MDS Abstracts

Abstracts from the International Congress of Parkinson’s and Movement Disorders.

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2016 International Congress

June 19-23, 2016. Berlin, Germany.

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Thursday, June 23, 2016

12:00pm-1:30pm
Duodenal levodopa infusion: Safety and efficacy in a 6 years outpatient follow-up

S. Simoni, N. Tambasco, E. Sacchini, P. Nigro, F. Ripandelli, P. Calabresi (Perugia, Italy)

Parkinson's disease: Clinical trials, pharmacology and treatment  ·  Exhibit Hall located in Hall B, Level 2
12:00pm-1:30pm
Duodopa treatment experience in Oradea

M. Sabau, L. Botnaru, A. Badea, C. Dudas (Oradea, Romania)

Parkinson's disease: Clinical trials, pharmacology and treatment  ·  Exhibit Hall located in Hall B, Level 2
12:00pm-1:30pm
Duration of levodopa treatment and prevalence of osteoporosis in patients with Parkinson’s disease

S.H. Guptha (Peterborough, United Kingdom)

Other  ·  Exhibit Hall located in Hall B, Level 2
12:00pm-1:30pm
Dynamic prediction for multiple repeated measures and event time data: An application to Parkinson’s disease

S. Luo, J. Wang (Houston, TX, USA)

Parkinson's disease: Clinical trials, pharmacology and treatment  ·  Exhibit Hall located in Hall B, Level 2
12:00pm-1:30pm
Dystonia after peripheral nerve injury in DYT1 transgenic rats

S. Knorr, K. Grundmann-Hauser, J. Volkmann, C.W. Ip (Wuerzburg, Germany)

Dystonia  ·  Exhibit Hall located in Hall B, Level 2
12:00pm-1:30pm
Dystonia-deafness syndrome caused by beta -actin gene mutation and the effect of pallidal deep brain stimulation

H. Eggink, M.E. van Egmond, M.C. Schönherr, C.C. Verschuuren-Bemelmans, T.J. de Koning, M.J.C. van Dijk, M.A.J. Tijssen (Groningen, Netherlands)

Dystonia  ·  Exhibit Hall located in Hall B, Level 2
12:00pm-1:30pm
Dystonia, myoclonus, and tremor without epilepsy associated with a mutation in STXBP1

L.S. Tochen, C. Applegate, H.S. Singer (Baltimore, MD, USA)

Pediatric movement disorder  ·  Exhibit Hall located in Hall B, Level 2
12:00pm-1:30pm
Dystonia, tremor, and dystonic tremor

A.R. Rosen, A.G. Shaikh, H.A. Jinnah (Atlanta, GA, USA)

Dystonia and Pediatric Movement Disorders
12:00pm-1:30pm
DYT16/PRKRA founder mutation causes childhood-onset generalized dystonia in a family from southern Italy

M. Quadri, S. Olgiati, M. Sensi, F. Gualandi, E. Groppo, V. Rispoli, J. Graafland, G.J. Breedveld, G. Fabbrini, A. Berardelli, V. Bonifati (Rotterdam, Netherlands)

Dystonia and Pediatric Movement Disorders
12:00pm-1:30pm
DYT2 dystonia – Too rare to be found?

V. Dobricic, N. Kresojevic, A. Marjanovic, A. Tomic, M. Svetel, I. Novakovic, V. Kostic (Belgrade, Serbia)

Dystonia  ·  Exhibit Hall located in Hall B, Level 2
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