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Min-Yu Lan

Showing results (1-10 of 86) with videos related to

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Angiology|May 17, 2006
Postural compression of subclavian vein in droopy shoulder syndrome--a case reportMin-Yu Lan, Yung-Yee Chang, Jia-Shou Liu
Movement Disorders Clinical Practice|March 10, 2026
Claval Hypertrophy with Persistent Diffusion Restriction in PLA2G6-Associated NeurodegenerationShih-Chun Lan, Shih-Wei Hsu, Min-Yu Lan
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 18, 2006
Segmental disruption of internal elastic lamina in spontaneous vertebral artery dissection combined with redundancy of multiple cervical arteriesMin-Yu Lan, Yung-Yee Chang, Chao-Cheng Huang, et al.
Cerebellum (London, England)|April 8, 2025
Spinocerebellar Ataxia 44 Caused by a Novel GRM1 Variant: Reviewing the Contrasting Pathogenic Mechanisms Underlying Two GRM1-Associated Hereditary AtaxiasShih-Chun Lan, Yung-Yee Chang, Tsu-Kung Lin, et al.
Blood Cells, Molecules & Diseases|June 17, 2008
A novel 12-base pair deletion mutation in exon 15 of the porphobilinogen deaminase gene in a Taiwanese patient with acute intermittent porphyriaJun-Ichi Sakabe, Shinji Susa, Makoto Daimon, et al.
Stem Cell Research|December 7, 2025
Generation of an induced pluripotent stem cell line (KCGMHi003-A) from a patient with spinocerebellar ataxia type 8 (SCA8)Min-Yu Lan, Sheng-Jye Lim, Huai-En Lu, et al.
Clinical Genetics|November 27, 2025
CHD8-Related Neurodevelopmental Disorder Manifesting Adult-Onset Compulsive BehaviorsShih-Chun Lan, Min-Yu Lan, Yung-Yee Chang, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 26, 2011
An unusual presentation of hypokalemic paralysis with evolving pure motor hemiparesisYan-Ting Lu, Min-Yu Lan, Jia-Shou Liu, et al.
Journal of Clinical Lipidology|August 21, 2022
Spontaneous splenic rupture as the first clinical manifestation of Niemann-Pick disease type B: A case report and review of the literatureMin-Yu Lan, Tsung-Wei Kang, Shih-Chun Lan, et al.
Molecular Biology Reports|May 21, 2025
Phenotypic and molecular characterization of a recurrent SPTAN1 mutation causing SPG91Shih-Chun Lan, Ming-Der Perng, Yung-Yee Chang, et al.
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
Angiology|May 17, 2006
Postural compression of subclavian vein in droopy shoulder syndrome--a case reportMin-Yu Lan, Yung-Yee Chang, Jia-Shou Liu
Movement Disorders Clinical Practice|March 10, 2026
Claval Hypertrophy with Persistent Diffusion Restriction in PLA2G6-Associated NeurodegenerationShih-Chun Lan, Shih-Wei Hsu, Min-Yu Lan
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 18, 2006
Segmental disruption of internal elastic lamina in spontaneous vertebral artery dissection combined with redundancy of multiple cervical arteriesMin-Yu Lan, Yung-Yee Chang, Chao-Cheng Huang, et al.
Cerebellum (London, England)|April 8, 2025
Spinocerebellar Ataxia 44 Caused by a Novel GRM1 Variant: Reviewing the Contrasting Pathogenic Mechanisms Underlying Two GRM1-Associated Hereditary AtaxiasShih-Chun Lan, Yung-Yee Chang, Tsu-Kung Lin, et al.
Blood Cells, Molecules & Diseases|June 17, 2008
A novel 12-base pair deletion mutation in exon 15 of the porphobilinogen deaminase gene in a Taiwanese patient with acute intermittent porphyriaJun-Ichi Sakabe, Shinji Susa, Makoto Daimon, et al.
Stem Cell Research|December 7, 2025
Generation of an induced pluripotent stem cell line (KCGMHi003-A) from a patient with spinocerebellar ataxia type 8 (SCA8)Min-Yu Lan, Sheng-Jye Lim, Huai-En Lu, et al.
Clinical Genetics|November 27, 2025
CHD8-Related Neurodevelopmental Disorder Manifesting Adult-Onset Compulsive BehaviorsShih-Chun Lan, Min-Yu Lan, Yung-Yee Chang, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 26, 2011
An unusual presentation of hypokalemic paralysis with evolving pure motor hemiparesisYan-Ting Lu, Min-Yu Lan, Jia-Shou Liu, et al.
Journal of Clinical Lipidology|August 21, 2022
Spontaneous splenic rupture as the first clinical manifestation of Niemann-Pick disease type B: A case report and review of the literatureMin-Yu Lan, Tsung-Wei Kang, Shih-Chun Lan, et al.
Molecular Biology Reports|May 21, 2025
Phenotypic and molecular characterization of a recurrent SPTAN1 mutation causing SPG91Shih-Chun Lan, Ming-Der Perng, Yung-Yee Chang, et al.
Pageof 9