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Fayez Bahmad

Showing results (71-80 of 75) with videos related to

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Neuro-Oncology|May 20, 2016
Extracellular vesicles derived from human vestibular schwannomas associated with poor hearing damage cochlear cellsVitor Y R Soares, Nadia A Atai, Takeshi Fujita, et al.
Brazilian Journal of Otorhinolaryngology|December 18, 2022
Task force Guideline of Brazilian Society of Otology ‒ hearing loss in children - Part I ‒ EvaluationVagner Antonio Rodrigues Silva, Henrique Furlan Pauna, Joel Lavinsky, et al.
Brazilian Journal of Otorhinolaryngology|December 17, 2022
Task force Guideline of Brazilian Society of Otology - hearing loss in children - Part II - TreatmentVagner Antonio Rodrigues Silva, Henrique Furlan Pauna, Joel Lavinsky, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Pendred syndrome in a large consanguineous Brazilian family caused by a homozygous mutation in the SLC26A4 geneAdriana Lofrano-Porto, Gustavo B Barra, Paula P Nascimento, et al.
Auris, Nasus, Larynx|August 13, 2013
A multicenter observational study on the role of comorbidities in the recurrent episodes of benign paroxysmal positional vertigoAlessandro De Stefano, Francesco Dispenza, Hamlet Suarez, et al.
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Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Neuro-Oncology|May 20, 2016
Extracellular vesicles derived from human vestibular schwannomas associated with poor hearing damage cochlear cellsVitor Y R Soares, Nadia A Atai, Takeshi Fujita, et al.
Brazilian Journal of Otorhinolaryngology|December 18, 2022
Task force Guideline of Brazilian Society of Otology ‒ hearing loss in children - Part I ‒ EvaluationVagner Antonio Rodrigues Silva, Henrique Furlan Pauna, Joel Lavinsky, et al.
Brazilian Journal of Otorhinolaryngology|December 17, 2022
Task force Guideline of Brazilian Society of Otology - hearing loss in children - Part II - TreatmentVagner Antonio Rodrigues Silva, Henrique Furlan Pauna, Joel Lavinsky, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Pendred syndrome in a large consanguineous Brazilian family caused by a homozygous mutation in the SLC26A4 geneAdriana Lofrano-Porto, Gustavo B Barra, Paula P Nascimento, et al.
Auris, Nasus, Larynx|August 13, 2013
A multicenter observational study on the role of comorbidities in the recurrent episodes of benign paroxysmal positional vertigoAlessandro De Stefano, Francesco Dispenza, Hamlet Suarez, et al.
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