2018 International Congress » Ataxia

Date: Sunday, October 7, 2018

Time: 1:45pm-3:15pm

Location: Hall 3FG

Meeting: 2018 International Congress

1:45pm-3:15pm: A clinical and pathological study of small fibers in Friedreich´s Ataxia

E. Indelicato, W. Nachbauer, A. Eigentler, A. Fanciulli, J.P. Ndayisaba, W. Poewe, G. Wenning, J. Wanschitz, S. Boesch (Innsbruck, Austria)

1:45pm-3:15pm: A comparative study on the alterations in the cortical excitability and central motor conduction time in spinocerebellar ataxias 1, 2, 3 and 12

A. Stezin, K. Jhujhunwala, N. Kamble, P. Pal (Bangalore, India)

1:45pm-3:15pm: A comparison of relative displacement by double integration with root mean square in the quantitative evaluation of gait ataxia by triaxial accelerometers

S. Shirai, I. Yabe, M. Matsushima, H. Sasaki (Sapporo, Japan)

1:45pm-3:15pm: A Diagnostic Algorithm for Pediatric Early Onset Ataxia

R. Brandsma, C. Verschuuren, H. Kremer, T. de Koning, M. de Koning-Tijssen, D. Sival (Groningen, Netherlands)

1:45pm-3:15pm: A strategic approach to understand microsatellite repeat loci among Indian spinocerebellar ataxia patients

V. Suroliya, M. Faruq, A. Srivastava (New Delhi, India)

1:45pm-3:15pm: Acute Stroke in Middle Cerebellar Peduncle in a Patient with FXTAS

A. Fraint, D. Hall, R. Dafer (Chicago, IL, USA)

1:45pm-3:15pm: Alterations of cerebello-cortical networks related to the cognitive performance in multiple system atrophy

K. Hara, H. Watanabe, K. Kawabata, E. Bagarinao, R. Ohdake, M. Masuda, T. Yokoi, A. Ogura, T. Tsuboi, M. Ito, M. Katsuno, G. Sobue (Nagoya, Japan)

1:45pm-3:15pm: Antisense FMR1 splice variant: A predictor of fragile X-associated tremor/ataxia syndrome

P. Vittal, S. Pandya, K. Sharp, E. Berry-Kravis, L. Zhou, B. Ouyang, J. Jackson, D. Hall (Winfield, IL, USA)

1:45pm-3:15pm: Ataxia and cerebellar atrophy in Charcot-Marie-Tooth neuropathy type 4C

M. Paucar, H. Skott, K. Samuelsson, H. Malmgren, G. Solders, P. Svenningsson (Stockholm, Sweden)

1:45pm-3:15pm: Case of Friedreich’s ataxia with extremely large repeat expansion without systemic disease

K. Niotis, H. Ellsworth, J. Weaver, H. Sarva (New York, NY, USA)

1:45pm-3:15pm: Cerebellar Ataxia as a Manifestation of Hashimoto Encephalopathy

S. Thakolwiboon, D. Ruthirago, V. Senanarong (Lubbock, TX, USA)

1:45pm-3:15pm: Cerebellar Ataxia case series study from southern Spain: Clinical and molecular description

A. Adarmes Gomez, S. Jesus Maestre, C. Mendez delBarrio, D. Macias Garcia, F. Carrillo Garcia, M. Carballo, P. Gomez Garre, P. Mir Rivera (Seville, Spain)

1:45pm-3:15pm: Cerebello-spinal stimulation in neurodegenerative ataxia: A randomized, double-blind, sham-controlled, crossover trial

A. Benussi, V. Dell'Era, V. Cantoni, E. Bonetta, R. Grasso, R. Manenti, M. Cotelli, A. Padovani, B. Borroni (Brescia, Italy)

1:45pm-3:15pm: Cerebrotendinous Xanthomatosis: A Rare Lipid Storage Disease

H. Hanagasi, G. Yunisova, B. Bilgic, O. Dogu, H. Kaleagasi, Z. Tufekcioglu, E. Lohmann, H. Gurvit, M. Emre (Istanbul, Turkey)

1:45pm-3:15pm: Cervical dystonia priori to ataxia in spinocerebellar ataxia type 3 patients

X.Q. Yuan, R. Dutta, H.F. Shang (Chengdu, China)

1:45pm-3:15pm: Changes detected in swallowing function in Friedreich ataxia over 12 months

