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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
November 20, 2015
A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demon
Yu-Wen Cheng, Ming-Jen Lee, Ta-Fu Chen, et al.
Plos One
|
November 4, 2015
The Temporal Profiles of Changes in Nerve Excitability Indices in Familial Amyloid Polyneuropathy
Hsing-Jung Lai, Ya-Wen Chiang, Chih-Chao Yang, et al.
Free Radical Biology & Medicine
|
December 25, 2012
Increase of oxidative stress by a novel PINK1 mutation, P209A
Wei-Lin Chien, Tzeng-Ruei Lee, Shih-Ya Hung, et al.
Neurology. Genetics
|
May 9, 2025
Prevalence and Characteristics of Pathogenic Variants in Taiwanese Patients With Cerebral Small Vessel Disease
Yu-Wen Cheng, Chih-Hao Chen, Ya-Fang Chen, et al.
Parkinsonism & Related Disorders
|
March 6, 2009
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation
Chun-Hwei Tai, Ruoh-Fan Yen, Chin-Hsien Lin, et al.
Pesticide Biochemistry and Physiology
|
April 6, 2024
Biophysical mechanisms underlying tefluthrin-induced modulation of gating changes and resurgent current generation in the human Na<sub>v</sub>1.4 channel
Hsing-Jung Lai, Ming-Jen Lee, Hsin-Wei Yu, et al.
Journal of Alzheimer'S Disease : JAD
|
February 22, 2011
Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease
Ya-Ying Wu, Irene Han-Juo Cheng, Chin-Cheng Lee, et al.
Clinical Chemistry
|
September 18, 2010
The microRNA spectrum in 12 body fluids
Jessica A Weber, David H Baxter, Shile Zhang, et al.
Fertility and Sterility
|
February 6, 2008
Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography
Gwo-Chin Ma, Shuenn-Dyh Chang, Yu Chang, et al.
Plos One
|
January 1, 2015
Soluble AXL: a possible circulating biomarker for neurofibromatosis type 1 related tumor burden
Gunnar Johansson, Po-Chun Peng, Po-Yuan Huang, et al.
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of 9
Search research articles
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Showing results (51-60 of 88) with videos related to
Sort By:
Page
of 9
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
November 20, 2015
A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demon
Yu-Wen Cheng, Ming-Jen Lee, Ta-Fu Chen, et al.
Plos One
|
November 4, 2015
The Temporal Profiles of Changes in Nerve Excitability Indices in Familial Amyloid Polyneuropathy
Hsing-Jung Lai, Ya-Wen Chiang, Chih-Chao Yang, et al.
Free Radical Biology & Medicine
|
December 25, 2012
Increase of oxidative stress by a novel PINK1 mutation, P209A
Wei-Lin Chien, Tzeng-Ruei Lee, Shih-Ya Hung, et al.
Neurology. Genetics
|
May 9, 2025
Prevalence and Characteristics of Pathogenic Variants in Taiwanese Patients With Cerebral Small Vessel Disease
Yu-Wen Cheng, Chih-Hao Chen, Ya-Fang Chen, et al.
Parkinsonism & Related Disorders
|
March 6, 2009
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation
Chun-Hwei Tai, Ruoh-Fan Yen, Chin-Hsien Lin, et al.
Pesticide Biochemistry and Physiology
|
April 6, 2024
Biophysical mechanisms underlying tefluthrin-induced modulation of gating changes and resurgent current generation in the human Na<sub>v</sub>1.4 channel
Hsing-Jung Lai, Ming-Jen Lee, Hsin-Wei Yu, et al.
Journal of Alzheimer'S Disease : JAD
|
February 22, 2011
Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease
Ya-Ying Wu, Irene Han-Juo Cheng, Chin-Cheng Lee, et al.
Clinical Chemistry
|
September 18, 2010
The microRNA spectrum in 12 body fluids
Jessica A Weber, David H Baxter, Shile Zhang, et al.
Fertility and Sterility
|
February 6, 2008
Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography
Gwo-Chin Ma, Shuenn-Dyh Chang, Yu Chang, et al.
Plos One
|
January 1, 2015
Soluble AXL: a possible circulating biomarker for neurofibromatosis type 1 related tumor burden
Gunnar Johansson, Po-Chun Peng, Po-Yuan Huang, et al.
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of 9