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S Marlin

Showing results (41-50 of 73) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 15, 2005
Auditory neuropathy or endocochlear hearing loss?N Loundon, A Marcolla, I Roux, et al.
Neurology India|October 9, 2015
Neuromodulation as a last resort option in the treatment of chronic daily headaches in patients with idiopathic intracranial hypertensionAndrew B Shaw, Mayur Sharma, Ammar Shaikhouni, et al.
FEBS Letters|December 31, 2002
Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafnessR Bruzzone, V Veronesi, D Gomès, et al.
Cell|February 20, 1999
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafnessC Kubisch, B C Schroeder, T Friedrich, et al.
Delaware Medical Journal|May 1, 1988
Doctor-patient arbitration: a proposal whose time has comeF S Babiarz, P B Bartoshesky, V F Battaglia, et al.
Clinical Genetics|November 26, 2009
Phenotype and genotype in females with POU3F4 mutationsS Marlin, M P Moizard, A David, et al.
AJNR. American Journal of Neuroradiology|December 15, 2012
Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutationsM Elmaleh-Bergès, C Baumann, N Noël-Pétroff, et al.
International Journal of Pediatric Otorhinolaryngology|October 18, 2005
Results of cochlear implantation in two children with mutations in the OTOF geneI Rouillon, A Marcolla, I Roux, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|September 29, 2012
[Prenatal diagnosis of cleft lip with or without cleft palate: retrospective study and review]A Guyot, V Soupre, M-P Vazquez, et al.
Journal of Medical Genetics|May 9, 2006
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%A-F Roux, V Faugère, S Le Guédard, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 15, 2005
Auditory neuropathy or endocochlear hearing loss?N Loundon, A Marcolla, I Roux, et al.
Neurology India|October 9, 2015
Neuromodulation as a last resort option in the treatment of chronic daily headaches in patients with idiopathic intracranial hypertensionAndrew B Shaw, Mayur Sharma, Ammar Shaikhouni, et al.
FEBS Letters|December 31, 2002
Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafnessR Bruzzone, V Veronesi, D Gomès, et al.
Cell|February 20, 1999
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafnessC Kubisch, B C Schroeder, T Friedrich, et al.
Delaware Medical Journal|May 1, 1988
Doctor-patient arbitration: a proposal whose time has comeF S Babiarz, P B Bartoshesky, V F Battaglia, et al.
Clinical Genetics|November 26, 2009
Phenotype and genotype in females with POU3F4 mutationsS Marlin, M P Moizard, A David, et al.
AJNR. American Journal of Neuroradiology|December 15, 2012
Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutationsM Elmaleh-Bergès, C Baumann, N Noël-Pétroff, et al.
International Journal of Pediatric Otorhinolaryngology|October 18, 2005
Results of cochlear implantation in two children with mutations in the OTOF geneI Rouillon, A Marcolla, I Roux, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|September 29, 2012
[Prenatal diagnosis of cleft lip with or without cleft palate: retrospective study and review]A Guyot, V Soupre, M-P Vazquez, et al.
Journal of Medical Genetics|May 9, 2006
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%A-F Roux, V Faugère, S Le Guédard, et al.
Pageof 8