prof. Els De Leenheer
- ORCID iD
- 0000-0002-2789-3529
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Risk factors for cCMV-related hearing loss
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Risk factors for natural hearing evolution in newborns with congenital cytomegalovirus infection
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Risk Factors for Natural Hearing Evolution in Newborns with Congenital Cytomegalovirus Infection (cCMV)
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Vestibular function in women with Turner syndrome : a pilot study
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Vestibular follow-up program for congenital cytomegalovirus based on 6 years of longitudinal data collection
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Risk factors determining natural hearing evolution in children with congenital cytomegalovirus infection
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Risk factors for hearing loss at birth in newborns with congenital cytomegalovirus infection (cCMV)
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Risk factors determining natural hearing evolution in children with congenital cytomegalovirus infection
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Vestibular infant screening–Flanders : what is the most appropriate vestibular screening tool in hearing-impaired children?
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- Journal Article
- A1
- open access
Negative molecular diagnostics in non-syndromic hearing loss : what next?
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- Journal Article
- A1
- open access
Risk Factors for hearing loss at birth in newborns with congenital cytomegalovirus infection
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- Journal Article
- A1
- open access
Predicting early vestibular and motor function in congenital cytomegalovirus infection
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Predicting the occurrence and functional impact of early vestibular loss in congenital cytomegalovirus infection
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- Conference Paper
- C3
- open access
Predicting the occurrence and functional impact of early vestibular loss in congenital cytomegalovirus infection
(2022) JOURNAL OF VESTIBULAR RESEARCH-EQUILIBRIUM & ORIENTATION. In Journal of Vestibular Research Equilibrium & Orientation 32(Supplement 1). p.S59-S60 -
A 5-year prospective study of vestibular loss in children with congenital cytomegalovirus infection
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- Journal Article
- A1
- open access
Hearing loss in stickler syndrome : an update
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Long-term anatomic and functional outcome of pediatric myringoplasty in primary and revision cases
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Twelve years of neonatal hearing screening : audiological and etiological results
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- Journal Article
- A1
- open access
Three years of vestibular infant screening in infants with sensorineural hearing loss
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Cranial ultrasound and MRI : complementary or not in the diagnostic assessment of children with congenital CMV infection?
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Congenital unilateral hearing loss : characteristics and etiological analysis in 121 patients
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The impact of cochlear implantation on vestibular function in children
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Vestibular function in children with congenital cytomegalovirus infection : 3 years of follow-up
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Results of a multicenter registry for congenital cytomegalovirus infection in Flanders, Belgium : from prenatal diagnosis over neonatal management to therapy
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Vestibular function in children with a congenital cytomegalovirus infection : 3 years of follow-up
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- Journal Article
- A1
- open access
Multidisciplinary approach to the child with sex chromosomal mosaicism including a Y-containing cell line
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Congenital CMV-associated hearing loss : can brain imaging predict hearing outcome?
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Congenital cytomegalovirus infection registry in Flanders : opportunities and pitfalls
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Vestibular function in children with a congenital cytomegalovirus infection : 3 years of follow-up
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Atypical clinical and novel radiological findings in Susac syndrome
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The impact of cleft lip and/or palate on parental quality of life : a pilot study
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Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis
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Ear- and hearing-related impact on quality of life in children with cleft palate : development and pretest of a health-related quality of life (HRQOL) instrument
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The impact of cleft lip and/or palate on parental quality of life : a pilot study
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Vestibular function in children with congenital cytomegalovirus infection : results of 2.5 years of follow-up
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Vestibular function in children with congenital cytomegalovirus infection : results of 2.5 years of follow-up
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- Conference Paper
- C3
- open access
Effect of MRI on distortion product otoacoustic emissions in neonates : a pilot study
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Congenital cytomegalovirus-associated hearing loss : can brain imaging predict hearing outcome?
