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15th INTERNATIONAL CONGRESS OF PARKINSON'S

15th INTERNATIONAL CONGRESS OF PARKINSON'S

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Abstracts by Topic<br />

Ataxia<br />

1 Genetic, biochemical and genotoxicity investigations on Cuban<br />

families affected by spinocerebellar ataxia type 2<br />

L.E. Almaguer-Mederos, R. Aguilera-Rodríguez, Y. González Zaldívar,<br />

D. Almaguer-Gotay, D. Cuello-Almarales, A. Álvarez Sosa, J. Laffita-<br />

Mesa, G. Sánchez Cruz, J. Montes-Brown, S. Mejías Brito, G. Ávila<br />

Ávila, Y. Vázquez-Mojena, P. Zayas-Feria, A. Estupiñán-Rodríguez,<br />

P. Bahr-Valcárcel, J. Aguiar-Santiago, G. Auburger (Holguín, Cuba)<br />

2 Urinary symptoms and urodynamic findings in patients with<br />

Machado-Joseph disease<br />

A.F.A. Musegante, P.N.S. Almeida, A.L. Barboza, U. Barroso,<br />

Jr. (Salvador, Bahia, Brazil)<br />

3 Tremor-spectrum in spinocerebellar ataxia type 3 (SCA3)<br />

C. Bonnet, E. Apartis, M. Anheim, A.P. Legrand, F. Baizabal-Carvallo,<br />

A.M. Bonnet, A. Durr, M. Vidailhet (Praha, Czech Republic)<br />

4 Cognitive deficits and spinocerebellar ataxia type 3: A model to study<br />

the cerebellar cognitive affective syndrome hypothesis?<br />

P. Braga-Neto, J.L. Pedroso, H. Alessi, A.C. Felício, L.A. Dutra,<br />

P. Weisman, R.F. Santos-Galduroz, P.H.F. Bertolucci, A.A. Gabbai,<br />

O.G.P. Barsottini (São Paulo, Brazil)<br />

5 Dysarthria in patients with Friedreich’s ataxia and spinocerebellar<br />

ataxia<br />

B. Brendel, T. Schölderle, T. Lindig, M. Synofzik, L. Schöls,<br />

H. Ackermann, W. Ziegler (Tübingen, Germany)<br />

6 The clinical spectrum of ataxia with oculomotor apraxia type 2<br />

(AOA2)<br />

F. Brugger, G. Kägi, H. You, A. Kaelin-Lang, M. Koenig, J.-P. Delaunoy,<br />

M. Schüpbach (St. Gallen, Switzerland)<br />

7 Frequency of spinocerebellar ataxia type 3 (SCA3) or Machado<br />

Joseph disease in a Peruvian population<br />

M.R. Cornejo, C. Timaná, R.D. Chacón, O.G. Ortega, V.M. Marca,<br />

G. Torres, L. Torres, C.A. Cosentino, M.B. Flores, P.E. Mazzetti (Lima,<br />

Peru)<br />

8 Friedreich ataxia gene in Cuban population<br />

T. Cruz-Mariño, Y. González-Zaldivar, J.M. Laffita-Mesa,<br />

L.E. Almaguer-Mederos, R. Aguilera-Rodríguez, D. Alaguer-Gotay,<br />

R. Rodríguez-Labrada, R. Rodríguez-Labrada, N. Canales-Ochoa,<br />

P. MacLeod, L. Velázquez-Pérez (Holguín, Cuba)<br />

9 Rehabilitation of multiple sclerosis and Parkinson’s symptoms using<br />

cranial nerve non-invasive neuromodulation (CN-NINM)<br />

Y.P. Danilov, M.E. Tyler, K.A. Kaczmarek (Madison, Wisconsin, USA)<br />

10 Ataxic breathing in Joubert syndrome<br />

M. Fabbri, F. Provini, R. Vetrugno, M. Santucci (Bologna, Italy)<br />

11 FXTAS in patients with Fragile-X gray zone alleles<br />

D. Hall, O. Klepitskaya, F. Tassone, E. Spector, M. Leehey (Chicago,<br />

Illinois, USA)<br />

12 Botulinum toxin-responsive cervical dystonia in spinocerebellar<br />

ataxia type 5<br />

D.J. Houghton, J.M. Ferrara, I. Litvan (Louisville, Kentucky, USA)<br />

15 th <strong>INTERNATIONAL</strong> <strong>CONGRESS</strong> <strong>OF</strong> PARKINSON’S<br />

