Hsing‐Jung Lai

Mitochondrial <i>UQCRC1</i> mutations cause autosomal dominant parkinsonism with polyneuropathy

Chin‐Hsien Lin, Pei-I Tsai, Han‐Yi Lin et al. · Brain · 2020 · 77 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser

Hsing‐Jung Lai, Kuan‐Chih Huang, Yun‐Chieh Liang et al. · Journal of the Formosan Medical Association · 2019 · 25 citations · Full text

Medicine, Cardiology, Genetics +13

Frail phenotype is associated with distinct quantitative electroencephalographic findings among end-stage renal disease patients: an observational study

Chia‐Ter Chao, Hsing‐Jung Lai, Hung‐Bin Tsai et al. · BMC Geriatrics · 2017 · 16 citations · Full text

Medicine, Geriatric Medicine, Nephrology +17

The Temporal Profiles of Changes in Nerve Excitability Indices in Familial Amyloid Polyneuropathy

Hsing‐Jung Lai, Ya-Wen Chiang, Chih‐Chao Yang et al. · PLoS ONE · 2015 · 14 citations · Full text

Medicine, Neurology, Neuroscience +14

The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited Erythromelalgia

Chiung-Wei Huang, Hsing‐Jung Lai, Po-Yuan Huang et al. · PLoS Biology · 2016 · 14 citations · Full text

Natural Sciences, Biophysics, Physiology +17