
Animals
(2)
Bipolar Cells
(2)
Congenital Stationary Night Blindness
(2)
Csnb
(2)
Disease Models, Animal
(2)
Environmental Factors
(2)
Eye
(2)
Genes
(2)
Handicap Visuel
(2)
Male
(2)
Mice
(2)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Genetic findings of inherited retinal diseases in France

The importance of precisely phenotyping patients with high myopia

Martinique Crinkled Retinal Pigment Epitheliopathy

Retinitis Punctata Albescens and RLBP1-Allied Phenotypes

Retinal gene therapy clinical trials are addressing disease at core: Studies are uncovering a range of potential treatments for genetic disorders

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

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

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

Extensive Macular Atrophy with Pseudodrusen-like appearance (EMAP): progression kinetics and late-stage findings

Didanosine-induced retinopathy: new insights with long-term follow-up Authors

Functional Vision in Patients with Bi-allelic USH2A Variants

Do differentially expressed genes explain high myopia in congenital stationary night blindness?

Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy

Establishment and measurement of myopia in mice with ON‐bipolar cell defects

Shedding light on myopia by studying complete congenital stationary night blindness

QR‐421a RNA therapy in retinitis pigmentosa due to mutations in USH2A: Stellar trial Phase[AP1] 1b/2 interim results

LRIT 3 is essential to localize TRPM 1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation

RETINOCHOROIDAL ANASTOMOSIS ASSOCIATED WITH ENHANCED S-CONE SYNDROME

The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family

Lrit3 Deficient Mouse

Protocole national de diagnostic et de soins (PNDS) de l’aniridie congénitale : synthèse pour le médecin traitant

Clinical Characteristics and Risk Factors of Extensive Macular Atrophy with Pseudodrusen

Research Article Cone Dystrophy in Patient with Homozygous RP1L1 Mutation

Aktive Filter

Suchergebnisse filtern