Showing results (1171-1180 of 1,596) with videos related to

Sort By:
Pageof 160
Pigment Cell Research|September 13, 2006
Dopaquinone redox exchange with dihydroxyindole and dihydroxyindole carboxylic acidR Edge, M d'Ischia, E J Land, et al.
The Laryngoscope|June 5, 2007
Cochlear implantation in the neurofibromatosis type 2 patient: long-term follow-upBrian A Neff, R Mark Wiet, John M Lasak, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 29, 2005
Device nonuse among adult cochlear implant recipientsY M Bhatt, K M J Green, D J Mawman, et al.
Journal of Medical Genetics|February 20, 2007
Mosaicism in neurofibromatosis type 2: an update of risk based on uni/bilaterality of vestibular schwannoma at presentation and sensitive mutation analysis including multiple ligation-dependent probe amplificationD Gareth R Evans, R T Ramsden, A Shenton, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 18, 2021
Predictive In Vitro-In Vivo Extrapolation for Time Dependent Inhibition of CYP1A2, CYP2C8, CYP2C9, CYP2C19, and CYP2D6 Using Pooled Human Hepatocytes, Human Liver Microsomes, and a Simple Mechanistic Static ModelDiane Ramsden, Elke S Perloff, Andrea Whitcher-Johnstone, et al.
Antimicrobial Agents and Chemotherapy|October 15, 2014
Mass balance, metabolite profile, and in vitro-in vivo comparison of clearance pathways of deleobuvir, a hepatitis C virus polymerase inhibitorLin-Zhi Chen, John P Sabo, Elsy Philip, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|December 25, 2002
Meningitis following cochlear implantation: pathomechanisms, clinical symptoms, conservative and surgical treatmentsW Arnold, G Bredberg, W Gstöttner, et al.
Genes, Brain, and Behavior|November 17, 2007
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairmentM Falcaro, A Pickles, D F Newbury, et al.
Journal of Medical Genetics|December 1, 1992
A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severityD G Evans, S M Huson, D Donnai, et al.
Methods in Enzymology|March 11, 2018
High-Throughput Analysis of DNA Break-Induced Chromosome Rearrangements by Amplicon SequencingAlexander J Brown, Aneesa T Al-Soodani, Miles Saul, et al.
Pageof 160