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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
MD (Medicine)
Universidad del Norte, Barranquilla, Colombia, 2005.
Permanent link
Perelman School of Medicine > Faculty > Search

Description of Clinical Expertise

Movement Disorders Specialist with interest in dystonia.

Selected Publications

Miravite J, Deik A, Swan M, Sarva H, Kopell BH, Severt WL: Parkinsonism and dystonia in Lubag disease respond well to high pulse width/low-frequency Globus Pallidus interna deep brain stimulation. Neurology: Clinical Practice March 2015 Notes: Epub ahead of print.

Sarva H, Deik A, Swan M and Severt L.: Freezing of gait after a thalamic hemorrhage can respond to venlafaxine and rivastigmine. Neurology: Clinical Practice January 2015 Notes: Published online before print January 2015.

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.

Smith K, Deik A, Stern M, Thompson P: Undulating lingual dyskinesia with symptomatic palatal tremor and inferior olivary hypertrophy following cerebellar hemisphere hematoma. Movement Disorders Clinical Practice 1(3): 245-246, September 2014.

Deik A and Saunders-Pullman R: Atypical presentation of Late-Onset Tay-Sachs Disease. Muscle and Nerve 49(5): 768-71, May 2014 Notes: Epub ahead of print.

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, 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 March 2013 Notes: [Epub ahead of print]

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.

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Last updated: 11/18/2015
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