Research Explorer

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Researcher

Kristien Hoornaert

Awards & Distinctions

14 Results

2017

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

Laura LeysenElke O. KrepsIlse De SchryverKristien HoornaertVanessa SmithJulie De Zaeytijd

A2 Journal Article in GMS. OPHTHALMOLOGY CASES

2016

Bilateral choroidal metastases from endobronchial carcinoid treated with somatostatin analogues

Deborah De BruynJan LamontErik VanderstraetenSimon Van BelleELISE PLATTEAUJulie De ZaeytijdKristien Hoornaert

A2 Journal Article in OPEN OPHTHALMOLOGY JOURNAL

Do not turn a blind eye to alkyl nitrite (poppers)!

Nathalie OG BralMarina MarinkovicBart LeroyKristien HoornaertMichel van LintMarcel PM ten Tusscher

A1 Journal Article in ACTA OPHTHALMOLOGICA

Stickler syndrome: comprehensive clinical and molecular analysis

Frederic AckePaul CouckeOlivier VanakkerKristien HoornaertGeert MortierIngeborg DhoogeAnne De PaepeEls De LeenheerFransiska Malfait

2015

Prominent Mittendorf spot

Elke O. KrepsPIETER LAMBRECHTBart LeroyKristien Hoornaert

Editorial material

2014

Diagnostic criteria for Stickler syndrome based on comprehensive clinical and molecular analysis

Frederic AckePaul CouckeOlivier VanakkerKristien HoornaertIngeborg DhoogeAnne De PaepeEls De LeenheerFransiska Malfait

2012

Age-dependent ocular phenotype in hereditary hyperferritinaemia cataract syndrome (HHCS)

ELISE PLATTEAUKristien HoornaertKoen MoensBart Leroy

A1 Journal Article in ACTA OPHTHALMOLOGICA

2010

Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients

Kristien HoornaertInge VereeckeChantal DewinterThomas RosenbergFrits A BeemerJuliaan LeroyLaila BendixErik BjörckMaryse BonduelleOdile Boute et al.

A1 Journal Article in EUROPEAN JOURNAL OF HUMAN GENETICS

2008

Genotype and phenotype of Stickler syndrome caused by mutations in the COL2A1 gene

Kristien HoornaertChantal DewinterInge VereeckePaul CouckeGeert Mortier

A2 Journal Article in EUROPEAN JOURNAL OF HUMAN GENETICS

2007

A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathies

M MAJAVAKristien HoornaertD BARTHOLDIMC BOUMAK BOUMANM CARRERAK DEVRIENDTJ HURSTG KITSOSD NIEDRIST et al.

A1 Journal Article in AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Czech dysplasia metatarsal type: another type II collagen disorder

Kristien HoornaertIvo MarikKazimierz KozlowskiTrevor ColeMartine Le MerrerJuliaan LeroyPaul CouckeDavid SillenceGeert Mortier

A1 Journal Article in EUROPEAN JOURNAL OF HUMAN GENETICS

2006

Form of autosomal dominant spondyloepiphyseal dysplasia is caused by a glycine to alanine substitution in the COL2A1 gene

GS SELLICKKristien HoornaertGeert MortierC KINGCL DOLLINGRA NEWBURY-ECOBM GARGANCM HALLRS HOULSTONSF SMITHSON

A1 Journal Article in CLINICAL DYSMORPHOLOGY

The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene

Kristien HoornaertChantal DewinterInge VereeckeFA BEEMERW COURTENSA FRYERH FRYSSIRAM LEESA MULLNER-EIDENBOCKDL RIMOIN et al.

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

2004

Efficacy of flow- vs impedance-guided autoadjustable continuous positive airway pressure - A randomized cross-over trial

Dirk PevernagiePASCAL PROOTKatrien HertegonneMarleen NeyensKristien HoornaertRomain Pauwels

A1 Journal Article in CHEST