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Andres Felipe Deik Acosta madiedo, MD

Andres Felipe Deik Acosta madiedo, MD

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Assistant Professor of Clinical Neurology
Department: Neurology

Contact information
Parkinson’s Disease and Movement Disorders Center
Penn Medicine Neuroscience Center
Pennsylvania Hospital
330 South 9th Street,
3rd Floor
Philadelphia, PA 19107
Office: 215-829-7512
Fax: 215-829-6606
M.D. (Medicine)
Universidad del Norte, Barranquilla, Colombia, 2005.
M.S.Ed. (Master in Medical Education)
University of Pennsylvania, 2016.
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Description of Clinical Expertise

Movement Disorders Specialist with interest in dystonia.

Selected Publications

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, December 2014 Notes: doi: 10.1007/s00415-014-7516-3. Epub 2014 Sep 30.

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, May 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, Giladi N, Bressman S, Marder KS.: Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations. Movement Disorders 28(14): 1966-71, December 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, March 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, February 2013 Notes: doi: 10.1016/j.parkreldis.2012.09.007. Epub 2012 Oct 10.

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, September 2012 Notes: pii: tre-02-90-671-1. Epub 2012 (No number for this pub.).

Deik A, Azizi E, Shapira I, Boniece I: Supraclavicular Extraskeletal Myxioid Chondrosarcoma Presenting With a Sensory-Motor Polyneuropathy Associated With Anti-Hu Antibodies. Oncology (Williston Park) 23(8): 718-721, July 2009.

Wanner IB, Deik A, Torres M, Rosendahl A, Neary JT, Lemmon VP, Bixby JL.: A new in vitro model of the glial scar inhibits axon growth. Glia 56(15): 1691-1709, November 2008.

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Last updated: 07/25/2016
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