M. Keage, M. Delatycki, J. Dyer, L. Corben, A. Vogel (Carlton, Australia)

1:45pm-3:15pm: Changes in balance and gait after a single session of combined cerebellum and primary motor cortex transcranial direct current stimulation (tDCS) in a person with SCA1

M. León, P. Chaná (Santiago, Chile)

1:45pm-3:15pm: Clinical and Molecular Characterization of a Family with Ataxia with Oculomotor Apraxia Type 2

T. Tropea, N. Jain, T. Unger, A. Chen-Plotkin. (Philadelphia, PA, USA)

1:45pm-3:15pm: Clinical and mutation spectrum of Ataxia with oculomotor apraxia-2: An Indian perspective

S. Shakya, M. Faruq, A. Srivastava, I. Singh, A. Garg, R. Rajan, V. Goyal (New Delhi, India)

1:45pm-3:15pm: Clinical characteristics of a family harbouring a novel CCDC88C mutation (SCA40)

W. Nachbauer, E. Indelicato, A. Eigentler, S. Boesch (Innsbruck, Austria)

1:45pm-3:15pm: Clinico-genetic correlation in Indian Spinocerebellar ataxia Type 1 (SCA1) patients

A. Takkar, I. Ahmed, S. Shakya, A. Srivastava (New Delhi, India)

1:45pm-3:15pm: Coexisting CACNA1A pathogenic variant and MJD expansion in the same family

L. Leitão, C. Figueiredo, M. Santos, A.F. Brandão, A. Lopes, J. Sequeiros, I. Alonso, C. Costa (Amadora, Portugal)

1:45pm-3:15pm: Cognitive function impacts gait, functional mobility and falls in Fragile X-Associated Tremor/Ataxia Syndrome

J. O'Keefe, E. Robertson, B. Ouyang, D. Carns, Y. Liu, M. Swanson, B. Bernard, E. Berry-Kravis, D. Hall (Chicago, IL, USA)

1:45pm-3:15pm: Comorbid Pediatric Early Onset Ataxia and Dystonia – Is the Cerebellum Involved?

D. Sival, M. Tijssen, D. Verbeek (Groningen, Netherlands)

1:45pm-3:15pm: Cortical and brainstem neurodegeneration associate with the clinical severity in spinocerebellar ataxia patients

D. Tamuli, M. Kaur, S. Kumaran, A. Jaryal, A. Srivastava, K. Deepak (New Delhi, India)

1:45pm-3:15pm: Dissociative effects of thyrotropin releasing hormone on classical cerebellar ataxic signs and cerebellar adaptation in patients with spinocerebellar degeneration

T. Shimizu, R. Hanajima, R. Tsutsumi, N. Tominaga, Y. Ugawa, K. Nishiyama (Sagamihara, Japan)

1:45pm-3:15pm: Electrophysiological characteristics of tremor in spinocerebellar ataxia type12 (SCA-12) and essential tremor (ET)

A. Srivastava, M. Narang, R. Rajan, G. Shukla, F. Mohammad, A. Pandit, D. Vibha, M. Singh, M. Srivastava, K. Prasad (New Delhi, India)

1:45pm-3:15pm: Evaluation of Balance in Hereditary Ataxias

H. Teive, B. Zeigelboim, R. Santos, S. Dias, N. Mello, V. Fonseca (Cuitiba, Brazil)

1:45pm-3:15pm: Fast paced gait may be more discriminating than dual tasking for detecting severity of gait and turn deficits in FXTAS

J. O'Keefe, D. Carnes, E. Robertson, T. Young, N. Purcell, E. Berry-Kravis, D. Hall (Chicago, IL, USA)

1:45pm-3:15pm: FXN and ATXN2 methylation profile in Friedreich’s ataxia and spinocerebellar ataxia type 2

E. Nuzhnyi, N. Abramycheva, T. Pogoda, S. Klyushnikov, M. Ershova, S. Illarioshkin, E. Fedotova (Moscow, Russian Federation)

1:45pm-3:15pm: Genotype-phenotype correlations in 104 Uzbekish families with Spinocerebellar ataxias

F. Rakhimov, Y. Majidova, G. Rakhimbaeva (Tashkent, Uzbekistan)

1:45pm-3:15pm: Gluten sensitivity in progressive cerebellar ataxia patients from India

I. Singh, A. Verma, I. Singh, A. Singh, V. Suroliya, U. Hooda, M. Faruq, V. Ahuja, G. Makharia, A. Srivastava (New Delhi, India)