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Vestibular function in children with congenital cytomegalovirus infection : results of 2.5 years of follow-up
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Vestibular function and motor performance in infants with congenital cytomegalovirus infection : a preliminary study
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Vestibular function in children with a congenital cytomegalovirus infection : results of two years of follow-up
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Vestibular function in children with congenital cytomegalovirus infection : a two-year follow-up
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Comparison of the motor performance and vestibular function in infants with a congenital cytomegalovirus infection or a connexin 26 mutation : a preliminary study
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Cytokine profile of nasal and middle ear polyps in a patient with Woakes' syndrome and eosinophilic otitis media
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Auditory phenotype in Stickler syndrome : results of audiometric analysis in 20 patients
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Motor performance and vestibular function in a congenital cytomegalovirus infection or a connexin 26 mutation
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- Journal Article
- A1
- open access
Laterality and unilateral deafness : patients with congenital right ear deafness do not develop atypical language dominance
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Cephalometrics in Stickler syndrome : objectification of the typical facial appearance
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DNA diagnostics of hereditary hearing loss : a targeted resequencing approach combined with a mutation classification system
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Stickler syndrome: comprehensive clinical and molecular analysis
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Hearing in children with congenital cytomegalovirus infection: results of a longitudinal study
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Early motor development of children with a congenital cytomegalovirus infection
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Motor performance and vestibular function in children diagnosed with congenital cytomegalovirus (cCMV) infection or connexin 26 (Cx26) mutation
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Motorische prestatie en vestibulaire functie bij kinderen gediagnostiseerd met een congenitale cytomegalovirus (cCMV) infectie of een connexine 26 (Cx26) mutatie
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- Conference Paper
- C3
- open access
Cephalometrics in Stickler syndrome: objectification of the typical facial appearance
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- Conference Paper
- C3
- open access
Further delineation of the auditory phenotype in Stickler syndrome
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- Conference Paper
- C3
- open access
Further delineation of the auditory phenotype in Stickler syndrome
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Etiological approach in patients with unidentified hearing loss
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Hearing loss and congenital CMV infection: a systematic review
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Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing
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Diagnostic criteria for Stickler syndrome based on comprehensive clinical and molecular analysis
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A vestibular schwannoma in a patient with Birt-Hogg-Dube syndrome
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- Conference Paper
- C3
- open access
Aetiologies after newborn hearing screening
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Etiological approach in unidentified hearing loss suggestive of a genetic cause
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Audiologic and genetic determination of hearing loss in osteogenesis imperfecta
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Hearing impairment in Stickler syndrome: a systematic review
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Novel COL11A1 mutations in Stickler syndrome detected by next-generation sequencing
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Temporal bone imaging in osteogenesis imperfecta patients with hearing loss
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Specific medical and surgical treatment for chronic inflammatory diseases in children
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- Journal Article
- A1
- open access
Hearing impairment in Stickler syndrome: a systematic review
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- Conference Paper
- C3
- open access
Hearing impairment in children with Stickler syndrome: review of phenotype and correlation with genotype
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Audiological and vestibular findings in congenital cytomegalovirus infection: results of a prospective cohort study
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- Conference Paper
- C3
- open access
Hearing impairment in Stickler syndrome: a systematic review
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Stapes surgery in osteogenesis imperfecta: retrospective analysis of 34 operated ears
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- Conference Paper
- C3
- open access
Temporal bone imaging in osteogenesis imperfecta patients with hearing loss
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- Conference Paper
- C3
- open access
Audiologic and genetic determination of hearing loss in osteogenesis imperfecta
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Association between bone mineral density and hearing loss in osteogenesis imperfecta
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- Journal Article
- A1
- open access
Audiologic phenotype of osteogenesis imperfecta: use in clinical differentiation
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KCNQ4 K⁺ channels tune mechanoreceptors for normal touch sensation in mouse and man
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- Journal Article
- A1
- open access
Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype
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- Conference Paper
- C1
- open access
Association between bone mineral density and hearing loss in osteogenesis imperfecta
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- Conference Paper
- C3
- open access
Stapes surgery in osteogenesis imperfecta: retrospective analysis of 34 operated ears
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- Conference Paper
- C3
- open access
Osteogenesis imperfecta: the audiologic phenotype lacks correlation with the genotype
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Etiological diagnosis in the hearing impaired newborn: proposal of a flow chart
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Cochlear implantation in infants deafened by congenital cytomegalovirus
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Cochlear implants in children deafened bij congenital cytomegalovirus
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Cochlear implants in infants deafened by congenital cytomegalovirus
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Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta
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Destructive otomastoiditis by MRSA from porcine origin
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Management of hearing loss: surgery (incudostapedotomy and malleostapedotomy) and outcome of the procedure
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Stapes surgery in Osteogenesis Imperfecta
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Cochlear implantation in 3 adults with auditory neuropathy/auditory dyssynchrony
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Speech Outcome regarding Overall Intelligibility, Articulation, Resonance and Voice in Flemish Children a Year after Pharyngeal Flap Surgery
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Audiologic and genetic characterization of hearing loss in Osteogenesis Imperfecta
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DFNA2/KCNQ4 and its manifestations.
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A novel mutation identified in the DFNA5 gene in a Dutch family: A clinical and genetic evaluation
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Clinical features of DFNA5
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The phenotype of DFNA13/COL11A2.
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DFNA10/EYA4 - the clinical picture.
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Further delineation of the DFNA5 phenotype: Results of speech recognition tests
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Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness families