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Showing results (41-50 of 46) with videos related to

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BMJ Open|January 12, 2022
Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort studyYu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, et al.
Journal of Neurology|October 17, 2023
Cognitive impairment associated with cerebellar volume loss in spinocerebellar ataxia type 3Zhi-Xian Ye, Jin Bi, Liang-Liang Qiu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2023
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular CharacterizationXiang Lin, Jun-Yi Jiang, Dao-Jun Hong, et al.
Annals of Neurology|June 14, 2022
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal MyopathyYi-Heng Zeng, Kang Yang, Gan-Qin Du, et al.
Journal of Human Genetics|June 12, 2024
Characteristics of tandem repeat inheritance and sympathetic nerve involvement in GAA-FGF14 ataxiaZe-Hong Zheng, Chun-Yan Cao, Bi Cheng, et al.
Annals of Neurology|June 24, 2025
Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral-Pallidoluysian Atrophy PatientsRu-Ying Yuan, Ya-Fang Chen, Wei Lin, et al.
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Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
BMJ Open|January 12, 2022
Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort studyYu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, et al.
Journal of Neurology|October 17, 2023
Cognitive impairment associated with cerebellar volume loss in spinocerebellar ataxia type 3Zhi-Xian Ye, Jin Bi, Liang-Liang Qiu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2023
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular CharacterizationXiang Lin, Jun-Yi Jiang, Dao-Jun Hong, et al.
Annals of Neurology|June 14, 2022
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal MyopathyYi-Heng Zeng, Kang Yang, Gan-Qin Du, et al.
Journal of Human Genetics|June 12, 2024
Characteristics of tandem repeat inheritance and sympathetic nerve involvement in GAA-FGF14 ataxiaZe-Hong Zheng, Chun-Yan Cao, Bi Cheng, et al.
Annals of Neurology|June 24, 2025
Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral-Pallidoluysian Atrophy PatientsRu-Ying Yuan, Ya-Fang Chen, Wei Lin, et al.
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