Description of Research Expertise:
Site principal investigator for clinical trials in Movement Disorders.
Selected Publications:
Mariel Pullman, Roberto Ortega, Amanda Glickman, Andres Deik, Deborah Raymond, Karen Marder, Nir Giladi, Susan Bressman, Johann Hagenah, Norbert Bruggemann, Rachel Saunders-Pullman: Increased substantia nigra echogenicity in LRRK2 family members without mutations. Movement Disorders : 2018.
Coughlin David, Bardakjian Tanya, Spindler Meredith, Deik Andres: Hereditary Myoclonus Dystonia: A Novel SGCE Mutation and Phenotype Including Intellectual Disability. Tremor and other hyperkinetic movements (New York, N.Y.) : 2018.
Sarva Harini, Miravite Joan, Swan Matthew C, Deik Andres, Raymond Deborah, Severt William Lawrence, Kopell Brian H: A Case of Myoclonus-Dystonia Responding to Low-frequency Pallidal Stimulation. Tremor and other hyperkinetic movements (New York, N.Y.) 7 : 460,2017.
Swan Matthew, Doan Nancy, Ortega Robert A, Barrett Matthew, Nichols William, Ozelius Laurie, Soto-Valencia Jeannie, Boschung Sarah, Deik Andres, Sarva Harini, Cabassa Jose, Johannes Brooke, Raymond Deborah, Marder Karen, Giladi Nir, Miravite Joan, Severt William, Sachdev Rivka, Shanker Vicki, Bressman Susan, Saunders-Pullman Rachel: Neuropsychiatric characteristics of GBA-associated Parkinson disease. Journal of the neurological sciences 370 : 63-69,2016.
Loaiza-Bonilla Arturo, Jensen Christopher E, Shroff Stuti, Furth Emma, Bonilla-Reyes Paula A, Deik Andres F, Morrissette Jennifer: KDR Mutation as a Novel Predictive Biomarker of Exceptional Response to Regorafenib in Metastatic Colorectal Cancer. Cureus 8 (2): e478,2016.
Sarva Harini, Deik Andres, Swan Matthew Carrington, Severt William Lawrence: Freezing of gait after a hemorrhagic stroke can respond to venlafaxine and rivastigmine. Neurology. Clinical practice 5 (3): 267-269,2015.
Deik Andres, Johannes Brooke, Rucker Janet C, Brodie Scott E, Deegan Erin, Landy Kathryn, Scelsa Stephen, Saunders-Pullman Rachel, Paisan-Ruiz Coro: Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia. Journal of Neurology 261 (12): 2411-23,2014.
Saunders-Pullman Rachel, Fuchs Tania, San Luciano Marta, Raymond Deborah, Brashear Alison, Ortega Robert, Deik Andres, Ozelius Laurie J, Bressman Susan B: Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites. Movement disorders : official journal of the Movement Disorder Society 29 (6): 812-8,2014.
Deik Andres, Saunders-Pullman Rachel: Atypical presentation of late-onset Tay-Sachs disease. Muscle & nerve 49 (5): 768-71,2014.
Barrett MJ, Hagenah J, Dhawan V, Deik A, Stanley K, Raymond D, Ozelius LJ, Gross, S, Schrieber-Agus Eidelberg D, Mirelman A, Marder K, Bressman SB, Saunders-Pullman R and the LRRK2 AJ Consortium: Transcranial Sonography and Functional Imaging in Glucocerebrosidase Mutation Associated in Parkinson Disease. Parkinsonism and Related Disorders 19 (2): 186-191,2013.
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