Tracy Dixon-Salazar

Tracy Dixon-Salazar

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Tracy Dixon-Salazar

Tracy Dixon-Salazar

Publications by authors named "Tracy Dixon-Salazar"

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15Publications

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Reducing placebo exposure in trials: Considerations from the Research Roundtable in Epilepsy.

Neurology 2017 Oct 6;89(14):1507-1515. Epub 2017 Sep 6.

From the Research and New Therapies Program (B.E.F., K.F., J.A.F.), Epilepsy Foundation of America, Landover, MD; Department of Neurology (D.F., J.A.F.), New York University, New York; Department of Neurology (M.B.), Hôpital la Salpêtrière, APHP/ICM, University Pierre et Marie Curie, Paris, France; Cincinnati Children's Research Foundation (T.G.), OH; University of Pennsylvania (J.M.), Philadelphia; LGS Foundation (Lennox-Gastaut Syndrome) (T.D.-S.), Bohemia; Mount Sinai School of Medicine (E.B.), New York, NY; Berry Consultants LLC and University of Central Florida College of Medicine (J.C.), Orlando; Eisai Inc. (J.F.), Woodcliff Lake, NJ; and Department of Neurology (N.B.F.), University of Virginia, Charlottesville.

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http://dx.doi.org/10.1212/WNL.0000000000004535DOI Listing
October 2017

MHC class I limits hippocampal synapse density by inhibiting neuronal insulin receptor signaling.

J Neurosci 2014 Aug;34(35):11844-56

Section of Neurobiology, Division of Biological Sciences, University of California, San Diego, La Jolla, California 92093, Department of Molecular Biology, and Princeton Neuroscience Institute, Princeton University, Princeton, New Jersey 08540

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http://dx.doi.org/10.1523/JNEUROSCI.4642-12.2014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468138PMC
August 2014

Issues related to development of new antiseizure treatments.

Epilepsia 2013 Aug;54 Suppl 4:24-34

Anticonvulsant Drug Development Program, Department of Pharmacology & Toxicology, University of Utah, Salt Lake City, Utah 84108, USA.

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http://dx.doi.org/10.1111/epi.12296DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947404PMC
August 2013

A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS).

Am J Med Genet A 2012 Nov 18;158A(11):2788-96. Epub 2012 Sep 18.

Human Genetics and Genome Research Division, Clinical Genetics Department, National Research Centre, Cairo, Egypt.

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http://dx.doi.org/10.1002/ajmg.a.35583DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3477270PMC
November 2012

Genetic regulation of human brain development: lessons from Mendelian diseases.

Ann N Y Acad Sci 2010 Dec 9;1214:156-67. Epub 2010 Nov 9.

Departments of Neurosciences and Pediatrics, Institute for Genomic Medicine, Howard Hughes Medical Institute, University of California, San Diego, La Jolla, California, USA.

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http://dx.doi.org/10.1111/j.1749-6632.2010.05819.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915827PMC
December 2010

Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria.

Am J Hum Genet 2004 Dec 4;75(6):979-87. Epub 2004 Oct 4.

Laboratory for Neurogenetics, Department of Neurosciences, University of California-San Diego, La Jolla, CA 92093-0691, USA.

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http://dx.doi.org/10.1086/425985DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182159PMC
December 2004

Autism in several members of a family with generalized epilepsy with febrile seizures plus.

J Child Neurol 2004 Aug;19(8):597-603

Division of Biological Sciences, Department of Neurosciences, University of California, San Diego, La Jolla, CA 92093-0624, USA.

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http://dx.doi.org/10.1177/088307380401900806DOI Listing
August 2004