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H P Zenner

Showing results (241-250 of 255) with videos related to

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Oncology|January 1, 1985
Recombinant interferon-alpha-2C in laryngeal papillomatosis: preliminary results of a prospective multicentre trialH P Zenner, W Kley, P Clarós, et al.
HNO|November 1, 2000
[Mutational analysis of the connexin26 gene in sporadic cases of moderate to profound deafness]S Kupka, F Mirghomizadeh, T Haug, et al.
FEBS Letters|March 10, 1997
Desensitization of the P2X(2) receptor controlled by alternative splicingU Brändle, P Spielmanns, R Osteroth, et al.
Otolaryngologia Polska = the Polish Otolaryngology|May 18, 2001
[An attempt to identify the most frequent genomic mutations responsible for isolated deafness in patients after cochlear implantation]W Szyfter, A Pruszewicz, H P Zenner, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9S M Leal, F Apaydin, C Barnwell, et al.
FEBS Letters|November 20, 1995
Subunit-specific inhibition of inward-rectifier K+ channels by quinidineT Doi, B Fakler, J H Schultz, et al.
Human Mutation|October 17, 2006
Deficient membrane integration of the novel p.N14D-GJB2 mutant associated with non-syndromic hearing impairmentB Haack, K Schmalisch, M Palmada, et al.
Journal of Neurobiology|February 18, 1999
Distinct thyroid hormone-dependent expression of TrKB and p75NGFR in nonneuronal cells during the critical TH-dependent period of the cochleaM Knipper, L Gestwa, W J Ten Cate, et al.
HNO|July 17, 1999
[Hearing loss caused by leisure noise]H P Zenner, V Struwe, G Schuschke, et al.
HNO|June 10, 2015
[On the interdisciplinary S3 guidelines for the treatment of chronic idiopathic tinnitus]H-P Zenner, W Delb, B Kröner-Herwig, et al.
Pageof 26

Showing results (241-250 of 255) with videos related to

Sort By:
Pageof 26
Oncology|January 1, 1985
Recombinant interferon-alpha-2C in laryngeal papillomatosis: preliminary results of a prospective multicentre trialH P Zenner, W Kley, P Clarós, et al.
HNO|November 1, 2000
[Mutational analysis of the connexin26 gene in sporadic cases of moderate to profound deafness]S Kupka, F Mirghomizadeh, T Haug, et al.
FEBS Letters|March 10, 1997
Desensitization of the P2X(2) receptor controlled by alternative splicingU Brändle, P Spielmanns, R Osteroth, et al.
Otolaryngologia Polska = the Polish Otolaryngology|May 18, 2001
[An attempt to identify the most frequent genomic mutations responsible for isolated deafness in patients after cochlear implantation]W Szyfter, A Pruszewicz, H P Zenner, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9S M Leal, F Apaydin, C Barnwell, et al.
FEBS Letters|November 20, 1995
Subunit-specific inhibition of inward-rectifier K+ channels by quinidineT Doi, B Fakler, J H Schultz, et al.
Human Mutation|October 17, 2006
Deficient membrane integration of the novel p.N14D-GJB2 mutant associated with non-syndromic hearing impairmentB Haack, K Schmalisch, M Palmada, et al.
Journal of Neurobiology|February 18, 1999
Distinct thyroid hormone-dependent expression of TrKB and p75NGFR in nonneuronal cells during the critical TH-dependent period of the cochleaM Knipper, L Gestwa, W J Ten Cate, et al.
HNO|July 17, 1999
[Hearing loss caused by leisure noise]H P Zenner, V Struwe, G Schuschke, et al.
HNO|June 10, 2015
[On the interdisciplinary S3 guidelines for the treatment of chronic idiopathic tinnitus]H-P Zenner, W Delb, B Kröner-Herwig, et al.
Pageof 26