William Hotchkis Richmond Waters

Por Brown, David J
Publicado em 2004

Increased Signal Complexity Improves the Breadth of Generalization in Auditory Perceptual Learning

Por Brown, David J., Proulx, Michael J.
Publicado em 2013

How well do you see what you hear? The acuity of visual-to-auditory sensory substitution

Por Haigh, Alastair, Brown, David J., Meijer, Peter, Proulx, Michael J.
Publicado em 2013

Auditory scene analysis and sonified visual images. Does consonance negatively impact on object formation when using complex sonified stimuli?

Por Brown, David J., Simpson, Andrew J. R., Proulx, Michael J.
Publicado no Front Psychol (2015)

Endoscopic Assisted Removal of a Massive Pediatric Floor of Mouth Dermoid

Por Kovatch, Kevin J, Baerg, Timothy, Ha, Jennifer F, Brown, David J
Publicado no Ear Nose Throat J (2019)

Alternative pathways of zeaxanthin biosynthesis in a Flavobacterium species. Experiments with nicotine as inhibitor

Por McDermott, John C. B., Brown, David J., Britton, George, Goodwin, Trevor W.
Publicado em 1974

Other ways of seeing: From behavior to neural mechanisms in the online “visual” control of action with sensory substitution

Por Proulx, Michael J., Gwinnutt, James, Dell’Erba, Sara, Levy-Tzedek, Shelly, de Sousa, Alexandra A., Brown, David J.
Publicado no Restor Neurol Neurosci (2015)

Mathematical Model Developed for Environmental Samples: Prediction of GC/MS Dioxin TEQ from XDS-CALUX Bioassay Data

Por Brown, David J., Orelien, Jean, Gordon, John D., Chu, Andrew C., Chu, Michael D., Nakamura, Masafumi, Handa, Hiroshi, Kayama, Fujio, Denison, Michael S., Clark, George C.
Publicado em 2007

Autosomal Dominant Stapes Ankylosis with Broad Thumbs and Toes, Hyperopia, and Skeletal Anomalies Is Caused by Heterozygous Nonsense and Frameshift Mutations in NOG, the Gene Encod...

Por Brown, David J., Kim, Theresa B., Petty, Elizabeth M., Downs, Catherine A., Martin, Donna M., Strouse, Peter J., Moroi, Sayoko E., Milunsky, Jeff M., Lesperance, Marci M.
Publicado em 2002

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

Por Bespalova, Irina N., Van Camp, Guy, Bom, Steven J.H., Brown, David J., Cryns, Kim, DeWan, Andrew T., Erson, Ayse E., Flothmann, Kris, Kunst, Henricus P.M., Kurnool, Purnima, Sivakumaran, Theru A., Cremers, Cor W.R.J., Leal, Suzanne M., Burmeister, Margit, Lesperance, Marci M.
Publicado no Hum Mol Genet (2001)