Case Report: Familial hypocalciuric hypercalcemia type 1 with a novel mutation combined with Gitelman syndrome and a review of the literatureFRONTIERS IN ENDOCRINOLOGYIF4.62025-02-250OAAI
Functional evaluation of novel compound heterozygous variants in SLC12A3 of Gitelman syndromeORPHANET JOURNAL OF RARE DISEASESIF3.52025-02-111OAAI
Feature Extraction and Applicability Comparisons for Fault Detection of Inter-Turn Short-Circuited PMSMIEEE TRANSACTIONS ON INSTRUMENTATION AND MEASUREMENTIF5.92024-01-011PRE
Application of Phasor Measurement Unit on Locating Disturbance Source for Low-Frequency OscillationIEEE TRANSACTIONS ON SMART GRIDIF9.82010-12-01179PREAI