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Presse Medicale (Paris, France : 1983)|November 2, 2017
[Genetic hearing loss]Lei Tanaka-Ouyang, Sandrine Marlin, Jérôme Nevoux
Advances in Experimental Medicine and Biology|December 30, 2019
Genetic Deciphering of Early-Onset and Severe Retinal Dystrophy Associated with Sensorineural Hearing LossSabrina Mechaussier, Sandrine Marlin, Josseline Kaplan, et al.
The Annals of Otology, Rhinology, and Laryngology|January 15, 2015
Pediatric cochlear implantation in residual hearing candidatesMaxime Gratacap, Briac Thierry, Isabelle Rouillon, et al.
International Journal of Pediatric Otorhinolaryngology|August 7, 2009
Mycophenolate mofetil as a treatment of steroid dependent Cogan's syndrome in childhoodCharlotte Hautefort, Natalie Loundon, Marta Montchilova, et al.
European Journal of Medical Genetics|September 6, 2011
Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotypeLaurence Jonard, Vincent Couloigner, Sébastien Pierrot, et al.
Human Mutation|February 4, 2010
Review and update of mutations causing Waardenburg syndromeVéronique Pingault, Dorothée Ente, Florence Dastot-Le Moal, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 7, 2003
Usher syndrome and cochlear implantationNatalie Loundon, Sandrine Marlin, Denise Busquet, et al.
International Journal of Pediatric Otorhinolaryngology|February 20, 2008
Cochlear implant and inner ear malformation. Proposal for an hyperosmolar therapy at surgeryNatalie Loundon, Nicolas Leboulanger, Janine Maillet, et al.
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