UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 116

Sortiert nach

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness

American journal of human genetics, 2006-10, Vol.79 (4), p.657-667

2006

Volltextzugriff (PDF)

Long-term prognosis of patients with idiopathic Horner syndrome

Journal of neurology, 2022-05, Vol.269 (5), p.2781-2783

2022

Volltextzugriff (PDF)

Painful Recurrent Diplopia Caused by Medial Rectus Cysticercosis

Neurology, 2021-03, Vol.96 (9), p.452

2021

Volltextzugriff (PDF)

Case Report: Multimodal Imaging of Toxic Retinopathies Related to Human Immunodeficiency Virus Antiretroviral Therapies: Maculopathy vs. Peripheral Retinopathy. Report of Two Cases and Review of the Literature

Frontiers in neurology, 2021-06, Vol.12

2021

Volltextzugriff (PDF)

Clinical impact and misdiagnosis of functional ophthalmological symptoms: a case report

Journal of medical case reports, 2023-08, Vol.17 (1), p.340-340, Article 340

2023

Volltextzugriff (PDF)

Drug- and Toxin-Induced Opsoclonus - a Systematized Review, including a Case Report on Amantadine-Induced Opsoclonus in Multiple System Atrophy

Tremor and other hyperkinetic movements (New York, N.Y.), 2024, Vol.14 (1), p.23-23

2024

Volltextzugriff (PDF)

Cross-sectional study assessing the addition of contrast sensitivity to visual acuity when testing for fitness to drive

BMJ open, 2018-01, Vol.8 (1), p.e018546-e018546

2018

Volltextzugriff (PDF)

The Spectrum of Maculopathy in Mitochondrial DNA A3243G Mutation: A Case Series of Six Patients

Klinische Monatsblatter fur Augenheilkunde, 2021-04, Vol.238 (4), p.414

2021

Volltextzugriff (PDF)

Oculopalatal tremor: current concepts and new observations

Current opinion in neurology, 2013-02, Vol.26 (1), p.67-73

2013

Volltextzugriff (PDF)

In vivo identification of morphologic retinal abnormalities in neuromyelitis optica

Neurology, 2014-01, Vol.82 (2), p.188

Borruat, Francois-Xavier

2014

Volltextzugriff (PDF)

Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature

BMC ophthalmology, 2014-06, Vol.14 (1), p.77-77, Article 77

2014

Volltextzugriff (PDF)

Posterior Cortical Atrophy: Review of the Recent Literature

Current neurology and neuroscience reports, 2013-12, Vol.13 (12), p.406-406, Article 406

Borruat, François-Xavier

2013

Volltextzugriff (PDF)

Acetazolamide Reduces Retinal Inner Nuclear Layer Thickness in Microcystic Macular Edema Secondary to Optic Neuropathy

European neurology, 2018-01, Vol.79 (3-4), p.150-153

2018

Volltextzugriff (PDF)

Homonymous Ganglion Cell Layer Thinning After Isolated Occipital Lesion: Macular OCT Demonstrates Transsynaptic Retrograde Retinal Degeneration

Journal of neuro-ophthalmology, 2015-06, Vol.35 (2), p.112-116

2015

Volltextzugriff (PDF)

Normal Visual Recovery after Optic Neuritis Despite Significant Loss of Retinal Ganglion Cells in Patients with Multiple Sclerosis

Klinische Monatsblatter fur Augenheilkunde, 2019-04, Vol.236 (4), p.425

2019

Volltextzugriff (PDF)

Transient ocular tilt reaction and Tullio phenomenon: A rare association

Neurology, 2015-06, Vol.84 (22), p.2291

2015

Volltextzugriff (PDF)

Tocilizumab for giant cell arteritis with corticosteroid-resistant progressive anterior ischemic optic neuropathy

Joint, bone, spine : revue du rhumatisme, 2017-10, Vol.84 (5), p.615-619

2017

Volltextzugriff (PDF)

