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Journal of the American Academy of Audiology
|
February 8, 2021
Prediction of Behavioral T/C Levels in Cochlear Implant Patients Based Upon Analysis of Electrode Impedances
A Zarowski, A Molisz, E Cardinael, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 31, 2020
Influence of the pre- or postlingual status of cochlear implant recipients on behavioural T/C-levels
A Zarowski, A Molisz, L De Coninck, et al.
AJNR. American Journal of Neuroradiology
|
August 16, 2006
Single-shot, turbo spin-echo, diffusion-weighted imaging versus spin-echo-planar, diffusion-weighted imaging in the detection of acquired middle ear cholesteatoma
B De Foer, J-P Vercruysse, B Pilet, et al.
The American Journal of Otology
|
November 27, 1998
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss
P J Govaerts, G De Ceulaer, K Daemers, et al.
Annals of Human Genetics
|
February 12, 2009
Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients
M Thys, I Schrauwen, K Vanderstraeten, et al.
American Journal of Human Genetics
|
February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36
K Van Den Bogaert, P J Govaerts, I Schatteman, et al.
American Journal of Human Genetics
|
May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24
K Verhoeven, G Van Camp, P J Govaerts, et al.
Bone
|
April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genes
K Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.
Nature Genetics
|
May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
K Verhoeven, L Van Laer, K Kirschhofer, et al.
Page
of 8
Search research articles
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Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Journal of the American Academy of Audiology
|
February 8, 2021
Prediction of Behavioral T/C Levels in Cochlear Implant Patients Based Upon Analysis of Electrode Impedances
A Zarowski, A Molisz, E Cardinael, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 31, 2020
Influence of the pre- or postlingual status of cochlear implant recipients on behavioural T/C-levels
A Zarowski, A Molisz, L De Coninck, et al.
AJNR. American Journal of Neuroradiology
|
August 16, 2006
Single-shot, turbo spin-echo, diffusion-weighted imaging versus spin-echo-planar, diffusion-weighted imaging in the detection of acquired middle ear cholesteatoma
B De Foer, J-P Vercruysse, B Pilet, et al.
The American Journal of Otology
|
November 27, 1998
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss
P J Govaerts, G De Ceulaer, K Daemers, et al.
Annals of Human Genetics
|
February 12, 2009
Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients
M Thys, I Schrauwen, K Vanderstraeten, et al.
American Journal of Human Genetics
|
February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36
K Van Den Bogaert, P J Govaerts, I Schatteman, et al.
American Journal of Human Genetics
|
May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24
K Verhoeven, G Van Camp, P J Govaerts, et al.
Bone
|
April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genes
K Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.
Nature Genetics
|
May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
K Verhoeven, L Van Laer, K Kirschhofer, et al.
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of 8