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Frontiers in Cellular Neuroscience|August 7, 2023
Overexpression of the autism candidate gene <i>Cyfip1</i> pathologically enhances olivo-cerebellar signaling in miceSilas E Busch, Dana H Simmons, Eric Gama, et al.
Cell|July 6, 2013
Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6Xiaofei Du, Jun Wang, Haipeng Zhu, et al.
Annals of Neurology|March 3, 2004
Focal caspase activation underlies the endplate myopathy in slow-channel syndromeBhupinder P S Vohra, Jason S Groshong, Ricardo A Maselli, et al.
Neurorehabilitation and Neural Repair|December 28, 2025
Pre-Frontal Cortical Activity During Gait is Altered in Pre-Manifest and Early Spinocerebellar AtaxiaMartina Mancini, Carla Silva-Batista, Vrutangkumar V Shah, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 23, 2005
Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypesMatthias Maschke, Gary Oehlert, Ting-Dong Xie, et al.
Brain Research|August 18, 2010
(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2Isabelle Iltis, Diane Hutter, Khalaf O Bushara, et al.
Neuroimage|July 18, 2006
Changes in the amplitude and timing of the hemodynamic response associated with prepulse inhibition of acoustic startleMorris B Goldman, Linda Heidinger, Kirti Kulkarni, et al.
Annals of Neurology|December 19, 2003
Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficitsS H Subramony, Kelly Schott, Robert S Raike, et al.
Research Square|May 3, 2023
Intermuscular coherence in spinocerebellar ataxias 3 and 6: a preliminary studyNaoum P Issa, Serdar Aydin, Shail Bhatnagar, et al.
Human Molecular Genetics|May 9, 2015
DnaJ-1 and karyopherin α3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6Wei-Ling Tsou, Ryan R Hosking, Aaron A Burr, et al.
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