Selected Publications:
Sarva H, Miravite J, Swan MC, Deik A, Raymond D, Severt WL, Kopell BH: A Case of Myoclonus-Dystonia Responding to Low-frequency Pallidal Stimulation Tremor Other Hyperkinet Mov (N Y) 5 (7): 460,2017.
Matthew Swan, Nancy Doan, Robert A. Ortega, Matthew Barrett,
William Nichols, Laurie Ozelius, Jeannie Soto-Valencia, Sarah Boschung, Andres Deik, Harini Sarva, Jose Cabassa, Brooke Johannes, Deborah Raymond, Karen Marder, Nir Giladi, Joan Miravite, William Severt, Rivka Sachdev, Vicki Shanker,
Susan Bressman, Rachel Saunders-Pullman: Neuropsychiatric characteristics of GBA-associated Parkinson disease Journal of the Neurological Sciences (370): 63-69,2016.
Loaiza-Bonilla A, Jensen CE, Shroff S, Furth E, Bonilla-Reyes PA, Deik AF, Morrissette J: KDR Mutation as a Novel Predictive Biomarker of Exceptional Response to Regorafenib in Metastatic Colorectal Cancer Cureus 3 (8 (2)): e478,2016.
Loaiza-Bonilla A, Jensen CE, Shroff S, Furth E, Bonilla-Reyes PA, Deik AF, Morrissette J.: KDR Mutation as a Novel Predictive Biomarker of Exceptional Response to Regorafenib in Metastatic Colorectal Cancer Cureus 8 (2): 2016.
Deik A, Johannes B, Rucker JC, Sánchez E, Brodie SE, Deegan E, Landy K, Kajiwara Y, Scelsa S, Saunders-Pullman R, Paisán-Ruiz C.
: Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia Journal of Neurology 261 (12): 2411-23,2014.
Saunders-Pullman R, Fuchs T, San Luciano M, Raymond D, Brashear A, Ortega R, Deik A, Ozelius L, Bressman SB: Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.
Movement Disorders 29 (6): 812-8,2014.
Alcalay RN, Mirelman A, Saunders-Pullman R, Tang MX, Mejia Santana H, Raymond D, Roos E, Orbe-Reilly M, Gurevich T, Bar Shira A, Gana Weisz M, Yasinovsky K, Zalis M, Thaler A, Deik A, Barrett MJ, Cabassa J, Groves M, Hunt AL, Lubarr N, San Luciano M, Miravite J, Palmese C, Sachdev R, Sarva H, Severt L, Shanker V, Swan MC, Soto-Valencia J, Johannes B, Ortega R, Fahn S, Cote L, Waters C, Mazzoni P, Ford B, Louis E, Levy O, Rosado L, Ruiz D, Dorovski T, Pauciulo M, Nichols W, Orr-Urtreger A, Ozelius L, Clark L: Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations.
Movement Disorders 28 (14): 1966-71,2013.
Gan-Or Z, Ozelius LJ, Bar-Shira A, Saunders-Pullman R, Mirelman A, Kornreich R, Gana-Weisz M, Raymond D, Rozenkrantz L, Deik A, Gurevich T, Gross SJ, Schreiber-Agus N, Giladi N, Bressman SB, Orr-Urtreger A: The p.L302P Mutation in the Lysosomal Enzyme Gene SMPD1 is a Risk Factor for Parkinson Disease. Neurology 80 (17): 1606-10,2013.
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.
Deik AF, O'Riordan S, Luciano MS, Shanker VL, Raymond D, Bressman SB, Saunders-Pullman R: Spatial Discrimination Threshold Abnormalities are not Detected in a Pilot Study of DYT6 Dystonia Mutation Carriers Tremor Other Hyperkinet Mov (N Y) 2 : 2012.
View all publications