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R Lang-Roth

Showing results (11-20 of 17) with videos related to

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HNO|September 28, 2006
[Experiments on prosody perception with cochlear implants]H Meister, D Tepeli, P Wagner, et al.
Cochlear Implants International|February 12, 2021
Magnet dislocation following magnetic resonance imaging in cochlear implant users: Diagnostic pathways and managmentL Holtmann, S Hans, F Kaster, et al.
HNO|February 22, 2014
[Quality of universal newborn hearing screening results : Multicenter analysis of data recorded between 2009 and 2012 in four German states]P Matulat, S Fabian, A Köhn, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locusD Bönsch, P Scheer, C Neumann, et al.
Clinical Genetics|November 4, 2016
Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1)C Neuhaus, R Lang-Roth, U Zimmermann, et al.
HNO|October 17, 2006
[Diagnosis and therapy of auditory synaptopathy/neuropathy]T Moser, N Strenzke, A Meyer, et al.
HNO|March 11, 2014
[Universal newborn hearing screening : Definition of uniform parameters by the Association of German Hearing Screening Centers as a requirement for nationwide evaluation with valid results]I Brockow, M Praetorius, K Neumann, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
HNO|September 28, 2006
[Experiments on prosody perception with cochlear implants]H Meister, D Tepeli, P Wagner, et al.
Cochlear Implants International|February 12, 2021
Magnet dislocation following magnetic resonance imaging in cochlear implant users: Diagnostic pathways and managmentL Holtmann, S Hans, F Kaster, et al.
HNO|February 22, 2014
[Quality of universal newborn hearing screening results : Multicenter analysis of data recorded between 2009 and 2012 in four German states]P Matulat, S Fabian, A Köhn, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locusD Bönsch, P Scheer, C Neumann, et al.
Clinical Genetics|November 4, 2016
Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1)C Neuhaus, R Lang-Roth, U Zimmermann, et al.
HNO|October 17, 2006
[Diagnosis and therapy of auditory synaptopathy/neuropathy]T Moser, N Strenzke, A Meyer, et al.
HNO|March 11, 2014
[Universal newborn hearing screening : Definition of uniform parameters by the Association of German Hearing Screening Centers as a requirement for nationwide evaluation with valid results]I Brockow, M Praetorius, K Neumann, et al.
Pageof 2