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Mahmut Tayyar Kalcioglu

Showing results (31-40 of 39) with videos related to

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The Journal of International Advanced Otology|April 10, 2025
Progressive Ototoxicity of Baby Shampoo As An Antifog Agent: An Experimental StudyAhmet Mutlu, Burcu Bakici, Ayşe Yasemin Gunduz, et al.
Audiology Research|March 24, 2026
New Insight into Potential Otoprotective Effects of Lactoferrin: Is It Paradoxically Ototoxic? An Experimental InvestigationAhmet Mutlu, Ayse Yasemin Gunduz, Burcu Bakici, et al.
Northern Clinics of Istanbul|January 29, 2019
Ear atresia: Is there a role of apoptosis-regulating miRNAs?Ezgi Aslan, Emre Akbas, Sena Yilmaz, et al.
Sisli Etfal Hastanesi Tip Bulteni|July 10, 2026
In Vitro Antimicrobial Activity of Five Turkish Honey Types Against Otitis Externa Pathogens: A Comparative StudySerdal Celik, Hamdi Sirac Gundogdu, Nihat Arda Buyukasik, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing lossDuygu Duman, Memoona Ramzan, Asli Subasioglu, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.
American Journal of Otolaryngology|August 22, 2024
Efficacy and safety of SENS-401 in sudden sensorineural hearing loss: The AUDIBLE-S randomized placebo-controlled phase IIb trialItzhak Braverman, Maya Elziere, Zoran Komazec, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|August 29, 2020
A novel approach to managing COVID-19 patients; results of lopinavir plus doxycycline cohortYasemin Cag, Sacit Icten, Burcu Isik-Goren, et al.
Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
The Journal of International Advanced Otology|April 10, 2025
Progressive Ototoxicity of Baby Shampoo As An Antifog Agent: An Experimental StudyAhmet Mutlu, Burcu Bakici, Ayşe Yasemin Gunduz, et al.
Audiology Research|March 24, 2026
New Insight into Potential Otoprotective Effects of Lactoferrin: Is It Paradoxically Ototoxic? An Experimental InvestigationAhmet Mutlu, Ayse Yasemin Gunduz, Burcu Bakici, et al.
Northern Clinics of Istanbul|January 29, 2019
Ear atresia: Is there a role of apoptosis-regulating miRNAs?Ezgi Aslan, Emre Akbas, Sena Yilmaz, et al.
Sisli Etfal Hastanesi Tip Bulteni|July 10, 2026
In Vitro Antimicrobial Activity of Five Turkish Honey Types Against Otitis Externa Pathogens: A Comparative StudySerdal Celik, Hamdi Sirac Gundogdu, Nihat Arda Buyukasik, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing lossDuygu Duman, Memoona Ramzan, Asli Subasioglu, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.
American Journal of Otolaryngology|August 22, 2024
Efficacy and safety of SENS-401 in sudden sensorineural hearing loss: The AUDIBLE-S randomized placebo-controlled phase IIb trialItzhak Braverman, Maya Elziere, Zoran Komazec, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|August 29, 2020
A novel approach to managing COVID-19 patients; results of lopinavir plus doxycycline cohortYasemin Cag, Sacit Icten, Burcu Isik-Goren, et al.
Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.
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