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Risk factors for natural hearing evolution in newborns with congenital cytomegalovirus infection
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Risk factors for cCMV-related hearing loss
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Risk factors determining natural hearing evolution in children with congenital cytomegalovirus infection
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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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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 for Natural Hearing Evolution in Newborns with Congenital Cytomegalovirus Infection (cCMV)
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Twelve years of neonatal hearing screening : audiological and etiological results
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- Journal Article
- A1
- open access
Hearing loss in stickler syndrome : an update
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Congenital CMV-associated hearing loss : can brain imaging predict hearing outcome?
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Congenital unilateral hearing loss : characteristics and etiological analysis in 121 patients
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Congenital cytomegalovirus-associated hearing loss : can brain imaging predict hearing outcome?
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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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Auditory phenotype in Stickler syndrome : results of audiometric analysis in 20 patients
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Stickler syndrome: comprehensive clinical and molecular analysis
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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
Cephalometrics in Stickler syndrome: objectification of the typical facial appearance
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Etiological approach in patients with unidentified hearing loss
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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
Aetiologies after newborn hearing screening
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Diagnostic criteria for Stickler syndrome based on comprehensive clinical and molecular analysis
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Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing
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Etiological approach in unidentified hearing loss suggestive of a genetic cause
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Novel COL11A1 mutations in Stickler syndrome detected by next-generation sequencing
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Hearing impairment in Stickler syndrome: a systematic review
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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 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