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E Shan

Showing results (31-40 of 70) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Transient syndrome of continuous muscle fiber activity associated with staphylococcal infectionY C Liu, Z A Wu, S J Wang, et al.
Clinical Neurology and Neurosurgery|March 10, 1998
Genetic screening for Huntington's disease in Chinese patients with involuntary movementsD E Shan, B W Soong, S I Yeh, et al.
European Journal of Neurology|December 4, 2003
SIADH and seizure associated with immunoglobulin therapyC-D Kao, J-T Chen, Z-A Wu, et al.
Parkinsonism & Related Disorders|June 24, 2006
The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairmentI-Sheng Lin, Ruey-Meei Wu, Guey-Jen Lee-Chen, et al.
AJNR. American Journal of Neuroradiology|April 10, 2007
Presence of activated microglia in a high-signal lesion on T1-weighted MR images: a biopsy sample re-examinedDin-E Shan, Hung-Chi Pan, Donald M T Ho, et al.
Clinical Biochemistry|May 27, 2010
Val-9Ala and Ile+58Thr polymorphism of MnSOD in Parkinson's diseaseVinchi Wang, Shao-Yuan Chen, Tzu-Chao Chuang, et al.
Journal of the Chinese Medical Association : JCMA|January 15, 2005
Multiple sclerosis in TaiwanChing-Piao Tsai, Chih-Lun Yuan, Hsiang-Yu Yu, et al.
European Review for Medical and Pharmacological Sciences|May 25, 2017
Mechanism of the high coagulation state of breast cancer tissue factorX-K Mi, Q-R Liu, L Zhu, et al.
Journal of the Neurological Sciences|January 22, 2013
Polymorphic Ala-allele carriers at residue 1170 of HER2 associated with Parkinson's diseaseVinchi Wang, Tzu-Chao Chuang, Ming-Ching Kao, et al.
European Journal of Epidemiology|April 6, 2007
Polymorphism distribution of prion protein codon 117, 129 and 171 in TaiwanKaw-Chen Wang, Vinchi Wang, Ming-Chieh Sun, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Transient syndrome of continuous muscle fiber activity associated with staphylococcal infectionY C Liu, Z A Wu, S J Wang, et al.
Clinical Neurology and Neurosurgery|March 10, 1998
Genetic screening for Huntington's disease in Chinese patients with involuntary movementsD E Shan, B W Soong, S I Yeh, et al.
European Journal of Neurology|December 4, 2003
SIADH and seizure associated with immunoglobulin therapyC-D Kao, J-T Chen, Z-A Wu, et al.
Parkinsonism & Related Disorders|June 24, 2006
The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairmentI-Sheng Lin, Ruey-Meei Wu, Guey-Jen Lee-Chen, et al.
AJNR. American Journal of Neuroradiology|April 10, 2007
Presence of activated microglia in a high-signal lesion on T1-weighted MR images: a biopsy sample re-examinedDin-E Shan, Hung-Chi Pan, Donald M T Ho, et al.
Clinical Biochemistry|May 27, 2010
Val-9Ala and Ile+58Thr polymorphism of MnSOD in Parkinson's diseaseVinchi Wang, Shao-Yuan Chen, Tzu-Chao Chuang, et al.
Journal of the Chinese Medical Association : JCMA|January 15, 2005
Multiple sclerosis in TaiwanChing-Piao Tsai, Chih-Lun Yuan, Hsiang-Yu Yu, et al.
European Review for Medical and Pharmacological Sciences|May 25, 2017
Mechanism of the high coagulation state of breast cancer tissue factorX-K Mi, Q-R Liu, L Zhu, et al.
Journal of the Neurological Sciences|January 22, 2013
Polymorphic Ala-allele carriers at residue 1170 of HER2 associated with Parkinson's diseaseVinchi Wang, Tzu-Chao Chuang, Ming-Ching Kao, et al.
European Journal of Epidemiology|April 6, 2007
Polymorphism distribution of prion protein codon 117, 129 and 171 in TaiwanKaw-Chen Wang, Vinchi Wang, Ming-Chieh Sun, et al.
Pageof 7