1:45pm-3:15pm: Hearing Evaluation (Peripheral and Central) in Patients with Sporadic Ataxia

H. Teive, B. Zeigelboim, A. Vom Scheidt, K. Kronbauer, N. Mello, R. Santos (Curitiba, Brazil)

1:45pm-3:15pm: Identification of modifiers of the age of onset variance and disease progression in a Dutch cohort of Machado-Joseph disease patients

M. Huang, V. Leotti, J. Vries, G. Meerman, E. Brunt, C. Bemelmans, H. Kampinga, L. Jardim, D. Verbeek (Groningen, Netherlands)

1:45pm-3:15pm: Influence of disease progression on the quality of life of individuals with spinocerebellar ataxia type 10

L. Santos, M. Zonta, H. Teive, N. Mello, F. Neto, A. Macedo (Curitiba, Brazil)

1:45pm-3:15pm: Intellectual disability with spastic ataxia: Atypical Infantile neuroaxonal dystrophy with absent spheroids

A. Elavarasi, V. Goyal, P. Samal (Puducherry, India)

1:45pm-3:15pm: Intensive speech rehabilitation in degenerative ataxias improves intelligility

A. Vogel, N. Rommel, M. Synofzik (Melbourne, Australia)

1:45pm-3:15pm: Loss of paraplegin drives spasticity rather than ataxia in SPG7: A European cohort analysis of 238 patients

G. Coarelli, R. Schule, B. vande Warrenburg, P. de Jonghe, C. Ewenczyk, A. Martinuzzi, M. Synofzik, E. Hamer, J. Baets, M. Anheim, L. Schöls, T. Deconinck, B. Fontaine, T. Klockgether, MG. D'Angelo, ML. Monin, P. Charles, MT. Bassi, T. Klopstock, E. Ollagnon-Roman, C. Kamm, M. Papin, CS. Davoine, G. Banneau, S. Tezenasdu Montcel, D. Seilhean, A. Brice, C. Duyckaerts, G. Stevanin, A. Durr (Paris, France)

1:45pm-3:15pm: mGluR1 antibodies encephalitis: A rare cause of reversible ataxia and myoclonus syndrome

F. Ory Magne, C. Goillion, J. Dupouy, M. Simonetta, C. Brefel Courbon, O. Rascol, J. (Toulouse, France)

1:45pm-3:15pm: MicroRNAs Unveil Metabolic Imbalance in Spinocerebellar Ataxia Type-2

V. Swarup, R. Singh, H. Singh, I. Singh, M. Faruq, S. Vivekanandhan, A. Srivastava (New Delhi, India)

1:45pm-3:15pm: Motor speech and swallowing phenotype of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)

A. Vogel, N. Rommel, A. Oettinger, L. Stoll, E-M. Kraus, C. Gagnon, P. Krumm, M. Horger, D. Timmann, E. Storey, L. Schöls, M. Synofzik (Melbourne, Australia)

1:45pm-3:15pm: MRI and behavioural account of the aging cerebellum

M. Bares, P. Filip, C. Gallea, S. Lehericy, O. Lungu (Brno, Czech Republic)

1:45pm-3:15pm: Multi-tiered Diagnostic Approaches Reveal a High Degree of Genetic Heterogeneity for Hereditary Cerebellar Ataxias: A Retrospective Review of an Australian Cohort

C. Kang, C. Liang, K. Ahmad, Y. Gu, SF. Siow, J. Colebatch, S. Whyte, K. Ng, P. Cremer, R. Davis, T. Roscioli, M. Cowley, J.S. Park, C. Sue, K. Kumar (Sydney, Australia)

1:45pm-3:15pm: Muscle Ultrasound Comparison Between Early And Intermediate Onset Friedreich’s Ataxia

R. Verbeek, A. Waalkens, M. Kuiper, C. Verschuuren-Bemelmans, J. vd Hoeven, J. de Vries, J. van Gaalen, M. Willemsen, H. Kremer, D. Sival (Groningen, Netherlands)

1:45pm-3:15pm: Non-motor symptoms in Spinocerebellar ataxia, multiple system atrophy and Idiopathic late-onset cerebellar ataxia

YM. Park, MJ. Kim, SB. Koh (Seoul, Republic of Korea)

1:45pm-3:15pm: Novel CACNA1A gene mutation in a Taiwan family with episodic ataxia type 2

