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Human Mutation
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July 13, 2006
Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1
Ming-Jen Lee, Yi-Ning Su, Huey-Ling You, et al.
Clinical Neurology and Neurosurgery
|
March 21, 2008
Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese
Shyue-Ru Chen, Kon-Ping Lin, Hung-Chou Kuo, et al.
Annals of Neurology
|
May 15, 2015
Sudomotor innervation in transthyretin amyloid neuropathy: Pathology and functional correlates
Chi-Chao Chao, Cho-Min Huang, Hao-Hua Chiang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 13, 2018
Detrimental effects of intracerebral haemorrhage on patients with CADASIL harbouring NOTCH3 R544C mutation
Chih-Hao Chen, Sung-Chun Tang, Yu-Wen Cheng, et al.
Orphanet Journal of Rare Diseases
|
May 24, 2024
Unique clinical and electrophysiological features in the peripheral nerve system in patients with sialidosis - a case series study
Sung-Ju Hsueh, Chin-Hsien Lin, Ni-Chung Lee, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
January 12, 2025
Impact of Tafamidis on [<sup>99m</sup>Tc]Tc-pyrophosphate Scintigraphy in Ala97Ser Hereditary Transthyretin amyloid cardiomyopathy: significant initial reduction with stable Long-Term effects
An-Li Yu, Yi-Chieh Chen, Cheng-Hsuan Tsai, et al.
Human Molecular Genetics
|
July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene
Ming-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.
Plos One
|
November 20, 2009
Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus
Ming-Jen Lee, Ching-Pang Chang, Yi-Hsin Lee, et al.
Orphanet Journal of Rare Diseases
|
September 13, 2023
Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study
Cheng-Hsuan Tsai, Chi-Chao Chao, Sung-Tsang Hsieh, et al.
Acta Cardiologica Sinica
|
July 17, 2023
Efficacy of Tafamidis in Patients with Ala97Ser Hereditary Transthyretin Cardiac Amyloidosis: A Six-Month Follow-Up Study
Cheng-Hsuan Tsai, An-Li Yu, Yuan-Kun Aden Wu, et al.
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of 9
Search research articles
Search
Showing results (71-80 of 88) with videos related to
Sort By:
Page
of 9
Human Mutation
|
July 13, 2006
Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1
Ming-Jen Lee, Yi-Ning Su, Huey-Ling You, et al.
Clinical Neurology and Neurosurgery
|
March 21, 2008
Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese
Shyue-Ru Chen, Kon-Ping Lin, Hung-Chou Kuo, et al.
Annals of Neurology
|
May 15, 2015
Sudomotor innervation in transthyretin amyloid neuropathy: Pathology and functional correlates
Chi-Chao Chao, Cho-Min Huang, Hao-Hua Chiang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 13, 2018
Detrimental effects of intracerebral haemorrhage on patients with CADASIL harbouring NOTCH3 R544C mutation
Chih-Hao Chen, Sung-Chun Tang, Yu-Wen Cheng, et al.
Orphanet Journal of Rare Diseases
|
May 24, 2024
Unique clinical and electrophysiological features in the peripheral nerve system in patients with sialidosis - a case series study
Sung-Ju Hsueh, Chin-Hsien Lin, Ni-Chung Lee, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
January 12, 2025
Impact of Tafamidis on [<sup>99m</sup>Tc]Tc-pyrophosphate Scintigraphy in Ala97Ser Hereditary Transthyretin amyloid cardiomyopathy: significant initial reduction with stable Long-Term effects
An-Li Yu, Yi-Chieh Chen, Cheng-Hsuan Tsai, et al.
Human Molecular Genetics
|
July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene
Ming-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.
Plos One
|
November 20, 2009
Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus
Ming-Jen Lee, Ching-Pang Chang, Yi-Hsin Lee, et al.
Orphanet Journal of Rare Diseases
|
September 13, 2023
Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study
Cheng-Hsuan Tsai, Chi-Chao Chao, Sung-Tsang Hsieh, et al.
Acta Cardiologica Sinica
|
July 17, 2023
Efficacy of Tafamidis in Patients with Ala97Ser Hereditary Transthyretin Cardiac Amyloidosis: A Six-Month Follow-Up Study
Cheng-Hsuan Tsai, An-Li Yu, Yuan-Kun Aden Wu, et al.
Page
of 9