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 · 72 citations · Full text

Sporadic Parkinson, Genetics, Genetic Epidemiology +16

β-Adrenergic modulation of arrhythmogenesis and identification of targeted sites of antiarrhythmic therapy in Timothy (LQT8) syndrome: a theoretical study

Ruey J. Sung, Yung-Han Wu, Hsing‐Jung Lai et al. · American Journal of Physiology-Heart and Circulatory Physiology · 2009 · 23 citations

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 · 20 citations · Full text

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

Neurological Disorder, Neurophysiological Biomarkers, Neurochemical Biomarkers +18

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

Inherited Erythromelalgia, Molecular Pathogenesis, Genetics +28