DISEASE AND MOVEMENT DISORDERS<br />

13 The natural history of spinocerebellar ataxia type 1, 2, 3 and 6: A<br />

2-year follow-up study<br />

H. Jacobi, P. Bauer, P. Giunti, R. Labrum, M.G. Sweeney, P. Charles,<br />

A. Dürr, C. Marelli, C. Globas, C. Linnemann, L. Schöls, M. Rakowicz,<br />

R. Rola, E. Zdzienicka, T. Schmitz-Hübsch, R. Facellu, C. Mariotti,<br />

C. Tomasello, L. Baliko, B. Melegh, A. Filla, C. Rinaldi, B.P. van de<br />

Warrenburg, C.C.P. Verstappen, S. Szymanski, J. Berciano, J. Infante,<br />

D. Timmann, S. Boesch, S. Hering, C. Depondt, M. Pandolfo, J.-<br />

S. Kang, S. Ratzka, J. Schulz, S. Tezenas du Montcel, T. Klockgether<br />

(Bonn, Germany)<br />

14 Normal energy metabolism in spinocerebellar ataxia (SCA) patients<br />

J.-S. Kang, J. Magerkurth, D. Nolte, G. Auburger, U. Pilatus, R. Hilker,<br />

E. Hattingen (Frankfurt/Main, Germany)<br />

15 Visualisation, quantification and correlation of brain atrophy with<br />

clinical symptoms in spinocerebellar ataxias types 1, 2 and 3 using<br />

3D volumetric analysis<br />

S.G.G. Kumar, P.K. Pal, J. Saini, Arvind (Bangalore, India)<br />

16 Delineating the de novo methylation pattern of the ataxin-2<br />

promoter<br />

J.M. Laffita-Mesa, D. Almaguer Gotay, L. Peña-Serrano, B.O. Peter,<br />

D.A. Coello Almarales, V. Kourí (Holguin, Cuba)<br />

17 The contribution of the self PolyQ load [somatic mosaicism] in the<br />

CNS to the onset, disease duration and progression rate of SCA2<br />

J.M. Laffita-Mesa, Y. Vázquez Mojena, D.A. Coello Almarales,<br />

L.C. Velázquez Pérez (Holguin, Cuba)<br />

18 Dynamic postural balance in cerebellar ataxia<br />

P.L.A. Leandro, H.A.G. Teive (Curitiba, Parana, Brazil)<br />

19 GABARAP mRNA expression changes in cerebellar nuclei neurons<br />

after degeneration of GABAergic afferents in Lurcher mutant mice<br />

C. Linnemann, I. Schmeh, C. Schwarz (Tuebingen, Germany)<br />

20 Progressive myoclonic ataxia in coeliac disease despite a well conduct<br />

gluten free diet<br />

C. Marcel, O. Lagha-Boukbiza, J. Perisse, E. Godet, C. Tanchant<br />

(Strasbourg, France)<br />

21 Cerebellar ataxia due to extracerebellar lesions – An MRI<br />

tractography study in six patients<br />

M. Marek, S. Paus, N. Allert, B. Mädler, T. Klockgether, V.A. Coenen<br />

(Bonn, Germany)<br />

22 White matter hyperintensities in a patient with borderline mutation<br />

for spinocerebellar ataxia type 8: A case report<br />

H.P. Moore, W. Sheremata, C. Singer (Miami, Florida, USA)<br />

23 Ataxia severity correlates with Frenchay dysarthrophonia assessment<br />

in Friedreich ataxia<br />

W. Nachbauer, A. Eigentler, J. Rhomberg, I. Ritzer, W. Poewe, S. Boesch<br />

(Innsbruck, Austria)<br />

24 Transcranial sonography in Machado-Joseph disease: Imaging<br />

aspects and correlation with clinical features<br />

J.L. Pedroso, A.C. Felício, P. Braga-Neto, E. Bor-Seng-Shu,<br />

M.J. Teixeira, O.G.P. Barsottini (São Paulo, Brazil)<br />

25 Autosomal recessive ataxias: Frequencies and phenotypes in a large<br />

cohort of patients with early-onset ataxia<br />

J. Schicks, M. Synofzik, C. Schulte, P. Bauer, L. Schöls (, Germany)<br />

26 Cerebellar inhibition in multiple system atrophy patients<br />

Y. Shirota, R. Hanajima, M. Hamada, Y. Terao, H. Matsumoto,<br />

S. Ohminami, R. Tsutsumi, Y. Ugawa (Tokyo, Japan)<br />

TORONTO<br />

85<br />

June 5–9, 2011 Toronto, ON, C anada<br />

Abstracts<br />

by topic

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