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...

Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options

Ophthalmic genetics, 2018-03, Vol.39 (2), p.149-157

2018

Volltextzugriff (PDF)

fMRI and gene therapy in adults with CNGB3 mutation

Brain research bulletin, 2024-09, Vol.215, p.111026, Article 111026

2024

Volltextzugriff (PDF)

Isolated dislocation of a supplementary sulcus pseudophakic intraocular lens

Journal of cataract and refractive surgery, 2015-06, Vol.41 (6), p.1315-1317

2015

Volltextzugriff (PDF)

Retrospective cohort study exploring whether an association exists between spatial distribution of cystoid spaces in cystoid macular oedema secondary to retinitis pigmentosa and response to treatment with carbonic anhydrase inhibitors

British journal of ophthalmology, 2019-02, Vol.103 (2), p.233-237

2019

Volltextzugriff (PDF)

A demonstration of cone function plasticity after gene therapy in achromatopsia

Brain (London, England : 1878), 2022-11, Vol.145 (11), p.3803-3815

2022

Volltextzugriff (PDF)

Deep Phenotyping and Gene Therapy in Patients with Achromatopsia

Hirji, Nashila

2020

Volltextzugriff (PDF)

Nystagmus and optical coherence tomography findings in CNGB3-associated achromatopsia

Journal of AAPOS, 2020-04, Vol.24 (2), p.82.e1-82.e7

2020

Volltextzugriff (PDF)

A demonstration of cone function plasticity after gene therapy in achromatopsia

Journal of vision (Charlottesville, Va.), 2021-09, Vol.21 (9), p.2444

2021

Volltextzugriff (PDF)

Outcomes following implementation of a high-volume medical retina virtual clinic utilising a diagnostic hub during COVID-19

Eye (London), 2022-03, Vol.36 (3), p.627-633

2022

Volltextzugriff (PDF)

Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta

American journal of ophthalmology, 2018-04, Vol.188, p.123-130

2018

Volltextzugriff (PDF)

Intraobserver Repeatability and Interobserver Reproducibility of Foveal Cone Density Measurements in CNGA3- and CNGB3 -Associated Achromatopsia

Translational vision science & technology, 2020-06, Vol.9 (7), p.37-37

2020

Volltextzugriff (PDF)

Management of corneal decompensation 4 decades after Sputnik intraocular lens implantation

Eye & contact lens, 2015-01, Vol.41 (1), p.e1-e4

2015

Volltextzugriff (PDF)

Release of l-aspartate by reversal of glutamate transporters

Neuropharmacology, 2005-11, Vol.49 (6), p.843-849

2005

Volltextzugriff (PDF)

The Causes of Distress in Paediatric Outpatients Receiving Dilating Drops

Open journal of ophthalmology, 2012, Vol.2 (2), p.21-25

2012

Volltextzugriff (PDF)

The Risk of Neuroblastoma in Paediatric Horner Syndrome-A Systematic Reappraisal of the Literature

Neuro-ophthalmology (Amsterdam : Aeolus Press. 1980), 2012-12, Vol.36 (6), p.227-231

2012

Volltextzugriff (PDF)

Internal carotid artery dissection secondary to excessive vocal output

BMJ case reports, 2011-03, Vol.2011 (mar05 1), p.bcr0120113710-bcr0120113710

2011

Volltextzugriff (PDF)

Internal carotid artery dissection secondary to excessive vocal output

BMJ Case Reports, 2011, Vol.2011

2011

Volltextzugriff (PDF)

Central serous chorioretinopathy secondary to childbirth

BMJ Case Reports, 2010, Vol.2010

2010

Volltextzugriff (PDF)

1 – 18 von 18

Suche als RSS-Feed

Aktive Filter

ThemaAdult

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(14)
Mit Volltextzugriff
(13)

Publikationsform

Sprache

Englisch
(18)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options

fMRI and gene therapy in adults with CNGB3 mutation

Isolated dislocation of a supplementary sulcus pseudophakic intraocular lens

Retrospective cohort study exploring whether an association exists between spatial distribution of cystoid spaces in cystoid macular oedema secondary to retinitis pigmentosa and response to treatment with carbonic anhydrase inhibitors

A demonstration of cone function plasticity after gene therapy in achromatopsia

Deep Phenotyping and Gene Therapy in Patients with Achromatopsia

Nystagmus and optical coherence tomography findings in CNGB3-associated achromatopsia

A demonstration of cone function plasticity after gene therapy in achromatopsia

Outcomes following implementation of a high-volume medical retina virtual clinic utilising a diagnostic hub during COVID-19

Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta

Intraobserver Repeatability and Interobserver Reproducibility of Foveal Cone Density Measurements in CNGA3- and CNGB3 -Associated Achromatopsia

Management of corneal decompensation 4 decades after Sputnik intraocular lens implantation

Release of l-aspartate by reversal of glutamate transporters

The Causes of Distress in Paediatric Outpatients Receiving Dilating Drops

The Risk of Neuroblastoma in Paediatric Horner Syndrome-A Systematic Reappraisal of the Literature

Internal carotid artery dissection secondary to excessive vocal output

Internal carotid artery dissection secondary to excessive vocal output

Central serous chorioretinopathy secondary to childbirth

Aktive Filter

Suchergebnisse filtern