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M Tekin

Showing results (71-80 of 92) with videos related to

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Human Genetics|June 21, 2001
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in CaucasiansM Tekin, N Akar, S Cin, et al.
The Journal of Craniofacial Surgery|November 26, 2024
Next-generation Robotics in Otology: The HEARO ProcedureAhmet M Tekin, Ronald L A W Bleys, Marco Matulic, et al.
Genes|March 29, 2023
Evaluation of a Less Invasive Cochlear Implant Surgery in <i>OPA1</i> Mutations Provoking DeafblindnessAhmet M Tekin, Hermine Baelen, Emilie Heuninck, et al.
Clinical Genetics|December 31, 2013
Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstructionJ Foster, S Kapoor, O Diaz-Horta, et al.
Minerva Pediatrica|September 18, 2015
Attention deficit and hyperactivity disorder and infantile colicN Kaymaz, M E Uzun, S Cevizci, et al.
Rheumatology (Oxford, England)|February 9, 2000
Genotype-phenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosisF Yalçinkaya, N Cakar, M Misirlioğlu, et al.
The Journal of Craniofacial Surgery|August 21, 2023
Effectiveness of Training: Airway Management of Tracheostomized Pediatric Patients by Pediatric Residents and Anesthesiology ResidentsYasar Kemal Duymaz, Furkan Bayram, Şamil Şahin, et al.
Genes|April 30, 2021
A New Pathogenic Variant in <i>POU3F4</i> Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative SurgeryAhmet M Tekin, Marco Matulic, Wim Wuyts, et al.
Frontiers in Neurology|April 7, 2022
First Study in Men Evaluating a Surgical Robotic Tool Providing Autonomous Inner Ear Access for Cochlear ImplantationVedat Topsakal, Emilie Heuninck, Marco Matulic, et al.
Clinical Genetics|April 8, 2014
A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiationK O Yariz, Y B Sakalar, X Jin, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Human Genetics|June 21, 2001
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in CaucasiansM Tekin, N Akar, S Cin, et al.
The Journal of Craniofacial Surgery|November 26, 2024
Next-generation Robotics in Otology: The HEARO ProcedureAhmet M Tekin, Ronald L A W Bleys, Marco Matulic, et al.
Genes|March 29, 2023
Evaluation of a Less Invasive Cochlear Implant Surgery in <i>OPA1</i> Mutations Provoking DeafblindnessAhmet M Tekin, Hermine Baelen, Emilie Heuninck, et al.
Clinical Genetics|December 31, 2013
Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstructionJ Foster, S Kapoor, O Diaz-Horta, et al.
Minerva Pediatrica|September 18, 2015
Attention deficit and hyperactivity disorder and infantile colicN Kaymaz, M E Uzun, S Cevizci, et al.
Rheumatology (Oxford, England)|February 9, 2000
Genotype-phenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosisF Yalçinkaya, N Cakar, M Misirlioğlu, et al.
The Journal of Craniofacial Surgery|August 21, 2023
Effectiveness of Training: Airway Management of Tracheostomized Pediatric Patients by Pediatric Residents and Anesthesiology ResidentsYasar Kemal Duymaz, Furkan Bayram, Şamil Şahin, et al.
Genes|April 30, 2021
A New Pathogenic Variant in <i>POU3F4</i> Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative SurgeryAhmet M Tekin, Marco Matulic, Wim Wuyts, et al.
Frontiers in Neurology|April 7, 2022
First Study in Men Evaluating a Surgical Robotic Tool Providing Autonomous Inner Ear Access for Cochlear ImplantationVedat Topsakal, Emilie Heuninck, Marco Matulic, et al.
Clinical Genetics|April 8, 2014
A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiationK O Yariz, Y B Sakalar, X Jin, et al.
Pageof 10