KF. Chen, CH. Tsai, DC. Wu (Taichung, Taiwan)

1:45pm-3:15pm: Objective Measures of Ataxic Gait Using Wearable Inertial Sensors

M. El-Gohary, L. Horak, C. Gomez (Portland, OR, USA)

1:45pm-3:15pm: Ocular flutter, generalized myoclonus and ataxia syndrome associated with Human Immunodeficiency Virus: A case report

K. Tan, GB. Eow, A.A. Augustine (George Town, Malaysia)

1:45pm-3:15pm: Open-label pilot trial of citicoline for fragile X-associated tremor/ataxia syndrome (FXTAS)

D. Hall, E. Robertson, M. Leehey, A. McAsey, B. Ouyang, E. Berry-Kravis, J. O'Keefe (Chicago, IL, USA)

1:45pm-3:15pm: Pathophysiologic insights into ataxia and spasticity through structural imaging of a spinocerebellar ataxia type 7 (SCA7) cohort

J. Parker, S. Merchant, S. Horovitz, M. Hallett (Bethesda, MD, USA)

1:45pm-3:15pm: Rapidly progressive ataxia caused by an undetermined paraneoplastic disorder: A case report

J. Conway, A. Feigin (New York, NY, USA)

1:45pm-3:15pm: Rare ADCY6 variants in two families with cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS)

N. Brüggemann, L. Olschewski, V. Tadic, A. Münchau, C. Helmchen, K. Lohmann (Lübeck, Germany)

1:45pm-3:15pm: Recurrent Ataxia in a Young Lady with Hashimoto’s Thyroiditis

I. Sarker, M. Habib, H. Rahman, A. Rizvi (Dhaka, Bangladesh)

1:45pm-3:15pm: Respiratory Complaints in Individuals with Spinocerebelar Ataxia Type 2

N. Mello, H. Teive (Curitiba, Brazil)

1:45pm-3:15pm: Slowly progressive anti-Ca/ARHGAP26 autoantibody-associated cerebellar ataxia over 27 years without immunosuppressive treatment

E. Schegk, I. Beiser, A. Wicki, L. Achtnichts, M. Bertschi (Aarau, Switzerland)

1:45pm-3:15pm: The etiologies of chronic progressive cerebellar ataxia in a Korean population

J. Youn, M. Kim, JH. AHN, JW. Cho, JS. Kim (Seoul, Republic of Korea)

1:45pm-3:15pm: Transcriptional profiling of peripheral blood monocytes from child Friedreich’s ataxia patient: New molecules and patterns of gene expression

H. Singh, V. Swarup, R. Singh, I. Singh, M. Faruq, S. Vivekanandhan, A. Srivastava (Delhi, India)

1:45pm-3:15pm: Treatment with docosahexaenoic acid in Spinocerebellar Ataxia 38

D. Perani, L. Orsi, C. Costanzi, M. Ferrero, A. Zoppo, F. Tempia, D. Caruso, M. Grassi, A. Padovani, A. Brusco, B. Borroni (Brescia, Italy)

1:45pm-3:15pm: Under three seconds: Objective speech markers of ataxia in Multiple Sclerosis

G. Noffs, F. Boonstra, S. Kolbe, A. Evans, H. Butzkeuven, T. Perera, A. Walt, A. Vogel (Melbourne, Australia)

1:45pm-3:15pm: Urinary symptoms and Urodynamic findings in patients with SCAs and DRPLA

M. Jang, A. Kim, B. Jeon, H. Kim (Jeollabuk-do, Republic of Korea)

1:45pm-3:15pm: Urodynamic findings in a cohort of patients with SCA7 reporting lower urinary tract symptoms

T. Uchiyama, J. Ribeiro, P. Giunti, P. Georgopoulos, M. Pakzad, R. Sakakibara, S. Kuwabara, K. Hirata, J. Panicker (Chiba, Japan)

1:45pm-3:15pm: Usefulness of Sway Area for Assessing Balance and Stability in People with Sporadic Adult Onset Cerebellar Ataxia

PW. Ko, YH. Lim, K. Kang, HW. Lee (Daegu, Republic of Korea)

1:45pm-3:15pm: Vestibulo-Ocular Reflex Assessment in Patients with Sporadic Ataxia

H. Teive, B. Zeigelboim, K. Kronbauer, A. Vom Scheidt, R. Santos, N. Mello (Curitiba, Brazil)

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