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Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
September 16, 2019
Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser
Hsing-Jung Lai, Kuan-Chih Huang, Yun-Chieh Liang, et al.
Plos One
|
August 15, 2017
Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutation
Xiang-Jun Sheng, Hunag-Ju Tu, Wei-Lin Chien, et al.
Brain : a Journal of Neurology
|
August 2, 2008
Nerve function and dysfunction in acute intermittent porphyria
Cindy S-Y Lin, Arun V Krishnan, Ming-Jen Lee, et al.
European Neurology
|
October 12, 2011
Neurological complications of acute intermittent porphyria
Hung-Chou Kuo, Chin-Chang Huang, Chun-Che Chu, et al.
European Journal of Neurology
|
July 5, 2022
Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhage
Chih-Hao Chen, Yung-Tsai Chu, Ya-Fang Chen, et al.
Journal of Inherited Metabolic Disease
|
September 7, 2022
EXPLORE B: A prospective, long-term natural history study of patients with acute hepatic porphyria with chronic symptoms
David Cassiman, Raili Kauppinen, Susana Monroy, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
March 28, 2024
Patisiran, an RNAi therapeutic for hereditary transthyretin-mediated amyloidosis: Sub-analysis in Taiwanese patients from the APOLLO study
Kon-Ping Lin, Chih-Chao Yang, Yi-Chung Lee, et al.
Plos One
|
August 8, 2012
PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort
Yi-Chung Lee, Ming-Jen Lee, Hsiang-Yu Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 14, 2008
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism
Ming-Jen Lee, Ignacio F Mata, Chin-Hsien Lin, et al.
JACC. Cardiovascular Imaging
|
March 7, 2023
Tafamidis Treatment Decreases <sup>99m</sup>Tc-Pyrophosphate Uptake in Patients With Hereditary Ala97Ser Transthyretin Amyloid Cardiomyopathy
An-Li Yu, Yi-Chieh Chen, Cheng-Hsuan Tsai, et al.
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Search research articles
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Showing results (61-70 of 88) with videos related to
Sort By:
Page
of 9
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
September 16, 2019
Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser
Hsing-Jung Lai, Kuan-Chih Huang, Yun-Chieh Liang, et al.
Plos One
|
August 15, 2017
Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutation
Xiang-Jun Sheng, Hunag-Ju Tu, Wei-Lin Chien, et al.
Brain : a Journal of Neurology
|
August 2, 2008
Nerve function and dysfunction in acute intermittent porphyria
Cindy S-Y Lin, Arun V Krishnan, Ming-Jen Lee, et al.
European Neurology
|
October 12, 2011
Neurological complications of acute intermittent porphyria
Hung-Chou Kuo, Chin-Chang Huang, Chun-Che Chu, et al.
European Journal of Neurology
|
July 5, 2022
Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhage
Chih-Hao Chen, Yung-Tsai Chu, Ya-Fang Chen, et al.
Journal of Inherited Metabolic Disease
|
September 7, 2022
EXPLORE B: A prospective, long-term natural history study of patients with acute hepatic porphyria with chronic symptoms
David Cassiman, Raili Kauppinen, Susana Monroy, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
March 28, 2024
Patisiran, an RNAi therapeutic for hereditary transthyretin-mediated amyloidosis: Sub-analysis in Taiwanese patients from the APOLLO study
Kon-Ping Lin, Chih-Chao Yang, Yi-Chung Lee, et al.
Plos One
|
August 8, 2012
PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort
Yi-Chung Lee, Ming-Jen Lee, Hsiang-Yu Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 14, 2008
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism
Ming-Jen Lee, Ignacio F Mata, Chin-Hsien Lin, et al.
JACC. Cardiovascular Imaging
|
March 7, 2023
Tafamidis Treatment Decreases <sup>99m</sup>Tc-Pyrophosphate Uptake in Patients With Hereditary Ala97Ser Transthyretin Amyloid Cardiomyopathy
An-Li Yu, Yi-Chieh Chen, Cheng-Hsuan Tsai, et al.
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of 9