MDS Virtual Congress 2021 » Ataxia

A case of GAD ataxia and stiff leg syndrome

S. Kalampokini, A. Artemiadis, P. Zis, P. Bargiotas, G. Hadjigeorgiou (Nicosia, Cyprus)

A novel GRM1 variant associated with autosomal dominant cerebellar ataxia (ADCA)

A. Boddu, D. Standaert (Birmingham, USA)

Acute cerebellar ataxia as a possible post-COVID-19 manifestation – case report

B. Ciopleiaș, R. Makk, M. Chioașcă, D. Rusu, ș. Diaconu, L. Irincu, C. Falup-Pecurariu (Brasov, Romania)

Amyotrophic Lateral Sclerosis with SOD1 mutation presenting with progressive cerebellar ataxia

M. Sequeira, P. Faustino, J. Lourenço (Lisboa, Portugal)

Ataxia in a Puerto Rican woman with a missense variant in the CCDC88 gene

C. Serrano, J. Abreu, J. Otero (San Juan, Puerto Rico)

Atypical presentation of Ataxia telangiectasia masquerading as Parkinson’s Disease

G. Casinelli, R. Tripathi (Morgantown, USA)

Autosomal recessive spinocerebellar ataxia type 10: a case report in Mexico

D. Gasca Saldaña, D. Dávila Ortiz, N. Monroy Jaramillo, C. Aláez-Verson, L. Flores-Lagunes, P. Zamora Alaniz, C. Dehesa Caballero, C. Fresno Rodríguez, G. Vega-Rosas, M. Boll (Mexico City, Mexico)

Cerebellar atrophy secondary to lithium intoxication : about 2 cases

M. Fall (Dakar, Senegal)

CEREBELLAR COGNITIVE AFFECTIVE SYNDROME IN SPINOCEREBELLAR ATAXIA TYPE 3

KH. Yap, S. Azmin, SH. Mat Desa, HN. Achok, N. Mohamed Ibrahim (Cheras, Malaysia)

Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile-X Associated Tremor/Ataxia Syndrome

D. Abbasi, T. Nguyen, E. Robertson-Dick, E. Berry-Kravis, S. Cologna, D. Hall (Chicago, USA)

Clinical and imaging features of idiopathic cerebellar ataxia with anti-cerebellar antibodies

A. Takekoshi, A. Kimura, N. Yoshikura, T. Shimohata (Gifu, Japan)

Clinical phenotype and biomarkers in sporadic degenerative ataxia: longitudinal data from the SPORTAX registry

D. önder, C. Wilke, J. Faber, T. Schaprian, I. Giordano, M. Grobe-Einsler, L. Schöls, S. Vielhaber, J. Machts, C. Kamm, A. Dudesek, T. Klopstock, C. Stendel, D. Timmann-Braun, S. Boesch, A. Eigentler, B. van Dewarrenburg, J. van Gaalen, C. Tallaksen, I. Wedding, A. Filla, G. Silvestri, M. Masciullo, C. Ganos, J. Kang, D. Sarah, M. Synofzik, T. Klockgether (Bonn, Germany)

Clinical presentation of coexistence of Spinocerebellar ataxia (SCA14) gene duplication variant in association with Spinocerebellar Ataxia (SCA8) gene mutation in a same patient.

A. Ahmed (Winter Park, USA)

Data-driven model of dynamic biomarkers in SCA3 – from early pre-ataxic to late ataxic disease stages

J. Faber, T. Schaprian, C. Wilke, J. Huebener-Schmid, O. Riess, H. Garcia-Moreno, P. Giunti, B. Vande Warrenburg, J. van Gaalen, M. Lima, M. Raposo, L. Pereira, M. Santana, L. Schoels, J. de Vries, J. Infante, H. Jacobi, D. Timmann-Braun, K. Reetz, M. Schmid, T. Klockgether (Bonn, Germany)

Distinct impulsive traits in cerebellar ataxia and Parkinson’s disease

T. Chen, C. Lin, M. Aumann, D. Claassen, S. Kuo (New York, USA)

EATING HABITS AND NUTRITIONAL STATUS OF PATIENTS WITH HEREDITARY ATAXIAS IN A NORTHEAST BRAZILIAN POPULATION

CGM. Carvalho, SSO. Scott, DM. Rangel, DMS. Soares, PBN. Neto (Fortaleza, Brazil)

Evolution of disability in spinocerebellar ataxias type 1, 2, 3, and 6

H. Jacobi, T. Schaprian, J. Beyersmann, S. Tezenas, T. Klockgether (Heidelberg, Germany)

Extracerebellar Signs and Symptoms in 117 Korean Patients with Early-Stage Spinocerebellar Ataxia

M. Kim, JH. Ahn, JK. Mun, EH. Choi, JS. Kim, J. Youn, JW. Cho (Jinju, Republic of Korea)

Gluten-induced ataxia: a misdiagnosed cause of sporadic ataxia. A case report

R. Zouari, M. Messelmani, M. Mansour, H. Derbali, A. Riahi, I. Bedoui, J. Zaouali, R. Mrissa (Tunis, Tunisia)

Hot cross bun sign in progressive ataxia with ELVOL4 mutation

M. Moreno-Escobar, R. Tripathi (Morgantown, USA)

Immune-Mediated and Mercury Intoxication Ataxias: Anti-GAD Antibodies and Dynamic Stabilometriс Assessment

N. Kolmykova, S. Kiryukhina, D. Labunskiy, E. Razgadova, M. Kustov (Saransk, Russian Federation)

Pain and Non-Motor Symptoms in FXTAS

Y. Bronstein, N. Ashikian, M. Petrovic, A. Shah, I. Romanenko (Woodland Hills, USA)

Phenotype characteristics of ANO10 mutation carries: a case series from Serbia and a systematic review of the literature

I. Stankovic, N. Dragasevic, A. Milovanovic, AA. Marjanovic, M. Brankovic, V. Dobricic, I. Petrovic, M. Svetel, I. Novakovic, V. Kostic (Belgrade, Serbia)

Phenotype-genotype correlation in a case series from South Spain of Hereditary Spastic Paraplegia 7 (SPG7)

A. Adarmes Gómez, S. Jesús Maestre, D. Macias Garcia, L. Muñóz, F. Carrillo Garcia, M. Gómez Garré, P. Mir (Seville, Spain)

Prevalence and Clinical Characteristics of Autosomal Dominant Spinocerebellar Ataxia in a Large Canadian Cohort from Ontario

R. Munhoz, E. Slow, S. Alshimemeri (Toronto, Canada)

Role of Uric Acid in Friedreich Ataxia neurodegeneration

A. Trinchillo, A. de Rosa, F. Saccà (Naples, Italy)

Spinocerebellar ataxia (SCA) type 2 and type 8: a tale of two repeat expansions in a single patient

J. Frey, T. Tholanikunnel, L. Kugelmann, M. Burns, S. Subramony (Gainesville, USA)

Theory of mind in patients with cerebellar neurodegenerative disorders

O. Tamas, A. Kacar, E. Stefanova, B. Salak Djokic, A. Milovanovic, D. Stanisavljevic, M. Kostic, N. Dragasevic Miskovic (Belgrade, Serbia)