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List of works by Julie De Zaeytijd

ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants

scientific article published on 23 January 2019

Added value of infrared, red-free and autofluorescence fundus imaging in pseudoxanthoma elasticum

scientific article published in September 2009

Allergy to ophthalmic solutions

scientific article

An atypical case of neurosarcoidosis presenting with neovascular glaucoma

scientific article published on 18 April 2018

An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients.

scientific article published in January 2015

An update on the ocular phenotype in patients with pseudoxanthoma elasticum

scientific article published on 04 April 2013

Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

scientific article published on 31 October 2018

Bilateral Choroidal Metastases from Endobronchial Carcinoid Treated with Somatostatin Analogues

scientific article

Bilateral non-arteritic ischemic optic neuropathy in a transsexual woman using excessive estrogen dosage

scientific article published on 21 September 2013

CLINICAL CHARACTERISTICS AND NATURAL HISTORY OF RHO-ASSOCIATED RETINITIS PIGMENTOSA: A Long-Term Follow-Up Study

scientific article published on 15 April 2020

Characterization of cardiovascular involvement in pseudoxanthoma elasticum families

scientific article published on 22 August 2013

Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290

scientific article published on 01 September 2018

Cognitive outcomes in Susac syndrome: A 2‐year neuropsychological follow‐up study

scholarly article

Colour Vision in Stargardt Disease

scientific article

Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndrome

scientific article published in June 2014

Contact dermatitis in patients undergoing serial intravitreal injections

scientific article published on 22 October 2015

Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

scientific article published on 01 April 2019

DETAILED CLINICAL PHENOTYPING OF OXALATE MACULOPATHY IN PRIMARY HYPEROXALURIA TYPE 1 AND REVIEW OF THE LITERATURE.

scientific article published on 28 April 2016

Diplopia as presenting sign of Turcot syndrome

scientific article

Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

scientific article published on 17 December 2018

Efficacy of Multiple Dexamethasone Intravitreal Implants for Refractory Retinal Vein Occlusion-Related Macular Edema and Effect of Prior Vitrectomy

scientific article published on 07 November 2018

High-resolution optical coherence tomography, autofluorescence, and infrared reflectance imaging in Sjögren reticular dystrophy

scientific article

Long-Read Sequencing to Unravel Complex Structural Variants of <i>CEP78</i> Leading to Cone-Rod Dystrophy and Hearing Loss

scientific article published on 21 April 2021

Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families

scientific article

New variants and in silico analyses in GRK1 associated Oguchi disease

scientific article published on 30 November 2020

Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus.

scientific article published on 12 February 2015

PATHOGENIC VARIANTS IN THE ABCC6 GENE ARE ASSOCIATED WITH AN INCREASED RISK FOR ISCHEMIC STROKE.

scientific article published on 3 May 2018

Peripheral ischaemic retinopathy and neovascularisation in a patient with subacute streptococcus mitis-induced bacterial endocarditis

scientific article published on 12 September 2017

The N-terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond

scientific article published on 06 February 2019

The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR Gene

article

The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56

scientific article published on 28 January 2020

Thrombomodulin and Endothelial Dysfunction: A Disease-Modifier Shared between Malignant Hypertension and Atypical Hemolytic Uremic Syndrome

scientific article published on 25 June 2018

Uveitis and immune checkpoint inhibition: when a blockage isn’t just a blockage ⬇️

scholarly article

VEGFA variants as prognostic markers for the retinopathy in Pseudoxanthoma elasticum

scientific article published on 08 April 2020

Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa

scientific article

Vitreous Hemorrhage as Presenting Sign of Retinal Arteriovenous Malformation

scientific article published on 19 October 2020

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