A Case Report of a 3-Year-Old Child With Anaphylactic Shock After a Diclofenac Suppository Confirmed by Serial Tryptase and a Basophil Activation Test

por Huang, Wun-Yan, Chiu, Tsu-Man, Kuo, Su-Feng, Chung, Wen-Hung, Tsai, Yi-Giien
Publicado 2022

A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review

por Shih, Yu-Hung, Huang, Ying-Chih, Lin, Ching-Yeh, Lin, Hsuan-Yu, Kuo, Su-Feng, Lin, Jen-Shiou, Shen, Ming-Ching
Publicado 2023

Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813(∗) and two variants specific to East Asians

por Lin, Hsuan-Yu, Lin, Ching-Yeh, Kuo, Su-Feng, Lin, Jen-Shiou, Lin, Po-Te, Huang, Ying-Chih, Hsieh, Han-Ni, Shen, Ming-Ching
Publicado 2023

Critical Test Result Recall Supporting System (CTR RSS) Improves Follow-Up among Patients in the Community

por Chang, Hsu-Tung, Kuo, Su-Feng, Chen, Shu-Hui, Lin, Jen-Shiou, Lin, Shu-Hui, Chang, Chin-Fu, Twu, Chih-Wen, Chen, Mei-Chu, Yang, Yuan-Ting, Kor, Chew-Teng, Lin, Ching-Hsiung
Publicado 2022

Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation

por Chou, Sheng-Chieh, Lin, Ching-Yeh, Lin, Hsuan-Yu, Pai, Chen-Hsueh, Yu, Cheng-Ye, Kuo, Su-Feng, Lin, Jen-Shiou, Lin, Po-Te, Hung, Mei-Hua, Hsieh, Han-Ni, Liu, Hsiang-Chun, Shen, Ming-Ching
Publicado 2022