Visual signs and symptoms in patients with the visual variant of Alzheimer disease

BMC ophthalmology, 2015-06, Vol.15 (1), p.65-65, Article 65

2015

Volltextzugriff (PDF)

Inner Retinal Dysfunction in the Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Frontiers in neurology, 2017-10, Vol.8, p.523

2017

Volltextzugriff (PDF)

Ocular and Cerebral Emboli From an Atrial Myxoma

Journal of neuro-ophthalmology, 2017-09, Vol.37 (3), p.309-310

2017

Volltextzugriff (PDF)

Novel maculopathy in patients with spinocerebellar ataxia type 1 autofluorescence findings and functional characteristics

JAMA ophthalmology, 2013-04, Vol.131 (4), p.536

2013

Volltextzugriff (PDF)

Residual perception of biological motion in cortical blindness

Neuropsychologia, 2016-12, Vol.93 (Pt A), p.301-311

2016

Volltextzugriff (PDF)

Oculopalatal Tremor: Variations on a Theme by Guillain and Mollaret

European neurology, 2014-01, Vol.72 (3-4), p.144-149

2014

Volltextzugriff (PDF)

Optic neuropathy in patients using amiodarone

Archives of ophthalmology (1960), 2006-05, Vol.124 (5), p.696

2006

Volltextzugriff (PDF)

Differential effect of long versus short wavelength light exposure on pupillary re-dilation in patients with outer retinal disease

Clinical & experimental ophthalmology, 2012-01, Vol.40 (1), p.e16-e24

2012

Volltextzugriff (PDF)

1 – 25 von 116

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(85)
Mit Volltextzugriff
(80)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness

Long-term prognosis of patients with idiopathic Horner syndrome

Painful Recurrent Diplopia Caused by Medial Rectus Cysticercosis

Case Report: Multimodal Imaging of Toxic Retinopathies Related to Human Immunodeficiency Virus Antiretroviral Therapies: Maculopathy vs. Peripheral Retinopathy. Report of Two Cases and Review of the Literature

Clinical impact and misdiagnosis of functional ophthalmological symptoms: a case report

Drug- and Toxin-Induced Opsoclonus - a Systematized Review, including a Case Report on Amantadine-Induced Opsoclonus in Multiple System Atrophy

Cross-sectional study assessing the addition of contrast sensitivity to visual acuity when testing for fitness to drive

The Spectrum of Maculopathy in Mitochondrial DNA A3243G Mutation: A Case Series of Six Patients

Oculopalatal tremor: current concepts and new observations

In vivo identification of morphologic retinal abnormalities in neuromyelitis optica

Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature

Posterior Cortical Atrophy: Review of the Recent Literature

Acetazolamide Reduces Retinal Inner Nuclear Layer Thickness in Microcystic Macular Edema Secondary to Optic Neuropathy

Homonymous Ganglion Cell Layer Thinning After Isolated Occipital Lesion: Macular OCT Demonstrates Transsynaptic Retrograde Retinal Degeneration

Normal Visual Recovery after Optic Neuritis Despite Significant Loss of Retinal Ganglion Cells in Patients with Multiple Sclerosis

Transient ocular tilt reaction and Tullio phenomenon: A rare association

Tocilizumab for giant cell arteritis with corticosteroid-resistant progressive anterior ischemic optic neuropathy

Visual signs and symptoms in patients with the visual variant of Alzheimer disease

Inner Retinal Dysfunction in the Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Ocular and Cerebral Emboli From an Atrial Myxoma

Novel maculopathy in patients with spinocerebellar ataxia type 1 autofluorescence findings and functional characteristics

Residual perception of biological motion in cortical blindness

Oculopalatal Tremor: Variations on a Theme by Guillain and Mollaret

Optic neuropathy in patients using amiodarone

Differential effect of long versus short wavelength light exposure on pupillary re-dilation in patients with outer retinal disease

Suchergebnisse filtern