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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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C Morales-Angulo

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Acta Otorrinolaringologica Espanola|July 16, 2004

[Evaluation of a family with sensorineural hearing loss due to the Q829X mutation in the OTOF gene]J Gallo-Terán, R Megía López, C Morales-Angulo, et al.

Acta Otorrinolaringologica Espanola|October 14, 2006

[Auditory neuropathy due to the Q829X mutation in the gene encoding otoferlin (OTOF) in an infant screened for newborn hearing impairment]J Gallo-Terán, C Morales-Angulo, N Sánchez, et al.

Acta Otorrinolaringologica Espanola|October 6, 2004

[Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity]J Gallo-Terán, B Arellano, C Morales-Angulo, et al.

European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|July 21, 2017

Analysis of risk factors influencing the outcome of the Epley maneuverE Domínguez-Durán, E Domènech-Vadillo, M G Álvarez-Morujo de Sande, et al.

Journal of Otology|August 31, 2019

Probable benign paroxysmal positional vertigo, spontaneously resolved: Incidence in medical practice, patients' characteristics and the natural courseM G Álvarez-Morujo de Sande, R González-Aguado, G Guerra-Jiménez, et al.

Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|June 16, 2018

Healing criteria: How should an episode of benign paroxistic positional vertigo of posterior semicircular canal's resolution be defined? Prospective observational studyG Guerra-Jiménez, E Domènech-Vadillo, M G Álvarez-Morujo de Sande, et al.

Acta Otorrinolaringologica Espanola|December 16, 2003

[Program of hearing loss early detection in newborn infants in Cantabria. Results of the first year of activities]C Morales Angulo, A González de Aledo Linos, C Bonilla Miera, et al.

Journal of Medical Genetics|August 16, 2003

Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing lossF J del Castillo, M Rodríguez-Ballesteros, Y Martín, et al.

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Showing results (41-50 of 48) with videos related to

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You have reached the last page of results.This site can display upto 48 results.

Acta Otorrinolaringologica Espanola|July 16, 2004

[Evaluation of a family with sensorineural hearing loss due to the Q829X mutation in the OTOF gene]J Gallo-Terán, R Megía López, C Morales-Angulo, et al.

Acta Otorrinolaringologica Espanola|October 14, 2006

[Auditory neuropathy due to the Q829X mutation in the gene encoding otoferlin (OTOF) in an infant screened for newborn hearing impairment]J Gallo-Terán, C Morales-Angulo, N Sánchez, et al.

Acta Otorrinolaringologica Espanola|October 6, 2004

Analysis of risk factors influencing the outcome of the Epley maneuverE Domínguez-Durán, E Domènech-Vadillo, M G Álvarez-Morujo de Sande, et al.

Journal of Otology|August 31, 2019

Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|June 16, 2018

Acta Otorrinolaringologica Espanola|December 16, 2003

[Program of hearing loss early detection in newborn infants in Cantabria. Results of the first year of activities]C Morales Angulo, A González de Aledo Linos, C Bonilla Miera, et al.

Journal of Medical Genetics|August 16, 2003

Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing lossF J del Castillo, M Rodríguez-Ballesteros, Y Martín, et al.

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