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Weiyi Mu

Showing results (21-30 of 48) with videos related to

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Journal of Genetic Counseling|July 10, 2023
The lived experience of reconstructing identity in response to genetic risk of frontotemporal degeneration and amyotrophic lateral sclerosisLaynie Dratch, Jill Owczarzak, Weiyi Mu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2017
Characterization of pulmonary arteriovenous malformations in ACVRL1 versus ENG mutation carriers in hereditary hemorrhagic telangiectasiaWeiyi Mu, Zachary A Cordner, Kevin Yuqi Wang, et al.
SSM. Qualitative Research in Health|June 10, 2026
USING METAPHOR ANALYSIS TO UNDERSTAND PERSONAL AND FAMILIAL EXPERIENCES WITH BEHAVIORAL VARIANT FRONTOTEMPORAL DEMENTIAMakenna May, Ying Zhang, Laynie Dratch, et al.
Clinical Parkinsonism & Related Disorders|August 16, 2023
A case of familial frontotemporal dementia caused by a progranulin gene mutationLauryn Currens, Nigel Harrison, Maria Schmidt, et al.
The Science of the Total Environment|December 13, 2023
Application of carboxymethyl cellulose sodium (CMCNa) in maize-wheat cropping system (MWCS) in coastal saline-alkali soilGe Li, Yuyang Shan, Weibo Nie, et al.
Cerebellum (London, England)|September 4, 2025
Ocular Motor and Vestibular Profile in Spinocerebellar Ataxia Type 27B: Toward a Practical Bedside Diagnostic FrameworkLeonardo Eleuterio Ariello, Daniel R Gold, Weiyi Mu, et al.
Journal of Neurology|October 7, 2025
Video head impulse test differentiates RFC1-CANVAS, FGF14-SCA27B, and idiopathic late-onset cerebellar ataxiasLeonardo E Ariello, Daniel R Gold, Jennifer L Millar, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|July 22, 2025
Causes of Diplopia, Strabismus Patterns, and Ocular Motor Features in Patients With Spinocerebellar Ataxia Type 27BDaniel R Gold, Anand K Bery, Emile Moukheiber, et al.
Annals of Clinical and Translational Neurology|August 30, 2025
Practice Recommendations for Genetic Testing of AtaxiasSharan R Srinivasan, Amy D Mook, Michelle Rochman, et al.
Epilepsia|December 11, 2021
Genetic testing for the epilepsies: A systematic reviewBeth R Sheidley, Jennifer Malinowski, Amanda L Bergner, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Journal of Genetic Counseling|July 10, 2023
The lived experience of reconstructing identity in response to genetic risk of frontotemporal degeneration and amyotrophic lateral sclerosisLaynie Dratch, Jill Owczarzak, Weiyi Mu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2017
Characterization of pulmonary arteriovenous malformations in ACVRL1 versus ENG mutation carriers in hereditary hemorrhagic telangiectasiaWeiyi Mu, Zachary A Cordner, Kevin Yuqi Wang, et al.
SSM. Qualitative Research in Health|June 10, 2026
USING METAPHOR ANALYSIS TO UNDERSTAND PERSONAL AND FAMILIAL EXPERIENCES WITH BEHAVIORAL VARIANT FRONTOTEMPORAL DEMENTIAMakenna May, Ying Zhang, Laynie Dratch, et al.
Clinical Parkinsonism & Related Disorders|August 16, 2023
A case of familial frontotemporal dementia caused by a progranulin gene mutationLauryn Currens, Nigel Harrison, Maria Schmidt, et al.
The Science of the Total Environment|December 13, 2023
Application of carboxymethyl cellulose sodium (CMCNa) in maize-wheat cropping system (MWCS) in coastal saline-alkali soilGe Li, Yuyang Shan, Weibo Nie, et al.
Cerebellum (London, England)|September 4, 2025
Ocular Motor and Vestibular Profile in Spinocerebellar Ataxia Type 27B: Toward a Practical Bedside Diagnostic FrameworkLeonardo Eleuterio Ariello, Daniel R Gold, Weiyi Mu, et al.
Journal of Neurology|October 7, 2025
Video head impulse test differentiates RFC1-CANVAS, FGF14-SCA27B, and idiopathic late-onset cerebellar ataxiasLeonardo E Ariello, Daniel R Gold, Jennifer L Millar, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|July 22, 2025
Causes of Diplopia, Strabismus Patterns, and Ocular Motor Features in Patients With Spinocerebellar Ataxia Type 27BDaniel R Gold, Anand K Bery, Emile Moukheiber, et al.
Annals of Clinical and Translational Neurology|August 30, 2025
Practice Recommendations for Genetic Testing of AtaxiasSharan R Srinivasan, Amy D Mook, Michelle Rochman, et al.
Epilepsia|December 11, 2021
Genetic testing for the epilepsies: A systematic reviewBeth R Sheidley, Jennifer Malinowski, Amanda L Bergner, et al.
Pageof 5