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Neurodegenerative Disease Management|July 28, 2018
Double-blind, randomized and controlled trial of EPI-743 in Friedreich's ataxiaTheresa Zesiewicz, Jason L Salemi, Susan Perlman, et al.
Neurology and Therapy|May 30, 2024
Video-Based Kinematic Analysis of Movement Quality in a Phase 3 Clinical Trial of Troriluzole in Adults with Spinocerebellar Ataxia: A Post Hoc AnalysisGilbert J L'Italien, Evangelos K Oikonomou, Rohan Khera, et al.
Acta Neuropathologica|December 6, 2008
A patient with Huntington's disease and long-surviving fetal neural transplants that developed mass lesionsC Dirk Keene, Rubens C Chang, James B Leverenz, et al.
Cerebellum (London, England)|May 6, 2024
Development and Validation of SCACOMS, a Composite Scale for Assessing Disease Progression and Treatment Effects in Spinocerebellar AtaxiaGilbert L'Italien, Evan Popoff, Basia Rogula, et al.
The Journal of Pediatrics|June 20, 2002
Early diagnosis of ataxia-telangiectasia using radiosensitivity testingXia Sun, Sara G Becker-Catania, Helen H Chun, et al.
Human Molecular Genetics|May 24, 2018
Peripheral blood gene expression reveals an inflammatory transcriptomic signature in Friedreich's ataxia patientsDaniel Nachun, Fuying Gao, Charles Isaacs, et al.
Molecular Cell|September 25, 2010
AID-induced genotoxic stress promotes B cell differentiation in the germinal center via ATM and LKB1 signalingMara H Sherman, Ali I Kuraishy, Chetan Deshpande, et al.
Annals of Clinical and Translational Neurology|September 15, 2017
Impact of diabetes in the Friedreich ataxia clinical outcome measures studyAshley McCormick, Jennifer Farmer, Susan Perlman, et al.
The Journal of Experimental Medicine|June 23, 2010
ATM-deficient thymic lymphoma is associated with aberrant tcrd rearrangement and gene amplificationShan Zha, Craig H Bassing, Takaomi Sanda, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2012
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxiaBrent L Fogel, Ji Yong Lee, Jessica Lane, et al.
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