Development of Research on Huntington Disease in China
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Physiology,General Neuroscience
Link
http://link.springer.com/article/10.1007/s12264-016-0093-y/fulltext.html
Reference27 articles.
1. Ross CA, Tabrizi SJ. Huntington’s disease: from molecular pathogenesis to clinical treatment. Lancet Neurol 2011, 10: 83–98.
2. Vonsattel JP, Myers RH, Stevens TJ, Ferrante RJ, Bird ED, Richardson EP, Jr. Neuropathological classification of Huntington’s disease. J Neuropathol Exp Neurol 1985, 44: 559–577.
3. Huntington G. On chorea. J Neuropsychiatry Clin Neurosci 2003, 15: 109–112.
4. Pringsheim T, Wiltshire K, Day L, Dykeman J, Steeves T, Jette N. The incidence and prevalence of Huntington’s disease: a systematic review and meta-analysis. Mov Disord 2012, 27: 1083–1091.
5. Wang ZX. Huntington Disease: 2 cases report. Chin J Nerv Ment Dis 1959, 5: 384–385.
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1. Loss of CAA interruption and intergenerational CAG instability in Chinese patients with Huntington’s disease;Journal of Molecular Medicine;2023-05-26
2. The Chinese Version of UHDRS in Huntington’s Disease: Reliability and Validity Assessment;Journal of Huntington's Disease;2022-12-16
3. Local and Global Abnormalities in Pre-symptomatic Huntington’s Disease Revealed by 7T Resting-state Functional MRI;Neuroscience Bulletin;2022-08-29
4. Gedunin Degrades Aggregates of Mutant Huntingtin Protein and Intranuclear Inclusions via the Proteasomal Pathway in Neurons and Fibroblasts from Patients with Huntington’s Disease;Neuroscience Bulletin;2019-08-20
5. Effect of Apolipoprotein E Genotypes on Huntington’s Disease Phenotypes in a Han Chinese Population;Neuroscience Bulletin;2019-03-18
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