Featured
-
-
Article
| Open Access
Clinical value of vestibulo-ocular reflex in the differentiation of spinocerebellar ataxias
- Jae-Myung Kim
- , Tai-Seung Nam
- & Seung-Han Lee
-
Article
| Open Access
Excessive excitability of inhibitory cortical circuit and disturbance of ballistic targeting movement in degenerative cerebellar ataxia
- Akiyoshi Matsugi
- , Satoru Nishishita
- & Koichi Hosomi
-
Article
| Open Access
β-III-spectrin N-terminus is required for high-affinity actin binding and SCA5 neurotoxicity
- Sarah A. Denha
- , Alexandra E. Atang
- & Adam W. Avery
-
Article
| Open Access
Neuropeptide Y (NPY) intranasal delivery alleviates Machado–Joseph disease
- Joana Duarte-Neves
- , Cláudia Cavadas
- & Luís Pereira de Almeida
-
Article
| Open Access
Accurate detection of cerebellar smooth pursuit eye movement abnormalities via mobile phone video and machine learning
- Zhuoqing Chang
- , Ziyu Chen
- & Anoopum S. Gupta
-
Article
| Open AccessExpanding the genotype–phenotype correlation of childhood sensory polyneuropathy of genetic origin
- Samya Chakravorty
- , Rachel Logan
- & Sumit Verma
-
Article
| Open Access
Primary proprioceptive neurons from human induced pluripotent stem cells: a cell model for afferent ataxias
- Chiara Dionisi
- , Myriam Rai
- & Massimo Pandolfo
-
Article
| Open Access
Hippocampal mitochondrial dysfunction and psychiatric-relevant behavioral deficits in spinocerebellar ataxia 1 mouse model
- Filip Tichanek
- , Martina Salomova
- & Jan Cendelin
-
Article
| Open Access
Differential value of brain magnetic resonance imaging in multiple system atrophy cerebellar phenotype and spinocerebellar ataxias
- Minkyeong Kim
- , Jong Hyeon Ahn
- & Jin Whan Cho
-
Article
| Open Access
Fat cadherins in mouse models of degenerative ataxias
- Olga Baron
- , Denise Grieshober
- & Manolis Fanto
-
Article
| Open Access
Functional Transcriptome Analysis in ARSACS KO Cell Model Reveals a Role of Sacsin in Autophagy
- Federica Morani
- , Stefano Doccini
- & Filippo Maria Santorelli
-
Article
| Open Access
Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
- Ching-Yu Chuang
- , Chih-Chao Yang
- & Hung-Chih Kuo
-
Article
| Open Access
A randomized controlled pilot trial of game-based training in individuals with spinocerebellar ataxia type 3
- Ray-Yau Wang
- , Fang-Yi Huang
- & Yea-Ru Yang
-
Article
| Open Access
Elavl3 is essential for the maintenance of Purkinje neuron axons
- Yuki Ogawa
- , Kyoko Kakumoto
- & Hirotaka James Okano
-
Article
| Open Access
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein
- L. L. Mariani
- , S. Rivaud-Péchoux
- & M. Anheim
-
Article
| Open Access
Treatment with Caffeic Acid and Resveratrol Alleviates Oxidative Stress Induced Neurotoxicity in Cell and Drosophila Models of Spinocerebellar Ataxia Type3
- Yu-Ling Wu
- , Jui-Chih Chang
- & Kai-Li Liu
-
Article
| Open Access
Sensorimotor adaptation as a behavioural biomarker of early spinocerebellar ataxia type 6
- Muriel T. N. Panouillères
- , Raed A. Joundi
- & Ned Jenkinson
-
Article
| Open Access
4-aminopyridine reverses ataxia and cerebellar firing deficiency in a mouse model of spinocerebellar ataxia type 6
- Sriram Jayabal
- , Hui Ho Vanessa Chang
- & Alanna J. Watt
-
Article
| Open Access
A human β-III-spectrin spinocerebellar ataxia type 5 mutation causes high-affinity F-actin binding
- Adam W. Avery
- , Jonathan Crain
- & Thomas S. Hays
-
Article
| Open Access
Spinocerebellar ataxia type 21 exists in the Chinese Han population
- Sheng Zeng
- , Junsheng Zeng
- & Junling Wang
-
Article
| Open Access
Abnormalities in synaptic dynamics during development in a mouse model of spinocerebellar ataxia type 1
- Yusuke Hatanaka
- , Kei Watase
- & Yoshitaka Nagai
-
Article
| Open Access
Nuclear retention of full-length HTT RNA is mediated by splicing factors MBNL1 and U2AF65
- Xin Sun
- , Pan P. Li
- & Dobrila D. Rudnicki
-
Article
| Open Access
Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation
- Hiroshi Doi
- , Masao Ushiyama
- & Kunihiro Yoshida
Graft-derived neurons and bystander effects are maintained for six months after human iPSC-derived NESC transplantation in mice’s cerebella