Paul Govaerts
Affiliations: | Universiteit Antwerpen (Belgium) |
Area:
Linguistics Language, Audiology, Speech PathologyGoogle:
"Paul Govaerts"Children
Sign in to add trainee| Kris Van Den Bogaert | grad student | 2004 | Universiteit Antwerpen (Belgium) |
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Publications
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| Tekin AM, de Ceulaer G, Govaerts P, et al. (2020) A New Pathogenic Variant in the TRIOBP Associated with Profound Deafness Is Remediable with Cochlear Implantation. Audiology & Neuro-Otology. 1-9 |
| Battmer RD, Borel S, Brendel M, et al. (2015) Assessment of 'Fitting to Outcomes Expert' FOX™ with new cochlear implant users in a multi-centre study. Cochlear Implants International. 16: 100-9 |
| Buechner A, Vaerenberg B, Gazibegovic D, et al. (2015) Evaluation of the 'Fitting to Outcomes eXpert' (FOX®) with established cochlear implant users. Cochlear Implants International. 16: 39-46 |
| Schauwers K, Coene MMR, Heeren W, et al. (2012) Perception of Pitch Changes in Hearing-Impaired Adults with Aided and Unaided Hearing Loss Journal of Hearing Science. 2012: 25-34 |
| Hilgert N, Huentelman MJ, Thorburn AQ, et al. (2009) Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene. European Journal of Human Genetics : Ejhg. 17: 517-24 |
| Declau F, Van den Bogaert K, Van De Heyning P, et al. (2007) Phenotype-genotype correlations in otosclerosis: clinical features of OTSC2. Advances in Oto-Rhino-Laryngology. 65: 114-8 |
| Govaerts PJ, Daemers K, Yperman M, et al. (2006) Auditory speech sounds evaluation (A§E®): A new test to assess detection, discrminination and identification in hearing impairment Cochlear Implants International. 7: 92-106 |
| Van Den Bogaert K, Govaerts PJ, De Leenheer EM, et al. (2002) Otosclerosis: a genetically heterogeneous disease involving at least three different genes. Bone. 30: 624-30 |
| Van Den Bogaert K, Govaerts PJ, Schatteman I, et al. (2001) A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36. American Journal of Human Genetics. 68: 495-500 |
| Govaerts PJ, De Ceulaer G, Daemers K, et al. (1998) A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss. The American Journal of Otology. 19: 718-23 |